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Disease on EC 3.2.1.108 - lactase

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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Acne Vulgaris
Lactase Persistence, Milk Intake, and Adult Acne: A Mendelian Randomization Study of 20,416 Danish Adults.
Acquired Immunodeficiency Syndrome
Review article: the treatment of lactose intolerance.
Acrodermatitis
Morphometric study of the jejunal mucosa in various childhood enteropathies with special reference to intraepithelial lymphocytes.
Acute Kidney Injury
Predictors for postoperative renal function after open partial nephrectomy: Including postoperative biomarkers.
alpha,alpha-trehalase deficiency
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
Possibilities for the cytochemical diagnosis of enzymopathies.
alpha-glucosidase deficiency
Disaccharidase activity in children undergoing esophagogastroduodenoscopy: A systematic review.
Patients with functional bowel disorder have disaccharidase deficiency: A single-center study from Russia.
Selective alteration of brush-border hydrolases in intestinal diseases in childhood.
[Disaccharidase deficiency and functional bowel diseases].
Amyotrophic Lateral Sclerosis
De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes.
Anaphylaxis
Anaphylaxis to supplemental oral lactase enzyme.
Anemia
Autoimmune Hemolytic Anemia Triggered by Infection with Human Parvovirus B19 after Total Abdominal Colectomy for Ulcerative Colitis.
Detecting and Characterizing Genomic Signatures of Positive Selection in Global Populations.
Prognostic value of C-reactive protein, lactase dehydrogenase and anemia in recurrent or refractory aggressive lymphoma.
Anemia, Hemolytic, Autoimmune
Autoimmune Hemolytic Anemia Triggered by Infection with Human Parvovirus B19 after Total Abdominal Colectomy for Ulcerative Colitis.
Anemia, Pernicious
Selected disorders of malabsorption.
Anemia, Sickle Cell
Detecting and Characterizing Genomic Signatures of Positive Selection in Global Populations.
Arthritis, Rheumatoid
Adult T-cell Leukemia/Lymphoma as a Methotrexate-associated Lymphoproliferative Disorder in a Patient with Rheumatoid Arthritis - A Case Report.
Ascariasis
Some experimental approaches to the study of nutrition and parasitic infection.
Asthma
Colonic mucosal eosinophilia in children without inflammatory bowel disease.
Congenital lymphangiectasia and atopy.
Occupational sensitization to lactase in the dietary supplement industry.
beta-fructofuranosidase deficiency
Congenital maltase-glucoamylase deficiency associated with lactase and sucrase deficiencies.
Disaccharidase activity in children undergoing esophagogastroduodenoscopy: A systematic review.
Interaction between dietary carbohydrates and intestinal disaccharidases in experimental diarrhea.
Patients with functional bowel disorder have disaccharidase deficiency: A single-center study from Russia.
Sucrase deficiency in Greenland. Incidence and genetic aspects.
The prevalence and severity of intestinal disaccharidase deficiency in human immunodeficiency virus-infected subjects.
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
Biliary Dyskinesia
What is behind dyspepsia?
Bone Diseases, Metabolic
Lactase deficiency: prevalence in osteoporosis.
Metabolic bone disease as a result of lactase deficiency.
Breast Neoplasms
Breast cancer mortality and diet in the United States.
Carcinoma
Can lactase persistence genotype be used to reassess the relationship between renal cell carcinoma and milk drinking? Potentials and problems in the application of Mendelian randomization.
Influence of remote cancer and obesity on, and distribution of mucosal enzymes in, the upper small intestine.
Lactase persistence and ovarian carcinoma risk in Finland, Poland and Sweden.
Lactase persistence, dietary intake of milk, and the risk for prostate cancer in Sweden and Finland.
[Tumor markers in renal cell carcinoma]
Carcinoma, Renal Cell
Can lactase persistence genotype be used to reassess the relationship between renal cell carcinoma and milk drinking? Potentials and problems in the application of Mendelian randomization.
[Tumor markers in renal cell carcinoma]
Cardiovascular Diseases
Association of the Lactase Persistence Haplotype Block With Disease Risk in Populations of European Descent.
Inhibitory effects of estrogens on digestive enzymes, insulin deficiency, and pancreas toxicity in diabetic rats.
Cataract
A geographic approach to senile cataracts: possible links with milk consumption, lactase activity, and galactose metabolism.
Does milk have a cataractogenic effect? Weighing of clinical evidence.
First reported case of lysinuric protein intolerance (LPI) in Lithuania, confirmed biochemically and by DNA analysis.
Idiopathic presenile and senile cataract formation and changes in lactase activity.
Lack of relationship between lactose absorption and senile cataracts.
Nutrition of orphan marsupials.
Synergistic effect of high lactase activity genotype and galactose-1-phosphate uridyl transferase (GALT) mutations on idiopathic presenile cataract formation.
Celiac Disease
A biopsy-based quick test in the diagnosis of duodenal hypolactasia in upper gastrointestinal endoscopy.
Association between celiac disease and primary lactase deficiency.
Celiac sprue among US military veterans: associated disorders and clinical manifestations.
Digestive and nutritional considerations in celiac disease: could supplementation help?
Extent of lactose absorption in children with active celiac disease.
Flow-cytometric detection of lactase expression in normal and coeliac intestinal epithelium.
High prevalence of celiac disease in patients with lactose intolerance.
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
Lactase enzyme, detected immunohistochemically, is lost in active celiac disease, but unaffected by oats challenge.
LACTOSURIA AND LACTASE DEFICIENCY IN ADULT CELIAC DISEASE.
Molecular and cellular aspects and regulation of intestinal lactase-phlorizin hydrolase.
Morphometric study of the jejunal mucosa in various childhood enteropathies with special reference to intraepithelial lymphocytes.
Selected disorders of malabsorption.
Sugar absorption by small bowel biopsy samples from patients with primary lactase deficiency and with adult celiac disease.
The clinical significance of disaccharide maldigestion.
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
[Carbohydrase activities may serve as a marker for small intestinal mucosal recovery in patients with celiac disease].
[Disorders of humoral regulation of the digestive organ functions in children with malabsorption syndromes]
[Intestinal microbiocenosis in children with intestinal enzymopathy]
[New cases of celiac disease detected by anti-endomysial antibody test in families of gluten-sensitive patients and among children examined for non-specific gastrointestinal complaints]
[The medical management of malabsorption (author's transl)]
Cholestasis
Lactose malabsorption is a risk factor for decreased bone mineral density in pancreatic insufficient cystic fibrosis patients.
Colic
Clinical Efficacy Of Lactase Enzyme Supplement In Infant Colic: A Randomised Controlled Trial.
Effect of lactase on infantile colic.
Efficacy and safety of APT198K for the treatment of infantile colic: a pilot study.
Improvement of symptoms in infant colic following reduction of lactose load with lactase.
Infant formula.
Infantile colic and feeding.
Infantile Colic: An Update.
Infantile colic: Is there a role for dietary interventions?
Colitis
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Morphological and biochemical alterations in the jejunum following iodoacetamide-induced colitis in rats.
[Disorders of lactase hydrolysis in patients with ulcerous colitis and irritable colon]
[New cases of celiac disease detected by anti-endomysial antibody test in families of gluten-sensitive patients and among children examined for non-specific gastrointestinal complaints]
[The use of parietal pH-metry in the diagnosis of intestinal diseases]
Colitis, Lymphocytic
Association of lymphocytic colitis and lactase deficiency in pediatric population.
Colitis, Ulcerative
A randomized multicenter clinical trial to evaluate the efficacy of melatonin in the prophylaxis of SARS-CoV-2 infection in high-risk contacts (MeCOVID Trial): A structured summary of a study protocol for a randomised controlled trial.
Incidence of lactase deficiency in ulcerative colitis.
INTESTINAL LACTASE DEFICIENCY IN ULCERATIVE COLITIS AND REGIONAL ILEITIS.
Lactase deficiency in ulcerative colitis, regional enteritis, and viral hepatitis.
Significance of lactase deficit in ulcerative colitis.
Simultaneous assessment of intestinal permeability and lactose tolerance with orally administered raffinose, lactose and L-arabinose.
[The use of parietal pH-metry in the diagnosis of intestinal diseases]
Colonic Neoplasms
Activity of the rat lactase gene promoter in transfected human colon cancer cells.
Diarrhea.
Effects of acetaldehyde on brush border enzyme activities in human colon adenocarcinoma cell line Caco-2.
Genotyping of the lactase-phlorizin hydrolase c/t-13910 polymorphism by means of a new rapid denaturing high-performance liquid chromatography-based assay in healthy subjects and colorectal cancer patients.
Immunohistological evidence, obtained with monoclonal antibodies, of small intestinal brush border hydrolases in human colon cancers and foetal colons.
Increased cell surface EGF receptor expression during the butyrate-induced differentiation of human HCT-116 colon tumor cell clones.
Lactase and sucrase-isomaltase gene expression during Caco-2 cell differentiation.
Potentiation of butyrate-induced differentiation in human colon tumor cells by deoxycholate.
RNA-Binding Protein Quaking, a Critical Regulator of Colon Epithelial Differentiation and a Suppressor of Colon Cancer.
Colorectal Neoplasms
Effect of growth and sodium butyrate on brush border membrane-associated hydrolases in human colorectal cancer cell lines.
Effects of the lactase 13910 C/T and calcium-sensor receptor A986S G/T gene polymorphisms on the incidence and recurrence of colorectal cancer in Hungarian population.
Evaluation of relationships among national colorectal cancer mortality rates, genetic lactase non-persistence status, and per capita yearly milk and milk product consumption.
Genotyping of the lactase-phlorizin hydrolase c/t-13910 polymorphism by means of a new rapid denaturing high-performance liquid chromatography-based assay in healthy subjects and colorectal cancer patients.
Intestinal brush-border-associated enzymes: co-ordinated expression in colorectal cancer.
The C/C-13910 genotype of adult-type hypolactasia is associated with an increased risk of colorectal cancer in the Finnish population.
[Lactose intolerance: past and present. Part II].
Common Variable Immunodeficiency
Primary acquired lactase deficiency with acquired hypogammaglobulinemia. Report of a case and review of the literature.
Congenital Abnormalities
Evolution of Lactase Persistence: Turbo-Charging Adaptation in Growth Under the Selective Pressure of Maternal Mortality?
Maternal Lactase Polymorphism (rs4988235) Is Associated with Neural Tube Defects in Offspring in the National Birth Defects Prevention Study.
Coronary Artery Disease
Association of the Lactase Persistence Haplotype Block With Disease Risk in Populations of European Descent.
COVID-19
Lactate dehydrogenase and susceptibility to deterioration of mild COVID-19 patients: a multicenter nested case-control study.
Crohn Disease
A randomized multicenter clinical trial to evaluate the efficacy of melatonin in the prophylaxis of SARS-CoV-2 infection in high-risk contacts (MeCOVID Trial): A structured summary of a study protocol for a randomised controlled trial.
Dairy sensitivity, lactose malabsorption, and elimination diets in inflammatory bowel disease.
Genetic adult lactase persistence is associated with risk of Crohn's Disease in a New Zealand population.
Hypolactasia and Crohn's disease: a myth.
INTESTINAL LACTASE DEFICIENCY IN ULCERATIVE COLITIS AND REGIONAL ILEITIS.
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
Lactase deficiency in ulcerative colitis, regional enteritis, and viral hepatitis.
Lactase deficiency: not more common in pediatric patients with inflammatory bowel disease than in patients with chronic abdominal pain.
Lactose intolerance in active Crohn's disease: clinical value of duodenal lactase analysis.
Molecular and cellular aspects and regulation of intestinal lactase-phlorizin hydrolase.
Regulation of sucrase-isomaltase gene expression in human intestinal epithelial cells by inflammatory cytokines.
Selective lactase deficiency is common in pediatric patients undergoing upper endoscopy.
[Breath-analysis tests in gastroenetrological diagnosis]
[New cases of celiac disease detected by anti-endomysial antibody test in families of gluten-sensitive patients and among children examined for non-specific gastrointestinal complaints]
Cryptosporidiosis
Oral bovine serum concentrate improves cryptosporidial enteritis in calves.
Cystic Fibrosis
An evolutionary approach to the high frequency of the Delta F508 CFTR mutation in European populations.
Cystic fibrosis and lactase persistence: a possible correlation.
Elevated meconium lactase activity. Its use as a screening test for cystic fibrosis.
INTESTINAL LACTASE DEFICIENCY IN A PATIENT WITH CYSTIC FIBROSIS. REPORT OF A CASE WITH ENZYME ASSAY.
Lactase deficiency in patients with cystic fibrosis.
Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis.
Newborn screening strategy for cystic fibrosis: a field study in an area with high allelic heterogeneity.
Selected disorders of malabsorption.
Small intestinal brush border enzymes in cystic fibrosis.
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
[Clinical effectiveness of the therapeutic nutrition of sick children using enteral feeding preparations and low-lactose mixtures]
[Lactase deficiency in children with cystic fibrosis of the pancreas (CFP)]
[Semiquantitative immunologic albumin demonstration and demonstration of lactase activity in meconium screening for cystic fibrosis]
[The predictive value of antigliadin antibodies (AGA) in the diagnosis of non-celiac gastrointestinal disease in children]
Cytomegalovirus Infections
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Dementia
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Dermatitis Herpetiformis
Celiac sprue among US military veterans: associated disorders and clinical manifestations.
Morphometric study of the jejunal mucosa in various childhood enteropathies with special reference to intraepithelial lymphocytes.
Dermatitis, Atopic
An adult with atopic dermatitis and repeated short-term fasting.
Diagnostic algorithm and peculiarities of monitoring for infants with disorders of the gastrointestinal tract.
Dermatitis, Contact
Lactase-induced occupational protein contact dermatitis and allergic rhinoconjunctivitis.
Diabetes Mellitus
Effects of diabetes and hyperglycemia on disaccharidase activities in the rat.
Evolutionary triangulation: informing genetic association studies with evolutionary evidence.
High prevalence of lactose absorbers in Northern Sardinian patients with type 1 and type 2 diabetes mellitus.
Lactose malabsorption is a risk factor for decreased bone mineral density in pancreatic insufficient cystic fibrosis patients.
Polysaccharide from Gynura divaricata modulates the activities of intestinal disaccharidases in streptozotocin-induced diabetic rats.
The lactase rs4988235 is associated with obesity related variables and diabetes mellitus in menopausal obese females.
Diabetes Mellitus, Type 1
High prevalence of lactose absorbers in Northern Sardinian patients with type 1 and type 2 diabetes mellitus.
Diabetes Mellitus, Type 2
Evolutionary triangulation: informing genetic association studies with evolutionary evidence.
High prevalence of lactose absorbers in Northern Sardinian patients with type 1 and type 2 diabetes mellitus.
Milk intake is not associated with low risk of diabetes or overweight-obesity: a Mendelian randomization study in 97,811 Danish individuals.
Down Syndrome
Genetic counseling and parental self-concept change.
Duodenal Diseases
Activity of duodenal disaccharidases in relation to normal and abnormal mucosal morphology.
Duodenal Ulcer
Study of enzyme activities in the descending part of the duodenum in patients of duodenal ulcer.
[Intestinal lactase and milk consumption before and after gastrectomy]
Duodenitis
Low activities of disaccharidases associated with inflamed duodenal bulb mucosa.
Dyspnea
Anaphylaxis to supplemental oral lactase enzyme.
Lactate dehydrogenase and susceptibility to deterioration of mild COVID-19 patients: a multicenter nested case-control study.
Eczema
Congenital lymphangiectasia and atopy.
Enteritis
Intestinal disaccharidases in malnourished infant rats.
Intestinal permeability and lactose hydrolysis in human rotaviral gastroenteritis assessed simultaneously by non-invasive differential sugar permeation.
Is lactase the receptor and uncoating enzyme for infantile enteritis (rota) viruses?
Molecular and cellular aspects and regulation of intestinal lactase-phlorizin hydrolase.
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
[Intestinal lactase deficiency in chronic enteritis and changes of its activity due to the therapy]
Enterocolitis
Association of Clostridium difficile with enterocolitis and lactose intolerance in a foal.
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Esophagitis
Gastrointestinal Conditions in Children With Severe Feeding Difficulties.
Exocrine Pancreatic Insufficiency
Digestive and nutritional considerations in celiac disease: could supplementation help?
Effect of pancreatic insufficiency and intestinal lactase deficiency on the gastric emptying of starch and lactose.
Influence of exocrine and endocrine pancreatic function on intestinal brush border enaymatic activities.
Quantitative fecal carbohydrate excretion in premature infants.
[The medical management of malabsorption (author's transl)]
Fatty Liver
Hypolactasia is associated with insulin resistance in nonalcoholic steatohepatitis.
Fetal Growth Retardation
Effect of intrauterine growth retardation on the activities of fetal intestinal enzymes in rats.
Food Hypersensitivity
Colonic mucosal eosinophilia in children without inflammatory bowel disease.
Fructose Intolerance
[Malabsorption syndrome as a result of lactase deficiency in combination with fructose intolerance]
Galactosemias
Infant formula.
Lactose metabolism and time to pregnancy.
[Clinical effectiveness of the therapeutic nutrition of sick children using enteral feeding preparations and low-lactose mixtures]
Gastritis
Gastrointestinal Conditions in Children With Severe Feeding Difficulties.
Gastritis, Atrophic
Enzyme activities in human gastric mucosa in gastritis and resected stomachs.
Human adult-onset lactase decline: an update.
Gastroenteritis
Absence of a cAMP-mediated antiabsorptive effect in an undifferentiated jejunal epithelium.
Demonstration of a difference in expression of maximal lactase and sucrase activity along the villus in the adult rat jejunum.
Diagnostic algorithm and peculiarities of monitoring for infants with disorders of the gastrointestinal tract.
Effect of a lactase preparation on lactose content and osmolality of preterm and term infant formulas.
Lactose avoidance for young children with acute diarrhoea.
Molecular and cellular aspects and regulation of intestinal lactase-phlorizin hydrolase.
Probiotics and medical nutrition therapy.
Transmissible gastroenteritis in pigs: some observations on laboratory aids to diagnosis.
[Abuse of artificial sweetener as differential diagnosis of lactose intolerance]
Gastroesophageal Reflux
Brush border enzyme activities in relation to histological lesion in pediatric celiac disease.
What is behind dyspepsia?
[Abdominal pain syndrome recurring after 40 years: critical revision]
[The predictive value of antigliadin antibodies (AGA) in the diagnosis of non-celiac gastrointestinal disease in children]
Gastrointestinal Diseases
A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe.
Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene.
Clinical Utility of LCT Genotyping in Children with Suspected Functional Gastrointestinal Disorder.
Diagnostic algorithm and peculiarities of monitoring for infants with disorders of the gastrointestinal tract.
Digestive Enzyme Supplementation in Gastrointestinal Diseases.
Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD).
Histochemistry of the human duodenal mucosa with special reference to the gradient of activities of the brush border enzymes.
Molecular genetics of human lactase deficiencies.
Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency.
Studies of ultramicrostructure in relation to disaccharidase activity in the jejunal mucosa.
Two novel mutations in the lactase gene in a Japanese infant with congenital lactase deficiency.
[Gastrointestinal and hepatic diseases].
Gastroparesis
What is behind dyspepsia?
Gastroschisis
Enterocytic gene expression is altered in experimental gastroschisis.
Genetic Diseases, Inborn
Asian and Pacific Islander Americans: An Overview of Demographic Characteristics and Health Care Issues.
Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives.
Genetic counseling and parental self-concept change.
Giardiasis
Disaccharidase deficiencies in Mongolian gerbils (Meriones unguiculatus) protected against Giardia lamblia.
Effect of Giardia lamblia on duodenal disaccharidase levels in humans.
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
Morphometric study of the jejunal mucosa in various childhood enteropathies with special reference to intraepithelial lymphocytes.
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
glucan 1,4-alpha-glucosidase deficiency
Congenital maltase-glucoamylase deficiency associated with lactase and sucrase deficiencies.
Patients with functional bowel disorder have disaccharidase deficiency: A single-center study from Russia.
[Disaccharidase deficiency and functional bowel diseases].
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Primary lactase deficiency and past malarial endemicity in Sardinia.
Glucosephosphate Dehydrogenase Deficiency
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Heart Diseases
Milk intake is not associated with ischaemic heart disease in observational or Mendelian randomization analyses in 98,529 Danish adults.
Hemochromatosis
Neolithic and Bronze Age migration to Ireland and establishment of the insular Atlantic genome.
Hemophilia A
Variation of rs3754689 at lactase gene and inhibitors in admixed Brazilian patients with hemophilia A.
Hepatic Encephalopathy
In vitro and in vivo lactose and lactulose effects on colonic fermentation and portal-systemic encephalopathy parameters.
In Vitro and In Vivo Lactose and Lactulose Effects on Colonic Fermentation and Portal-systemic Encephalopathy Parameters.
Treatment of chronic portal-systemic encephalopathy with lactose in lactase-deficient patients.
Hepatitis
Lactase deficiency in ulcerative colitis, regional enteritis, and viral hepatitis.
Hepatitis B
A randomized multicenter clinical trial to evaluate the efficacy of melatonin in the prophylaxis of SARS-CoV-2 infection in high-risk contacts (MeCOVID Trial): A structured summary of a study protocol for a randomised controlled trial.
Asian and Pacific Islander Americans: An Overview of Demographic Characteristics and Health Care Issues.
Hepatitis B, Chronic
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
HIV Infections
The impact of HIV infection on lactose absorptive capacity.
Hypercalcemia
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
Hypercalcemia and nephrocalcinosis in patients with congenital lactase deficiency.
Hyperglycemia
Effects of diabetes and hyperglycemia on disaccharidase activities in the rat.
Hyperlipidemias
Inhibitory effects of estrogens on digestive enzymes, insulin deficiency, and pancreas toxicity in diabetic rats.
Probiotics and medical nutrition therapy.
Hyperparathyroidism
Relationships between lactase activity and calcium absorption. Lactose intolerance in hyperparathyroidism.
Hypersensitivity
A randomized multicenter clinical trial to evaluate the efficacy of melatonin in the prophylaxis of SARS-CoV-2 infection in high-risk contacts (MeCOVID Trial): A structured summary of a study protocol for a randomised controlled trial.
Allergy to supplemental lactase enzyme.
Anaphylaxis to supplemental oral lactase enzyme.
Bloating and distention in irritable bowel syndrome: the role of gas production and visceral sensation after lactose ingestion in a population with lactase deficiency.
Diagnostic algorithm and peculiarities of monitoring for infants with disorders of the gastrointestinal tract.
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Molecularly defined adult-type hypolactasia in school-aged children with a previous history of cow's milk allergy.
Morphometric study of the jejunal mucosa in various childhood enteropathies with special reference to intraepithelial lymphocytes.
Occupational sensitization to lactase in the dietary supplement industry.
Probiotics and medical nutrition therapy.
Hypertension
Dairy consumption, systolic blood pressure, and risk of hypertension: Mendelian randomization study.
Lactate dehydrogenase and susceptibility to deterioration of mild COVID-19 patients: a multicenter nested case-control study.
The lactase persistence genotype is a protective factor for the metabolic syndrome.
Hypertension, Portal
Activity of brush border membrane enzymes in proximal jejunum of portal hypertensive rats.
Hypervitaminosis A
Effect of hypervitaminosis A on intestinal digestive & absorptive functions in rat.
Hypothyroidism
[Activity of intestinal lactase in patients with hypothyroidism]
Ichthyosis
Genetic counseling and parental self-concept change.
Ileus
Autoimmune Hemolytic Anemia Triggered by Infection with Human Parvovirus B19 after Total Abdominal Colectomy for Ulcerative Colitis.
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Infections
Biochemical analysis of jejunal brush border membrane of golden hamster: pathogenic modulations due to ancylostomiasis.
Disaccharidase activity in male and female C57BL/6 mice infected with Giardia muris.
Disaccharidase activity in the small intestine of susceptible and resistant mice after primary and challenge infections with Giardia muris.
Disaccharidase deficiencies in Mongolian gerbils (Meriones unguiculatus) protected against Giardia lamblia.
Enteropathogenic Escherichia coli enteritis: evaluation of the gnotobiotic piglet as a model of human infection.
Fermentable fiber reduces recovery time and improves intestinal function in piglets following Salmonella typhimurium infection.
Gut lactase activity: decrease during Salmonella typhimurium infection in mice.
Impact of chronic protein-calorie malnutrition on small intestinal repair after acute viral enteritis: a study in gnotobiotic piglets.
Intestinal enzyme profiles in normal and rotavirus-infected mice.
Intestinal infection with Nematospiroides dubius selectively increases lactase expression by mouse jejunal enterocytes.
Lactase deficiency in patients with intestinal schistosomiasis.
Lactase persistence, NOD2 status and Mycobacterium avium subsp. paratuberculosis infection associations to Inflammatory Bowel Disease.
Possible lymphocyte effects on lactase expression by mouse jejunal enterocytes.
Probiotics and medical nutrition therapy.
Rotaviral infection and intestinal lactase level.
The significance of lowered jejunal disaccharidase levels.
[Abdominal pain syndrome recurring after 40 years: critical revision]
Inflammatory Bowel Diseases
Diarrhea.
Geographic associations between lactase phenotype, multiple sclerosis, and inflammatory bowel diseases; Does obesity trump geography?
Global associations of national economic wealth are more robust with inflammatory bowel diseases than with obesity.
Lactase deficiency: not more common in pediatric patients with inflammatory bowel disease than in patients with chronic abdominal pain.
Lactase persistence, NOD2 status and Mycobacterium avium subsp. paratuberculosis infection associations to Inflammatory Bowel Disease.
Lactose intolerance in patients with inflammatory bowel diseases and dietary management in prevention of osteoporosis.
Latitude, sunshine, and human lactase phenotype distributions may contribute to geographic patterns of modern disease: the inflammatory bowel disease model.
Probiotics and medical nutrition therapy.
Selective lactase deficiency is common in pediatric patients undergoing upper endoscopy.
Insulin Resistance
Genotype C/C 13910 of the Lactase Gene as a Risk Factor for the Formation of Insulin-Resistant Obesity in Children.
Hypolactasia is associated with insulin resistance in nonalcoholic steatohepatitis.
Treatment of lactase deficiency in children's obesity with genotype c/c 13910 of lactase gene.
Intestinal Diseases
Lactose malabsorption and intolerance: What should be the best clinical management?
[Study of lactase deficiency as a pathogenic factor in acute and chronic intestinal diseases]
[The predictive value of antigliadin antibodies (AGA) in the diagnosis of non-celiac gastrointestinal disease in children]
[The use of parietal pH-metry in the diagnosis of intestinal diseases]
Intestinal Pseudo-Obstruction
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Iron Deficiencies
Decreased sucrase and lactase activity in iron deficiency is accompanied by reduced gene expression and upregulation of the transcriptional repressor PDX-1.
Disaccharidase levels in normal epithelium of the small intestine of rats with iron-deficiency anemia.
Irritable Bowel Syndrome
Bloating and distention in irritable bowel syndrome: the role of gas production and visceral sensation after lactose ingestion in a population with lactase deficiency.
Colonic mucosal eosinophilia in children without inflammatory bowel disease.
Comparison of Lactase Variant MCM6 -13910 C>T Testing and Self-report of Dairy Sensitivity in Patients With Irritable Bowel Syndrome.
Diarrhea.
IBS or intolerance?
Irritable bowel syndrome. Role of lactase deficiency.
Lactase activity in irritable colon syndrome.
Lactase and placebo in the management of the irritable bowel syndrome: a double-blind, cross-over study.
Lactase deficiency--a comparative study of diagnostic methods.
Lactase persistence/non-persistence genetic variants in irritable bowel syndrome in an endemic area for lactose malabsorption.
Lactose malabsorption, irritable bowel syndrome and self-reported milk intolerance.
Letter: Lactase activities in the irritable colon syndrome.
Polymorphism in the oxytocin promoter region in patients with lactase non-persistence is not related to symptoms.
Prevalence and presentation of lactose intolerance and effects on dairy product intake in healthy subjects and patients with irritable bowel syndrome.
Prevalence of lactase deficiency in British adults.
Probiotics and medical nutrition therapy.
Response of patients with irritable bowel syndrome and lactase deficiency using unfermented acidophilus milk.
[Disorders of lactase hydrolysis in patients with ulcerous colitis and irritable colon]
[Lactase deficiency and irritable colon]
[Lactase deficiency and the irritable colon syndrome]
[Prospects of probiotic strains of bifidobacteria and enterococcus in treatment and prevention of diseases in gastroenterology].
[Small intestinal bacterial overgrowth as a cause of lactase deficiency].
[The predictive value of antigliadin antibodies (AGA) in the diagnosis of non-celiac gastrointestinal disease in children]
[The role of small bowel microflora in the development of secondary lactase deficiency and the possibilities of its treatment with probiotics].
Kwashiorkor
The clinical significance of disaccharide maldigestion.
lactase deficiency
'The tropics in our bathroom': chronic diarrhoea after return from the tropics.
13CO2 breath test using naturally 13C-enriched lactose for detection of lactase deficiency in patients with gastrointestinal symptoms.
A boy with severe infantile gastrogen lactose intolerance and acquired lactase deficiency.
A Comparison Between Lactose Breath Test and Quick Test on Duodenal Biopsies for Diagnosing Lactase Deficiency in Patients With Self-reported Lactose Intolerance.
A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe.
A prospective study of persistent diarrhoea.
A racial difference in incidence of lactase deficiency. A survey of milk intolerance and lactase deficiency in healthy adult males.
A randomized multicenter clinical trial to evaluate the efficacy of melatonin in the prophylaxis of SARS-CoV-2 infection in high-risk contacts (MeCOVID Trial): A structured summary of a study protocol for a randomised controlled trial.
A re-appraisal of lactose intolerance.
A second enzyme defect in acquired lactase deficiency: lack of small-intestinal phlorizin-hydrolase.
A toxicological review of lactose to support clinical administration by inhalation.
Absorption of nutrients in lactase deficiency.
Activity of duodenal disaccharidases in relation to normal and abnormal mucosal morphology.
Acute abdominal distension in lactase deficiency relieved by metoclopramide.
Additional Value of CH? Measurement in a Combined (13)C/H? Lactose Malabsorption Breath Test: A Retrospective Analysis.
Adult human milk intolerance and intestinal lactase deficiency. A review.
Adult lactase deficiency: genetic control or adaptive response?
Allergy to cow's milk in the first year of life and its prevention.
An acidophilic beta-galactosidase from Bispora sp. MEY-1 with high lactose hydrolytic activity under simulated gastric conditions.
Analytical Validation of a New Enzymatic and Automatable Method for d-Xylose Measurement in Human Urine Samples.
Anomeric discrimination and rapid analysis of underivatized lactose, maltose, and sucrose in vegetable matrices by U-HPLC-ESI-MS/MS using porous graphitic carbon.
Another way to treat lactase deficiency.
Asian and Pacific Islander Americans: An Overview of Demographic Characteristics and Health Care Issues.
Assessment of a radiographic method for diagnosis of intestinal lactase deficiency: a prospective study.
Assessment of Lactose-Free Diet on the Phalangeal Bone Mineral Status in Italian Adolescents Affected by Adult-Type Hypolactasia.
Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene.
Association between celiac disease and primary lactase deficiency.
Association of LCT-13910 C/T Polymorphism and Colorectal Cancer.
Association of lymphocytic colitis and lactase deficiency in pediatric population.
Asymptomatic giardiasis in children.
beta-Galactosidase from Aspergillus niger in adult lactose malabsorption: a double-blind crossover study.
Bloating and distention in irritable bowel syndrome: the role of gas production and visceral sensation after lactose ingestion in a population with lactase deficiency.
Breath H2 test for lactase deficiency.
Breath hydrogen excretion after lactose and whole milk ingestion. A prospective comparison in lactase deficiency.
Breath hydrogen test after oral lactose in postgastrectomy patients.
Breath hydrogen test and stools characteristics after ingestion of milk and yogurt in malnourished children with chronic diarrhoea and lactase deficiency.
Breath hydrogen test for detecting lactose malabsorption in infants and children. Prevalence of lactose malabsorption in Japanese children and adults.
Calcium absorption and acceptance of low-lactose milk among children with primary lactase deficiency.
Calcium absorption from milk in lactase-deficient subjects.
Calcium metabolism in children with lactase deficiency.
Carbohydrate malabsorption in acute diarrhea.
Celiac sprue among US military veterans: associated disorders and clinical manifestations.
Chemotherapy-induced lactose intolerance in adults.
Circadian rhythm of breath hydrogen in young women.
Clinical application of breath hydrogen measurements.
Clinical Characteristics of Disaccharidase Deficiencies Among Children Undergoing Upper Endoscopy.
Clinical importance of lactase deficiency.
Clinical picture of hypolactasia and lactose intolerance.
Clinical significance of enzymatic deficiencies in the gastrointestinal tract with particular reference to lactase deficiency.
Colonic mucosal eosinophilia in children without inflammatory bowel disease.
Colonic mucosal inflammatory cells in children and adolescents with lactase deficiency.
Concordance of genetic and breath tests for lactose intolerance in a tertiary referral centre.
Congenital and adult intestinal lactase deficiency.
Congenital lactase deficiency.
Congenital lactase deficiency. A clinical study on 16 patients.
Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives.
Congenital lactose intolerance is triggered by severe mutations on both alleles of the lactase gene.
Congenital lymphangiectasia and atopy.
Congenital maltase-glucoamylase deficiency associated with lactase and sucrase deficiencies.
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
Correlation between symptoms developed after the oral ingestion of 50 g lactose and results of hydrogen breath testing for lactose intolerance.
Correlation in the diagnosis of intestinal lactase deficiency between the radiological method and the lactose tolerance test.
Cow's milk allergy versus cow milk intolerance.
Cronkhite-Canada syndrome. A case report and analytical review of 23 other cases reported in Japan.
Defects of sugar absorption. Some observations on racial lactase deficiency.
Demographic and Clinical Correlates of Mucosal Disaccharidase Deficiencies in Children With Functional Dyspepsia.
Demonstration of "hetero-beta-galactosidase" "in situ".
Development, Validation, and Applicability of a Symptoms Questionnaire for Lactose Malabsorption Screening.
Diagnosing lactase deficiency in three breaths.
Diagnosis of genetic predisposition for lactose intolerance by high resolution melting analysis.
Diagnostic algorithm and peculiarities of monitoring for infants with disorders of the gastrointestinal tract.
Diarrhea.
Dietary manipulation of postprandial colonic lactose fermentation: II. Addition of exogenous, microbial beta-galactosidases at mealtime.
Dietary treatment of lactose intolerance in infants and children.
Differences between lactase deficient and non-lactase deficient women with spinal osteoporosis.
Disaccharidase activities in small intestinal mucosa in patients with cystic fibrosis.
Disaccharidase activities in small intestine of rotavirus-infected suckling mice: a histochemical study.
Disaccharidase activity in children undergoing esophagogastroduodenoscopy: A systematic review.
Disaccharidase activity in the small intestine: prevalence of lactase deficiency in 100 healthy subjects.
Disaccharide consumption and malabsorption in Canadian Indians.
Disaccharide digestion and maldigestion.
Disorders of carbohydrate absorption in clinical practice.
Disorders of intestinal secretion and absorption.
Does low lactose milk powder improve the nutritional intake and nutritional status of frail older Chinese people living in nursing homes?
Does milk have a cataractogenic effect? Weighing of clinical evidence.
Does primary lactase deficiency reduce bone mineral density in postmenopausal women? A systematic review and meta-analysis.
Editorial: Lactase deficiency.
Effect of a lactase preparation on lactose content and osmolality of preterm and term infant formulas.
Effect of feeding yogurt versus milk in children with persistent diarrhea.
Effect of jaundice phototherapy on intestinal mucosal bilirubin concentration and lactase activity in the congenitally jaundiced Gunn Rat.
Effect of lactase preparations in asymptomatic individuals with lactase deficiency--gastric digestion of lactose and breath hydrogen analysis.
Effect of pancreatic insufficiency and intestinal lactase deficiency on the gastric emptying of starch and lactose.
Effect of pancreatic proteases on intestinal lactase activity.
Effects of Bifidobacterium longum and Lactobacillus rhamnosus on Gut Microbiota in Patients with Lactose Intolerance and Persisting Functional Gastrointestinal Symptoms: A Randomised, Double-Blind, Cross-Over Study.
Effects of diets containing dried whey on the lactase activity of the small intestinal mucosa and the contents of the small intestine and cecum of the pig.
Effects of Prebiotic and Probiotic Supplementation on Lactase Deficiency and Lactose Intolerance: A Systematic Review of Controlled Trials.
Efficacy of addition of exogenous lactase to milk in adult lactase deficiency.
Electrical assessment of functional lactase activity in conscious man.
Elevated IgM in dietary migraine with lactase deficiency.
Enzyme replacement therapy for primary adult lactase deficiency. Effective reduction of lactose malabsorption and milk intolerance by direct addition of beta-galactosidase to milk at mealtime.
Etiology of lactase deficiency: another perspective.
Evaluation of a hand-held hydrogen monitor in the diagnosis of intestinal lactase deficiency.
Evolution and lactase deficiency.
Excellent agreement between genetic and hydrogen breath tests for lactase deficiency and the role of extended symptom assessment.
Experience with a radiological method of diagnosing lactase deficiency.
Expression of a functional cold active ?-galactosidase from Planococcus sp-L4 in Pichia pastoris.
Family studies of lactase deficiency in the American Indian.
Feeding lactose-intolerant children with a powdered fermented milk.
First reported case of lysinuric protein intolerance (LPI) in Lithuania, confirmed biochemically and by DNA analysis.
Food hypersensitivity allergy or malabsorption.
Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD).
Frequency of lactose malabsorption among healthy southern and northern Indian populations by genetic analysis and lactose hydrogen breath and tolerance tests.
Frequency of LCT-13910C/T and LCT-22018G/A single nucleotide polymorphisms associated with adult-type hypolactasia/lactase persistence among Israelis of different ethnic groups.
From Treating Childhood Malnutrition to Public Health Nutrition.
Gastric emptying of maltose, sucrose, lactose and lactulose in rats with ontogenic lactase deficiency.
Gastrointestinal Conditions in Children With Severe Feeding Difficulties.
Gastrointestinal infections in Singapore children.
Genetic counseling and parental self-concept change.
Genetic predisposition for adult lactose intolerance and relation to diet, bone density, and bone fractures.
Genetic variation and lactose intolerance: detection methods and clinical implications.
Genetics of primary adult lactase deficiency.
Georges Brohee Prize 1988-1989. Assimilation of nutritional carbohydrates: influence of hydrolysis.
Giardiasis in childhood: poor clinical and histological correlations.
GRAND ROUNDS AT WASHINGTON UNIVERSITY SCHOOL OF MEDICINE. II. LACTASE DEFICIENCY IN THE SMALL INTESTINE OF AN ADULT.
Headaches and lactase deficiency.
High prevalence of celiac disease in patients with lactose intolerance.
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Human health effects of lactose consumption as food and drug ingredient.
Hydrogen excretion in pediatric lactose malabsorbers: relation to symptoms and the dose of lactose.
Hypercalcemia and nephrocalcinosis in patients with congenital lactase deficiency.
Hypolactasia and Crohn's disease: a myth.
Immunocytochemical heterogeneity of lactase-phlorizin hydrolase in adult lactase deficiency.
Immunohistochemical localization of intestinal glycosidases.
Impaired Trafficking and Subcellular Localization of a Mutant Lactase Associated With Congenital Lactase Deficiency.
In vitro and in vivo lactose and lactulose effects on colonic fermentation and portal-systemic encephalopathy parameters.
In Vitro and In Vivo Lactose and Lactulose Effects on Colonic Fermentation and Portal-systemic Encephalopathy Parameters.
Incidence and clinical significance of lactose malabsorption in adult coeliac disease.
Incidence of lactase deficiency in control subjects from India. Role of hereditary factors.
Incidence of lactase deficiency in ulcerative colitis.
Increased serum osteocalcin levels in patients with lactase deficiency.
Infant formula.
INFLUENCE OF CARBOHYDRATE MALABSORPTION SYNDROME ON THE CLINICAL COURSE OF ROTAVIRUS INFECTION IN CHILDREN AT AN EARLY AGE.
Intestinal absorption of calcium from yogurt in lactase-deficient subjects.
Intestinal beta-galactosidases in adult low lactase activity and in congenital lactase deficiency.
Intestinal beta-galactosidases. II. Biochemical alteration in human lactase deficiency.
Intestinal disaccharidase activity in patients with autism: Effect of age, gender, and intestinal inflammation.
Intestinal exfoliated cells in infant diarrhoea: changes in cell renewal and disaccharidase activities.
Intestinal lactase deficiency among east Indians. An adaptive rather than a genetically inherited phenomenon?
INTESTINAL LACTASE DEFICIENCY AND DIARRHEA IN ADULTS.
Intestinal lactase deficiency and lactose intolerance in adults.
Intestinal lactase deficiency and lactose intolerance in adults. Preliminary report.
INTESTINAL LACTASE DEFICIENCY AND LACTOSE INTOLERANCE IN ADULTS. PRELIMINARY REPORT.
Intestinal lactase deficiency and milk drinking capacity in the adult.
Intestinal lactase deficiency and milk drinking habits.
Intestinal lactase deficiency and saccharide malabsorption during oral neomycin administration.
INTESTINAL LACTASE DEFICIENCY IN A PATIENT WITH CYSTIC FIBROSIS. REPORT OF A CASE WITH ENZYME ASSAY.
Intestinal lactase deficiency in adult nonhuman primates: implications for selection pressures in man.
Intestinal lactase deficiency in an apparently normal Peruvian population.
Intestinal lactase deficiency in Ceylon (Sri Lanka).
Intestinal lactase deficiency in newborns with cystic fibrosis--dietary consequences.
INTESTINAL LACTASE DEFICIENCY IN ULCERATIVE COLITIS AND REGIONAL ILEITIS.
Intestinal lactase deficiency.
Intestinal lactase deficiency. Diagnosis by routine upper gastrointestinal radiography.
Intestinal Microbiota in Hirschsprung Disease.
Intestinal permeability and lactose hydrolysis in human rotaviral gastroenteritis assessed simultaneously by non-invasive differential sugar permeation.
Intestinal pH and propulsion: an explanation of diarrhoea in lactase deficiency and laxation by lactulose.
Irritable bowel syndrome. Role of lactase deficiency.
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
ISOLATED INTESTINAL LACTASE DEFICIENCY IN THE ADULT.
Isolated lactase deficiency in humans: report on 100 patients.
Isolated lactase deficiency producing postgastrectomy milk intolerance.
Jejunal disaccharidases and some observations on the cause of lactase deficiency.
Jejunal hetero-beta-galactosidase activities in Ugandans with lactase deficiency.
Laboratory evaluation of malassimilation in horses.
Lack of protection from rotavirus infection in children with congenital intestinal lactase deficiency.
Lactase deficiency a realistic approach.
Lactase deficiency among Malaysian children with recurrent abdominal pain.
Lactase deficiency and a lactose-free diet in patients with "unspecific abdominal complaints".
Lactase deficiency and lactose intolerance in a multiracial Asian population in Malaysia.
Lactase deficiency and lactose malabsorption.
Lactase deficiency and lactose malabsorption. A review.
Lactase deficiency and yogurt.
Lactase deficiency in a rural area of Mexico.
LACTASE DEFICIENCY IN ADULTS. A CAUSE OF "FUNCTIONAL" DIARRHOEA.
Lactase deficiency in Australian school children.
Lactase deficiency in de Toni-Debré-Fanconi Syndrome. Relationship between lactase activity and calcium absorption.
Lactase deficiency in Indians.
Lactase deficiency in Jewish communities in Israel.
Lactase deficiency in Mexican-American males.
Lactase deficiency in Nigerians.
Lactase deficiency in Orientals.
Lactase deficiency in osteoporosis.
Lactase deficiency in patients with cystic fibrosis.
Lactase deficiency in patients with intestinal schistosomiasis.
Lactase deficiency in patients with the "irritable-colon syndrome".
Lactase deficiency in Singapore-born and Canadian-born Chinese.
Lactase deficiency in Thailand.
Lactase deficiency in Thailand: effect of prolonged lactose feeding.
LACTASE DEFICIENCY IN THE ADULT. A COMMON OCCURRENCE.
Lactase deficiency in the South African black population.
Lactase deficiency in ulcerative colitis, regional enteritis, and viral hepatitis.
Lactase deficiency phenotype has not been selected by malaria.
Lactase Deficiency, Geriatric and Ethnic Considerations.
Lactase deficiency--a comparative study of diagnostic methods.
Lactase deficiency.
Lactase deficiency. Diagnosis and management.
Lactase deficiency: a common genetic trait of the American Indian.
Lactase deficiency: a potential novel aetiological factor in chronic pruritus of unknown origin.
Lactase deficiency: helping patients cope.
Lactase deficiency: not more common in pediatric patients with inflammatory bowel disease than in patients with chronic abdominal pain.
Lactase deficiency: prevalence in osteoporosis.
Lactase deficiency: the world pattern today.
Lactose absorption in patients with glucose 6-phosphate dehydrogenase deficiency with and without favism.
Lactose and calcium absorption in postmenopausal osteoporosis.
Lactose feeding and lactase deficiency.
Lactose Intolerance and Bone Health: The Challenge of Ensuring Adequate Calcium Intake.
Lactose intolerance and gastrointestinal cow's milk allergy in infants and children - common misconceptions revisited.
Lactose intolerance and intestinal villi morphology in Thai people.
Lactose intolerance and lactase deficiency in children.
Lactose intolerance and osteoporosis in men.
Lactose Intolerance and Other Disaccharidase Deficiency.
Lactose intolerance and self-reported milk intolerance: relationship with lactose maldigestion and nutrient intake. Lactase Deficiency Study Group.
Lactose intolerance and the irritable colon.
Lactose intolerance genetic testing: is it useful as routine screening? Results on 1426 south-central Italy patients.
Lactose intolerance in a calf.
Lactose intolerance in adults with chronic unspecific abdominal complaints.
Lactose Intolerance in Adults: Biological Mechanism and Dietary Management.
Lactose intolerance in East Indians of Trinidad.
Lactose intolerance in infants, children, and adolescents.
Lactose intolerance.
Lactose intolerance: a non-allergic disorder often managed by allergologists.
Lactose intolerance: diagnosis and management.
Lactose intolerance: problems in diagnosis and treatment.
Lactose malabsorption and intolerance: What should be the best clinical management?
Lactose malabsorption from yogurt, pasteurized yogurt, sweet acidophilus milk, and cultured milk in lactase-deficient individuals.
Lactose malabsorption in Greek adults: correlation of small bowel transit time with the severity of lactose intolerance.
Lactose malabsorption in the elderly: role of small intestinal bacterial overgrowth.
Lactose malabsorption is not a cause of diarrhea during phototherapy.
Lactose malabsorption, irritable bowel syndrome and self-reported milk intolerance.
Lactose malabsorption.
LACTOSE TOLERANCE AND RISK OF MULTIFACTORIAL DISEASES ON THE EXAMPLE OF GASTROINTESTINAL TRACT AND BONE TISSUEPATHOLOGIES.
Lactose-barium study as a screening test for lactase deficiency.
Lactose-intolerance may induce severe chronic eczema.
Lactose-poor milk in adult lactose intolerance.
LACTOSURIA AND LACTASE DEFICIENCY IN ADULT CELIAC DISEASE.
Lactosuria in the African with lactase deficiency.
Letter: H2 breath test for lactase deficiency.
Letter: Intestinal lactase deficiency as a factor in the diarrhea of light-treated jaundiced infants.
Low prevalence of lactase persistence in Neolithic South-West Europe.
Low-dose lactose in drugs neither increases breath hydrogen excretion nor causes gastrointestinal symptoms.
Lowering the milk lactose content in vivo: potential interests, strategies and physiological consequences.
Management and treatment of lactose malabsorption.
Maternal Lactase Polymorphism (rs4988235) Is Associated with Neural Tube Defects in Offspring in the National Birth Defects Prevention Study.
Measurement of 14C-lactose absorption in the diagnosis of lactase deficiency.
Mechanisms in adverse reactions to food. The gastrointestinal tract.
Metabolic bone disease as a result of lactase deficiency.
Milk intolerance and microbe-containing dairy foods.
Milk intolerance following gastric operations with special reference to lactase deficiency.
Milk protein-free diet for nonseasonal asthma and migraine in lactase-deficient patients.
Molecular and cellular aspects and regulation of intestinal lactase-phlorizin hydrolase.
Molecular differentiation of congenital lactase deficiency from adult-type hypolactasia.
Molecular genetics of human lactase deficiencies.
Morphometric study of the jejunal mucosa in various childhood enteropathies with special reference to intraepithelial lymphocytes.
Mucosal abnormalities in microsporidiosis.
Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency.
No evidence for an effect of lactase deficiency on bone mass in pre- or postmenopausal women.
No evidence of lactase deficiency related to phototherapy of jaundiced infants.
Nutrition in prevention of osteoporosis.
Nutritional management of lactose intolerance: the importance of diet and food labelling.
Origins and implications of the distribution of adult lactase deficiency in human populations.
Osteoporosis and primary intestinal lactase deficiency.
Osteoporosis, intestinal lactase deficiency and low dietary calcium intake.
Patients with functional bowel disorder have disaccharidase deficiency: A single-center study from Russia.
Peroral gene therapy of lactose intolerance using an adeno-associated virus vector.
Post-gastrectomy steatorrhoea due to intestinal lactase deficiency.
Prevalence and presentation of lactose intolerance and effects on dairy product intake in healthy subjects and patients with irritable bowel syndrome.
Prevalence of Disaccharidase Deficiency in Adults With Unexplained Gastrointestinal Symptoms.
Prevalence of lactase deficiency in British adults.
Prevalence of primary lactase deficiency in adult residents of west Birmingham.
Prevention and management of osteoporosis: consensus statements from the Scientific Advisory Board of the Osteoporosis Society of Canada. 4. Calcium nutrition and osteoporosis.
Primary acquired lactase deficiency with acquired hypogammaglobulinemia. Report of a case and review of the literature.
Primary intestinal lactase deficiency.
Primary lactase deficiency and bone mineral density in postmenopausal women.
Primary lactase deficiency and past malarial endemicity in Sardinia.
Primary lactase deficiency in Greek adults.
Primary lactase deficiency: genetic or acquired?
Prospective comparison of indirect methods for detecting lactase deficiency.
Protein patterns of brush-border fragments in congenital lactose malabsorption and in specific hypolactasia of the adult.
Protein-losing enteropathy following the Fontan procedure in a child with intestinal lactase deficiency treated with lactose-free diet.
Quantitative fecal carbohydrate excretion in premature infants.
Recessive inheritance of the adult type of intestinal lactase deficiency.
Recurrent abdominal pain and lactose absorption in children.
Reference Intervals for Intestinal Disaccharidase Activities Determined from a Non-Reference Population.
Relationships between disaccharidase deficiencies, duodenal inflammation and symptom profile in children with abdominal pain.
Release of ?-galactosidase from poloxamine/?-cyclodextrin hydrogels.
Response of patients with irritable bowel syndrome and lactase deficiency using unfermented acidophilus milk.
Role of gastric emptying in functional dyspepsia: a scintigraphic study of 94 subjects.
Selected disorders of malabsorption.
Selective alteration of brush-border hydrolases in intestinal diseases in childhood.
Selective lactase deficiency is common in pediatric patients undergoing upper endoscopy.
Separation and characterization of four enzyme forms of beta-galactosidase from Saccharomyces lactis.
Serum lipids and proteins in lactose malabsorption.
Simultaneous assessment of intestinal permeability and lactose tolerance with orally administered raffinose, lactose and L-arabinose.
Small intestinal function in chronic relapsing pancreatitis.
Small intestinal lactase status, frequency distribution of enzyme activity and milk intake in a multi-ethnic population.
Soy infant formula: is it that bad?
Specific small-intestinal lactase deficiency in adults.
Structural determinants for transport of lactase phlorizin-hydrolase in the early secretory pathway as a multi-domain membrane glycoprotein.
Studies of ultramicrostructure in relation to disaccharidase activity in the jejunal mucosa.
Studies on small intestinal mucosal morphology lactase activity and lactose hydrolysis rate in childhood with diarrhea.
Sucrase-Isomaltase Deficiency as a Potential Masquerader in Irritable Bowel Syndrome.
Sucrase-Isomaltase Gene Variants in Patients with Abnormal Sucrase Activity and Functional GI Disorders.
Sugar absorption by small bowel biopsy samples from patients with primary lactase deficiency and with adult celiac disease.
Temproary intestinal lactase deficiency in light-treated jaundiced infants.
The acceptability of milk and milk products in populations with a high prevalence of lactose intolerance.
The activity of three different small-intestinal -galactosidases in adults with and without lactase deficiency.
The basic aspects of the chemical background of lactase deficiency.
The biosynthetic basis of adult lactase deficiency.
The clinical significance of lactose intolerance.
The diagnosis and management of patients with lactose-intolerance.
The effect of phototherapy on intestinal mucosal enzyme activity in the Gunn rat.
The effectiveness of 50% lactose-reduced milk in alleviating milk intolerance.
The enzymology of intestinal disease.
The geographical incidence of lactase deficiency.
The geography of chronic digestive disease in southern Africa.
The impact of HIV infection on lactose absorptive capacity.
The incidence of lactase deficiency following partial gastrectomy.
The noninvasive biochemical diagnosis of gastrointestinal disease, with special reference to children.
The prevalence of lactase deficiency and lactose intolerance in Chinese children of different ages.
The Roentgenologic Diagnosis Of Lactase Deficiency.
The role of calcium in human aging.
The role of milk and lactose intolerance in Ethiopian patients with non-ulcer dyspepsia: a case control study.
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
The threshold levels of milk consumption in individuals with lactase deficiency.
Thyrotoxicosis in a neonate of a mother with no history of thyroid disease.
Tolerance to lactose among lactase-deficient American Indians.
Treatment efficacy of a low FODMAP diet compared to a low lactose diet in IBS patients: A randomized, cross-over designed study.
Treatment of chronic portal-systemic encephalopathy with lactose in lactase-deficient patients.
Treatment of lactase deficiency in children's obesity with genotype c/c 13910 of lactase gene.
Trehalase deficiency in Greenland.
Tribal incidence of lactase deficiency in Uganda.
Two novel mutations in the lactase gene in a Japanese infant with congenital lactase deficiency.
Undernourished Children and Milk Lactose.
Update on lactose malabsorption and intolerance: pathogenesis, diagnosis and clinical management.
Use of a Novel Probiotic Formulation to Alleviate Lactose Intolerance Symptoms-a Pilot Study.
Use of genetic testing for hypolactasia trait in the North Denmark Region.
Use of lactose-hydrolyzed human milk in congenital lactase deficiency.
Use of oral sodium cromoglycate in persistent diarrhoea.
Use of the lactose-ethanol tolerance test in diabetes.
What is behind dyspepsia?
[14CO2 exhalation tests. Diagnostic improvement in gastroenterologic diseases]
[57-year-old female patient in early retirement with underweight and chronic-relapsing diarrhoea]
[Abuse of artificial sweetener as differential diagnosis of lactose intolerance]
[Analysis of lactase activities of small intestine mucous membrane by double labeled stable isotope technique in subjects with lactase deficiency]
[Breath hydrogen for detecting lactase deficiency. I. Methodological and statistical analysis (author's transl)]
[Breath hydrogen for detecting lactase deficiency. II. Relation between intestinal lactase activity, breath hydrogen and blood glucose during lactose tolerance test in 73 adult patients (author's transl)]
[Breath-analysis tests in gastroenetrological diagnosis]
[Comparative study of the gastric emptying of disaccharides and their respective monosaccharides in rats with ontogenic lactase deficiency]
[Comparative study of the primary lactase deficiency in two different adult populations (55 inhabitants of Nice and 55 Maghrebins) (author's transl)]
[Congenital lactase deficiency--a more common disease than previously thought?]
[Congenital lactase deficiency: Identification of a new mutation.]
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
[Current problems of lactase deficiency]
[Determination of lactase deficiency by the hydrogen breath test: a study of 198 healthy Chinese subjects]
[Determination of lactose intolerance frequency in children with food allergy]
[Diagnosis of intestinal lactase deficiency in children. Histochemical lactase determination in connection with results from the peroral lactose test and evaluation of intestinal mucosal structure]
[Diagnosis of lactase deficiency by exhaled air counting method using C14-lactose]
[Diagnosis of lactase deficiency with the expired hydrogen (H2) test]
[Diagnostics of lactose-malabsorption: value of tolerance tests and 14CO2 exhalation test in patients with and without lactase deficiency (author's transl)]
[Digestive parasitic diseases and lactase deficiency in children]
[Disaccharidase deficiency and functional bowel diseases].
[Disorders of humoral regulation of the digestive organ functions in children with malabsorption syndromes]
[Editorial: Lactase deficiency]
[Exhaled hydrogen test in the detection of lactase deficiency]
[Glucose tolerance test in the diagnosis of intestinal lactase deficiency]
[Gluten-sensitive enteropathy with intestinal T-cell lymphoma: an unusual cause of in disabling osteomalacia]
[Hydrogen breath tests in the diagnosis of primary lactase deficiency]
[Immunological aspects of food intolerance in children during first years of life]
[Incidence of lactase deficiency in patients with involution osteoporosis and in normal subjects. Its effect on the nutritional intake of calcium and phosphorus]
[Incidence of lactose intolerance in postmenopausal osteoporosis]
[Influence of the lactose free and lactose containing diet on prevalence of gram-negative sepsis and feeding intolerance in very low birth weight infants: double-blind randomized trial]
[Intestinal disaccharidase and alkaline phosphatase activities of jejunal biopsies in small bowel diseases of children (author's transl)]
[Intestinal lactase deficiency in chronic enteritis and changes of its activity due to the therapy]
[Intestinal microbiocenosis in children with intestinal enzymopathy]
[Jejunal mucosa in children with mucoviscidosis]
[Lactase deficiency (diarrhea caused by milk). 2]
[Lactase deficiency among representatives of various nationalities of Siberia]
[Lactase deficiency and irritable colon]
[Lactase deficiency and lactose intolerance-related symptoms in adult healthy subjects from western France]
[Lactase deficiency and the irritable colon syndrome]
[Lactase deficiency as cause of chronic recurrent diarrhea]
[Lactase deficiency in aboriginal inhabitants of the Mordovian and Karelian ASSR]
[Lactase deficiency in children of the first year of life]
[Lactase deficiency in children with cystic fibrosis of the pancreas (CFP)]
[Lactase deficiency in children with secondary milk intolerance]
[Lactase deficiency in patients with non-specific abdominal symptoms]
[Lactase deficiency in patients with postinfectious irritable bowel syndrome and the role of intestinal microflora in its development].
[Lactase deficiency in the intestinal mucosa. Demonstration by hydrogen detection in the expired air after lactose loading (author's transl)]
[Lactase deficiency syndrome]
[Lactase deficiency: incidence, mode of inheritance and practical implications]
[Lactase deficiency]
[Lactose digestion by milk fermented with Lactobacillus acidophilus and Lactobacillus casei of human origin]
[Lactose intolerance and lactase deficiency in adult patients in Curacao]
[Lactose intolerance caused by lactase deficiency]
[Lactose intolerance in neonates with non-infectious diarrhea].
[Lactose intolerance: pathophysiology, clinical symptoms, diagnosis and treatment]
[Lactose intolerance].
[Lactose tolerance in children with chronic gastroduodenal zone diseases]
[Lactulose fermentation and lactose absorption in Chilean patients with liver cirrhosis: importance for hepatic encephalopathy therapy]
[Late results od selective proximal vagotomy with or without pyloroplasty in uncomplicated chronic duodenal ulcer]
[Malabsorption of carbohydrates in children (author's transl)]
[Malabsorption syndrome as a result of lactase deficiency in combination with fructose intolerance]
[Milk intolerance, lactose intolerance and lactase deficiency in partial resection of the stomach]
[Morphology and histochemistry of the jejunal mucosa in patients with lactase deficiency]
[New cases of celiac disease detected by anti-endomysial antibody test in families of gluten-sensitive patients and among children examined for non-specific gastrointestinal complaints]
[Nutritional status and breath hydrogen test with lactose and lactulose in Terena Indian children]
[Partial trisomy 1q25-1q32 in a boy with isolated lactase deficiency]
[Poor digestion of lactose. Its definition, prevalence in Mexico, and its implications in milk consumption]
[Prevalence of the lactase deficiency among the population of the northwestern region of Russia]
[Primary lactose malabsorption in healthy Brazilian adult caucasoid, negroid and mongoloid subjects]
[Probiotic bacteria and lactase deficiencies]
[Progress on the research of lactose intolerance].
[Prospects of probiotic strains of bifidobacteria and enterococcus in treatment and prevention of diseases in gastroenterology].
[Radiological diagnosis of lactase deficiency]
[Secondary lactase deficiency and the milk intolerance syndrome in chronic digestive tract diseases]
[Secondary lactase deficiency in children and its epidemiologic implications]
[Small intestinal bacterial overgrowth as a cause of lactase deficiency].
[Study of lactase deficiency as a pathogenic factor in acute and chronic intestinal diseases]
[Study of the functional behavior of the enterochromaffin cell system after lactose loading in patients with intestinal lactase deficiency]
[Study on the incidence of lactose intolerance of children in China]
[The clinical pictures of rotavirus infection in childhood. Studies on the admissions to the Clinica Pediatrica di Catania in 1984-1988]
[The colon as an organ: habitat of bacterial flora]
[The hydrogen breath test in the diagnosis of primary lactase deficiency]
[The medical management of malabsorption (author's transl)]
[The predictive value of antigliadin antibodies (AGA) in the diagnosis of non-celiac gastrointestinal disease in children]
[The prevalence of lactase deficiency among the peoples of the USSR]
[The quantitative disaccharidase activity of the human small intestine and acquired lactase deficiency in adults]
[The role of small bowel microflora in the development of secondary lactase deficiency and the possibilities of its treatment with probiotics].
[Use of the association of radiological and glycemic findings compared with the determination of jejunal lactase for study of lactase deficiency]
[Useful and superfluous measures in the treatment of infant diarrhea]
[Useful genetic test for lactase deficiency]
Lactose Intolerance
13910C>T and 22018G>A LCT gene polymorphisms in diagnosing hypolactasia in children.
A biopsy-based quick test in the diagnosis of duodenal hypolactasia in upper gastrointestinal endoscopy.
A boy with severe infantile gastrogen lactose intolerance and acquired lactase deficiency.
A Comparison Between Lactose Breath Test and Quick Test on Duodenal Biopsies for Diagnosing Lactase Deficiency in Patients With Self-reported Lactose Intolerance.
A cross-sectional survey of sensitization to Aspergillus oryzae-derived lactase in pharmaceutical workers.
A Diagnostic Approach to Patients with Suspected Lactose Malabsorption.
A genetic test which can be used to diagnose adult-type hypolactasia in children.
A geographic approach to senile cataracts: possible links with milk consumption, lactase activity, and galactose metabolism.
A novel intestinal trans-factor (NF-LPH1) interacts with the lactase-phlorizin hydrolase promoter and co-varies with the enzymatic activity.
A re-appraisal of lactose intolerance.
A study of lactose absorption capacity in twins.
ACQUIRED MILK INTOLERANCE IN THE ADULT CAUSED BY LACTOSE MALABSORPTION DUE TO A SELECTIVE DEFICIENCY OF INTESTINAL LACTASE ACTIVITY.
Additional Value of CH? Measurement in a Combined (13)C/H? Lactose Malabsorption Breath Test: A Retrospective Analysis.
Adult lactose digestion status and effects on disease.
Adult lactose intolerance, calcium intake, bone metabolism and bone density in German-Turkish immigrants.
Adult-type hypolactasia and regulation of lactase expression.
All lactase preparations are not the same: results of a prospective, randomized, placebo-controlled trial.
Analysis of lactase in lactose intolerance supplements.
Analytical Validation of a New Enzymatic and Automatable Method for d-Xylose Measurement in Human Urine Samples.
Anaphylaxis to supplemental oral lactase enzyme.
Anomeric discrimination and rapid analysis of underivatized lactose, maltose, and sucrose in vegetable matrices by U-HPLC-ESI-MS/MS using porous graphitic carbon.
Application relevant studies of fungal beta-galactosidases with potential application in the alleviation of lactose intolerance.
Assessment of hypolactasia and site-specific intestinal permeability by differential sugar absorption of raffinose, lactose, sucrose and mannitol.
Assessment of Lactose-Free Diet on the Phalangeal Bone Mineral Status in Italian Adolescents Affected by Adult-Type Hypolactasia.
Association between celiac disease and primary lactase deficiency.
Association of Lactase Persistence Genotypes (rs4988235) and Ethnicity with Dairy Intake in a Healthy U.S. Population.
Beja and Nilotes: nomadic pastoralist groups in the Sudan with opposite distributions of the adult lactase phenotypes.
beta-Galactosidase from Aspergillus niger in adult lactose malabsorption: a double-blind crossover study.
Breath hydrogen as a diagnostic method for hypolactasia.
Breath hydrogen test after oral lactose in postgastrectomy patients.
Can primary hypolactasia manifest itself after the age of 20 years? A two-decade follow-up study.
Carbohydrate malabsorption syndromes and early signs of mental depression in females.
Characterization of crystalline forms of gaxilose, a diagnostic drug.
Clinical and nutritional implications of radiation enteritis.
Clinical aspects of lactose intolerance in children and adults.
Clinical picture of hypolactasia and lactose intolerance.
Clinical Utility of LCT Genotyping in Children with Suspected Functional Gastrointestinal Disorder.
Colonic fermentation may play a role in lactose intolerance in humans.
Comparison of indirect diagnostic methods for hypolactasia.
Comparison of Lactase Variant MCM6 -13910 C>T Testing and Self-report of Dairy Sensitivity in Patients With Irritable Bowel Syndrome.
Comparison of quick point of care test for small bowel hypolactasia with biochemical lactase assay in children.
Complete deficiency of brush-border lactase in congenital lactose malabsorption.
Congenital lactose intolerance is triggered by severe mutations on both alleles of the lactase gene.
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
Control of lactase in human adult-type hypolactasia and in weaning rabbits and rats.
Correlation of G/A -22018 single-nucleotide polymorphism with lactase activity and its usefulness in improving the diagnosis of adult-type hypolactasia among North Indian children.
Correlation of lactase activity, lactose tolerance and milk consumption in different age groups.
Country, regional, and global estimates for lactose malabsorption in adults: a systematic review and meta-analysis.
Dairy Foods: Are They Politically Correct?
Dairy sensitivity, lactose malabsorption, and elimination diets in inflammatory bowel disease.
Decline of lactase activity and c/t-13910 variant in Sardinian childhood.
Development of a new method for d-xylose detection and quantification in urine, based on the use of recombinant xylose dehydrogenase from Caulobacter crescentus.
Diagnosing lactase deficiency in three breaths.
Diagnosing lactose malabsorption in children: difficulties in interpreting hydrogen breath test results.
Diagnosis and clinical observation of lactose-free milk powder on treatment of neonatal diarrhea.
Dietary manipulation of postprandial colonic lactose fermentation: II. Addition of exogenous, microbial beta-galactosidases at mealtime.
Disaccharidase activities in children: normal values and comparison based on symptoms and histologic changes.
Distribution of the - 13910C>T polymorphism in the general population of Portugal and in subjects with gastrointestinal complaints associated with milk consumption.
Distribution of the lactase phenotypes in the population of the Democratic Republic of the Sudan.
Effect of a lactase preparation on lactose content and osmolality of preterm and term infant formulas.
Effect of a single dose of lactase on symptoms and expired hydrogen after lactose challenge in lactose-intolerant subjects.
Effect of C/T -13910 cis-acting regulatory variant on expression and activity of lactase in Indian children and its implication for early genetic screening of adult-type hypolactasia.
Effect of dietary lactose on the absorption of protein, fat and calcium in the postweaning rat.
Effect of lactase on symptoms and hydrogen breath levels in lactose intolerance: A crossover placebo-controlled study.
Effect of lactose on oro-cecal transit in lactose digesters and maldigesters.
Effects of Bifidobacterium longum and Lactobacillus rhamnosus on Gut Microbiota in Patients with Lactose Intolerance and Persisting Functional Gastrointestinal Symptoms: A Randomised, Double-Blind, Cross-Over Study.
Effects of diets containing dried whey on the lactase activity of the small intestinal mucosa and the contents of the small intestine and cecum of the pig.
Effects of exogenous lactase administration on hydrogen breath excretion and intestinal symptoms in patients presenting lactose malabsorption and intolerance.
Effects of malnutrition on expression and activity of lactase in children.
Effects of Prebiotic and Probiotic Supplementation on Lactase Deficiency and Lactose Intolerance: A Systematic Review of Controlled Trials.
Effects of the lactase 13910 C/T and calcium-sensor receptor A986S G/T gene polymorphisms on the incidence and recurrence of colorectal cancer in Hungarian population.
Efficacy of addition of exogenous lactase to milk in adult lactase deficiency.
Efficacy of exogenous lactase for lactose intolerance.
Electrical assessment of functional lactase activity in conscious man.
Enzymatic maturation of the gastrointestinal tract and its relevance to food allergy and intolerance in infancy.
Enzyme replacement therapy for primary adult lactase deficiency. Effective reduction of lactose malabsorption and milk intolerance by direct addition of beta-galactosidase to milk at mealtime.
Evaluation of a genetic test for diagnose of primary hypolactasia in northeast of iran (khorasan).
Evaluation of a new DNA test compared with the lactose hydrogen breath test for the diagnosis of lactase non-persistence.
Evaluation of breath, plasma, and urinary markers of lactose malabsorption to diagnose lactase non-persistence following lactose or milk ingestion.
Evaluation of differential disaccharide excretion in urine for non-invasive investigation of altered intestinal disaccharidase activity caused by alpha-glucosidase inhibition, primary hypolactasia, and coeliac disease.
Familial aquagenic urticaria associated with familial lactose intolerance.
Frequency of lactose malabsorption among healthy southern and northern Indian populations by genetic analysis and lactose hydrogen breath and tolerance tests.
Frequency of LCT -13910C>T single nucleotide polymorphism associated with adult-type hypolactasia/lactase persistence among Brazilians of different ethnic groups.
From 'lactose intolerance' to 'lactose nutrition'.
Genetic predisposition for adult lactose intolerance and relation to diet, bone density, and bone fractures.
Genetic testing for adult-type hypolactasia in Italian families.
Genetic testing improves the diagnosis of adult type hypolactasia in the Mediterranean population of Sardinia.
Genetic variant of lactase-persistent C/T-13910 is associated with bone fractures in very old age.
Genetic variation and lactose intolerance: detection methods and clinical implications.
Genetics and epidemiology of adult-type hypolactasia.
Genetics of lactase persistence and lactose intolerance.
Genotyping of the lactase-phlorizin hydrolase c/t-13910 polymorphism by means of a new rapid denaturing high-performance liquid chromatography-based assay in healthy subjects and colorectal cancer patients.
Giardiasis causing chronic diarrhoea in suburban Copenhagen: incidence, physical growth, clinical symptoms and small intestinal abnormality.
Hormone induced changes in lactase glycosylation in developing rat intestine.
Human health effects of lactose consumption as food and drug ingredient.
Hydrogen excretion in pediatric lactose malabsorbers: relation to symptoms and the dose of lactose.
Hypolactasia and lactase persistence. Historical review and the terminology.
Hypolactasia as a molecular basis of lactose intolerance.
Hypolactasia: a common enzyme deficiency leading to lactose malabsorption and intolerance.
Identification of a variant associated with adult-type hypolactasia.
Immunocytochemical heterogeneity of lactase-phlorizin hydrolase in adult lactase deficiency.
Immunoelectrophoretic studies on human small intestinal brush border proteins--amount of lactase protein in adult-type hypolactasia.
Impact of molecularly defined hypolactasia, self-perceived milk intolerance and milk consumption on bone mineral density in a population sample in Northern Europe.
Improvement of symptoms in infant colic following reduction of lactose load with lactase.
Improving diagnosis of adult-type hypolactasia in patients with abdominal complaints.
Influence of duodenal secretions and its components on release and activities of human brush-border enzymes.
Intestinal disaccharidase activities and activity ratios in a group of 60 adult German subjects.
Intestinal exfoliated cells in infant diarrhoea: changes in cell renewal and disaccharidase activities.
Intestinal lactase deficiency and lactose intolerance in adults.
Intestinal lactase deficiency and lactose intolerance in adults. Preliminary report.
INTESTINAL LACTASE DEFICIENCY AND LACTOSE INTOLERANCE IN ADULTS. PRELIMINARY REPORT.
Investigating thermal stability based on the structural changes of lactase enzyme by several orthogonal methods.
Lactase deficiency and lactose intolerance in a multiracial Asian population in Malaysia.
Lactase deficiency and lactose malabsorption.
Lactase deficiency and lactose malabsorption. A review.
Lactase deficiency in patients with intestinal schistosomiasis.
Lactase deficiency--a comparative study of diagnostic methods.
Lactase degradation by human enteric bacteria.
Lactase enzyme, detected immunohistochemically, is lost in active celiac disease, but unaffected by oats challenge.
Lactase genetic polymorphisms and coeliac disease in children: a cohort study.
Lactase insufficiency revisited.
Lactase Non-persistence and Lactose Intolerance.
Lactase non-persistence and milk consumption in Estonia.
Lactase Non-Persistence Genotyping: Comparison of Two Real-Time PCR Assays and Assessment of Concomitant Fructose/Sorbitol Malabsorption Rates.
Lactase non-persistent genotype distribution in Italy.
Lactase persistence genotypes and malaria susceptibility in Fulani of Mali.
Lactase persistence versus lactose intolerance: Is there an intermediate phenotype?
Lactase persistence/non-persistence genetic variants in irritable bowel syndrome in an endemic area for lactose malabsorption.
Lactase persistence/non-persistence variants, C/T_13910 and G/A_22018, as a diagnostic tool for lactose intolerance in IBS patients.
Lactase treated feeds to promote growth and feeding tolerance in preterm infants.
Lactic acid bacteria and the human gastrointestinal tract.
Lactose digestion by human jejunal biopsies: the relationship between hydrolysis and absorption.
Lactose induced redox-dependent senescence and activated Nrf2 pathway.
Lactose intolerance and lactase deficiency in children.
Lactose intolerance and self-reported milk intolerance: relationship with lactose maldigestion and nutrient intake. Lactase Deficiency Study Group.
Lactose intolerance and the genetic regulation of intestinal lactase-phlorizin hydrolase.
Lactose intolerance and the irritable colon.
Lactose intolerance in active Crohn's disease: clinical value of duodenal lactase analysis.
Lactose Intolerance in Adults: Biological Mechanism and Dietary Management.
Lactose intolerance in East Indians of Trinidad.
Lactose intolerance in infants, children, and adolescents.
LACTOSE INTOLERANCE WITH NORMAL ACTIVITY OF LACTASE.
Lactose intolerance, lactose malabsorption and genetic predisposition to adult-type hypolactasia in patients after restorative proctocolectomy.
Lactose intolerance.
Lactose intolerance: a non-allergic disorder often managed by allergologists.
Lactose intolerance: a nursing perspective.
Lactose intolerance: analysis of underlying factors.
Lactose intolerance: lactose tolerance test versus genotyping.
Lactose intolerance: problems in diagnosis and treatment.
Lactose malabsorption and intolerance: pathogenesis, diagnosis and treatment.
Lactose malabsorption and intolerance: What should be the best clinical management?
Lactose malabsorption and small-intestinal lactase in normal Chinese children.
Lactose malabsorption in children and adolescents with inflammatory bowel disease.
Lactose malabsorption is associated with early signs of mental depression in females: a preliminary report.
Lactose malabsorption is not a cause of diarrhea during phototherapy.
Lactose malabsorption.
Late-onset hypolactasia and persistent high lactase activity in humans.
Management and treatment of lactose malabsorption.
Management of lactose intolerance.
Milk consumption and lactose intolerance in adults.
Modifying Intestinal Integrity and Micro Biome in Severe Malnutrition with Legume-Based Feeds (MIMBLE 2.0): protocol for a phase II refined feed and intervention trial.
Molecular and cellular aspects and regulation of intestinal lactase-phlorizin hydrolase.
Molecular Characterization and In Vitro Analyses of a Sporogenous Bacterium with Potential Probiotic Properties.
Molecular cloning of a novel cDNA from Mus muscular BALB/c mice encoding glycosyl hydrolase family 1: a homolog of human lactase-phlorizin hydrolase.
Molecular differentiation of congenital lactase deficiency from adult-type hypolactasia.
Molecular genetics of adult-type hypolactasia.
Molecularly defined adult-type hypolactasia among working age people with reference to milk consumption and gastrointestinal symptoms.
Molecularly defined lactose malabsorption, peak bone mass and bone turnover rate in young finnish men.
More evidence for the recessive inheritance of selective adult type lactose malabsorption.
Morphological method for the diagnosis of human adult type hypolactasia.
Mosaic pattern of lactase expression by villous enterocytes in human adult-type hypolactasia.
Mosaic regulation of lactase in human adult-type hypolactasia.
Mucosal function and breath hydrogen excretion: comparative studies in the clinical evaluation of children with nonspecific abdominal complaints.
Noninvasive Diagnosis of Hypolactasia With 4-Galactosylxylose: A Multicentre, Open-Label, Phase IIB-III Nonrandomized Trial.
Nutritional management of lactose intolerance: the importance of diet and food labelling.
ORAL ADMINISTRATION OF EXOGENOUS LACTASE IN TABLETS FOR PATIENTS DIAGNOSED WITH LACTOSE INTOLERANCE DUE TO PRIMARY HYPOLACTASIA.
PCR-RFLP genotyping assay for a lactase persistence polymorphism upstream of the lactase-phlorizin hydrolase gene.
Peroxisome proliferator-activated receptor gamma (PPAR?) regulates lactase expression and activity in the gut.
Pitfalls in LightCycler diagnosis of the single-nucleotide polymorphism 13.9 kb upstream of the lactase gene that is associated with adult-type hypolactasia.
Prebiotics for Lactose Intolerance: Variability in Galacto-Oligosaccharide Utilization by Intestinal Lactobacillus rhamnosus.
Prepubertal subchronic exposure to soy milk and glyphosate leads to endocrine disruption.
Prevalence of lactose intolerance and nutrients intake in an older population regarded as lactase non-persistent.
Prevalence of lactose intolerance in Chile: a double-blind placebo study.
Prevalence of primary adult lactose malabsorption and awareness of milk intolerance in Italy.
Prevalence of primary adult lactose malabsorption in Poland.
Production of volatile fatty acids as a result of bacterial interactions in the cecum of gnotobiotic rats and chickens fed a lactose-containing diet.
Protein patterns of brush-border fragments in congenital lactose malabsorption and in specific hypolactasia of the adult.
Quick test: a new test for the diagnosis of duodenal hypolactasia.
Randomized, double-blind clinical trial of a lactose-free and a lactose-containing formula in dietary management of acute childhood diarrhea.
Recent Advances on Lactose Intolerance: Tolerance Thresholds and Currently Available Solutions.
Regulation of intestinal lactase in adult hypolactasia.
Reinvestigation of lactose intolerant children: lack of correlation between continuing lactose intolerance and small intestinal morphology, disaccharidase activity, and lactose tolerance tests.
Relationships between lactase activity and calcium absorption. Lactose intolerance in hyperparathyroidism.
Review article: lactose intolerance in clinical practice--myths and realities.
Safety and Ethics in Endoscopic Studies in Children: Evidence From the BEECH Study in Zambia.
Selected disorders of malabsorption.
Serum diamine oxidase activity is associated with lactose malabsorption phenotypic variation.
Several different lactase persistence associated alleles and high diversity of the lactase gene in the admixed Brazilian population.
Simple Strategy to Protect Lactase Activity in Solid Formulation.
Single nucleotide polymorphism C/T(-13910), located upstream of the lactase gene, associated with adult-type hypolactasia: validation for clinical practice.
Single-nucleotide polymorphisms and activity analysis of the promoter and enhancer of the pig lactase gene.
Some new and important clues to the causes of colic.
Strip test is reliable in common prevalences of hypolactasia.
Structure of the chromosomal gene and cDNAs coding for lactase-phlorizin hydrolase in humans with adult-type hypolactasia or persistence of lactase.
Study on influence of age, gender and genetic variants on lactose intolerance and its impact on milk intake in adult Asian Indians.
Successful Treatment With Phenobarbital Following Lactase Supplementation in an Infant With Lactose Intolerance.
Surface staining on the villus of lactase protein and lactase activity in adult-type hypolactasia.
T-13910 DNA variant associated with lactase persistence interacts with Oct-1 and stimulates lactase promoter activity in vitro.
The -13914G>A variant upstream of the lactase gene (LCT) is associated with lactase persistence/non-persistence.
The 13C/2H-glucose test for determination of small intestinal lactase activity.
The biosynthetic basis of adult lactase deficiency.
The clinical significance of lactose intolerance.
The Diverse Forms of Lactose Intolerance and the Putative Linkage to Several Cancers.
The effect of oral supplementation with Lactobacillus reuteri or tilactase in lactose intolerant patients: randomized trial.
The Eurasian lactase persistence variant LCT-13910 C/T is associated with vitamin D levels in individuals living at high latitude, more so than exposure to sunlight.
The frequency of the LCT*-13910C>T polymorphism associated with lactase persistence diverges among Euro-descendant groups from Brazil.
The Globalization of Cow's Milk Production and Consumption: Biocultural Perspectives.
The Importance of Lactose in the Human Diet: Outcomes of a Mexican Consensus Meeting.
The molecular basis of lactose intolerance.
The myth of increased lactose intolerance in African-Americans.
The prevalence of lactase deficiency and lactose intolerance in Chinese children of different ages.
The Relationship Between the Human Genome and Microbiome Comes into View.
The role of calcium in human aging.
The role of colonic microbiota in lactose intolerance.
Tinospora cordifolia, a Novel Source of Extracellular Disaccharidases, Useful for Human Disaccharidase Deficiency Therapy.
Transcriptional regulation of the lactase-phlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia.
Triple sugar screen breath hydrogen test for sugar intolerance in children with functional abdominal symptoms.
Use of a Novel Probiotic Formulation to Alleviate Lactose Intolerance Symptoms-a Pilot Study.
Use of genetic testing for hypolactasia trait in the North Denmark Region.
[57-year-old female patient in early retirement with underweight and chronic-relapsing diarrhoea]
[Accuracy of lactase gene C/T-13910 polymorphism and hydrogen breath test in a gastroenterology outpatient clinic: a retrospective study].
[Analysis of lactase activities of small intestine mucous membrane by double labeled stable isotope technique in subjects with lactase deficiency]
[Birth-cohort analysis in adult-type hypolactasia].
[Case of lactose intolerance with normal lactase activities]
[Clinical studies of pediatric malabsorption syndromes]
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
[Correction of dietary lactose intolerance by administration of liquid lactase]
[Determination of lactose intolerance frequency in children with food allergy]
[Determination of milk and diary products consumption and their connection with lactose malabsorption or lactose intolerance in selected disorders of the alimentary tract in children]
[Diagnosing lactose intolerance in adults.]
[Diagnosis and therapy of lactose malabsorption]
[Effect of exogenous lactase on the absorption of lactose and its intolerance symptoms]
[Effects of lactase administration in children with lactose malabsorption. Evaluation using the breath hydrogen test]
[Efficacy and safety of lactase additive in preterm infants with lactose intolerance: a prospective randomized controlled trial].
[Food allergy, food intolerance or functional disorder?]
[Frequency and clinical overview of hypolactasia among children, adolescents and students of Szczecin schools].
[Genogeographic primary hypolactasia in the Old World populations]
[Giardiasis in children with chronic diarrhea. Incidence, growth, clinical symptoms and changes in the small intestine]
[Intestinal lactase and milk consumption before and after gastrectomy]
[Lactase deficiency and lactose intolerance-related symptoms in adult healthy subjects from western France]
[Lactose digestion by milk fermented with Lactobacillus acidophilus and Lactobacillus casei of human origin]
[Lactose intolerance and lactase deficiency in adult patients in Curacao]
[Lactose intolerance caused by lactase deficiency]
[Lactose intolerance in neonates with non-infectious diarrhea].
[Lactose intolerance: changing paradigms due to molecular biology]
[Lactose intolerance: past and present. Part 1].
[Lactose intolerance: pathophysiology, clinical symptoms, diagnosis and treatment]
[Lactose intolerance].
[Lactose malabsorption and -intolerance - who will benefit from a lactose-reduced diet?]
[Lactose tolerance in children with chronic gastroduodenal zone diseases]
[Milk intolerance, lactose intolerance and lactase deficiency in partial resection of the stomach]
[Small intestinal bacterial overgrowth as a cause of lactase deficiency].
[Study on the incidence of lactose intolerance of children in China]
[The influence of the vitamin D3 level in the blood serum of lactase gene polymorphism on the development of chronic polypous rhinosinusitis].
[The treatment of lactose intolerance with lactase]
[Use of enzyme substitutes in hypolactasia]
[Yogurt and dietary recommendations for lactose intolerance].
[Yogurt as source of lactose autodigestion]
Liver Cirrhosis
Lactose malabsorption is a risk factor for decreased bone mineral density in pancreatic insufficient cystic fibrosis patients.
Liver Diseases
Hypolactasia is associated with insulin resistance in nonalcoholic steatohepatitis.
Liver Failure
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Long QT Syndrome
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Lymphadenopathy
Adult T-cell Leukemia/Lymphoma as a Methotrexate-associated Lymphoproliferative Disorder in a Patient with Rheumatoid Arthritis - A Case Report.
Blastic transformation of splenic lymphoma with villous lymphocytes after a well-controlled chronic phase of more than 10 years.
Lymphoma
Celiac sprue among US military veterans: associated disorders and clinical manifestations.
Prognostic value of C-reactive protein, lactase dehydrogenase and anemia in recurrent or refractory aggressive lymphoma.
Malabsorption Syndromes
A comparative study of lactase and sucrase-isomaltase activities and immunoreactivities in jejunal biopsies of patients suffering from the malabsorption syndrome.
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Suitability of the azocoupling reaction with 1-naphthyl-beta-D-glucoside for the histochemical demonstration of lactase (lactase-beta-glucosidase complex) in human enterobiopsies.
[L-alanyl-L-proline-dipeptidase and glycyl-L-valine-depeptidase in malabsorption syndrome]
[Malabsorption of carbohydrates in children (author's transl)]
[Malabsorption syndrome as a result of lactase deficiency in combination with fructose intolerance]
Malaria
Demographic history and admixture dynamics in African Sahelian populations.
Did malaria select for primary adult lactase deficiency?
Lactase deficiency phenotype has not been selected by malaria.
Lactase persistence genotypes and malaria susceptibility in Fulani of Mali.
Lactose absorption in patients with glucose 6-phosphate dehydrogenase deficiency with and without favism.
Primary lactase deficiency and past malarial endemicity in Sardinia.
The Genetic Legacy of the Indian Ocean Slave Trade: Recent Admixture and Post-admixture Selection in the Makranis of Pakistan.
The sensitivity of the OptiMAL rapid diagnostic test to the presence of Plasmodium falciparum gametocytes compromises its ability to monitor treatment outcomes in an area of Papua New Guinea in which malaria is endemic.
Malnutrition
Congenital lactose intolerance is triggered by severe mutations on both alleles of the lactase gene.
Effect of an episode of severe malnutrition and age on lactose absorption by recovered infants and children.
Effect of prenatal exposure to ethanol on intestinal development of rat fetuses.
Effects of malnutrition on expression and activity of lactase in children.
Jejunal disaccharidases in protein energy malnutrition and recovery.
Lactose intolerance among severely malnourished children with diarrhoea admitted to the nutrition unit, Mulago hospital, Uganda.
Moderate and severe protein energy malnutrition in childhood: effects on jejunal mucosal morphology and disaccharidase activities.
Regulation of lactase and sucrase-isomaltase gene expression in the duodenum during childhood.
Marfan Syndrome
[Clinical effectiveness of the therapeutic nutrition of sick children using enteral feeding preparations and low-lactose mixtures]
Melanoma
Biochemical characterization of three hamster melanoma variants--II. Glycolysis and oxygen consumption.
Evolutionary triangulation: informing genetic association studies with evolutionary evidence.
Mesothelioma
[Diagnostic contribution of the determination of CEA, pH, glucose and lactase dehydrogenase in the pleural fluid in patients with mesothelioma]
Metabolic Syndrome
Associations between lactase persistence and the metabolic syndrome in a cross-sectional study in the Canary Islands.
Gene-environment interactions in human health: case studies and strategies for developing new paradigms and research methodologies.
The lactase persistence genotype is a protective factor for the metabolic syndrome.
Microsporidiosis
Mucosal abnormalities in microsporidiosis.
Migraine Disorders
Elevated IgM in dietary migraine with lactase deficiency.
Milk Hypersensitivity
Allergy to cow's milk in the first year of life and its prevention.
Diagnostic algorithm and peculiarities of monitoring for infants with disorders of the gastrointestinal tract.
Food hypersensitivity allergy or malabsorption.
Milk protein-free diet for nonseasonal asthma and migraine in lactase-deficient patients.
Molecularly defined adult-type hypolactasia in school-aged children with a previous history of cow's milk allergy.
Multiple Myeloma
The detection of circulating plasma cells may improve the Revised International Staging System (R-ISS) risk stratification of patients with newly diagnosed multiple myeloma.
Multiple Sclerosis
Geographic associations between lactase phenotype, multiple sclerosis, and inflammatory bowel diseases; Does obesity trump geography?
Muscle Cramp
Intestinal pH and propulsion: an explanation of diarrhoea in lactase deficiency and laxation by lactulose.
Small intestinal lactase status, frequency distribution of enzyme activity and milk intake in a multi-ethnic population.
Myocardial Infarction
Milk intake is not associated with ischaemic heart disease in observational or Mendelian randomization analyses in 98,529 Danish adults.
Neoplasm Metastasis
Prognostic value of a computer-aided diagnosis system involving bone scans among men treated with docetaxel for metastatic castration-resistant prostate cancer.
Neoplasms
Ampicillin-improved glucose tolerance in diet-induced obese C57BL/6NTac mice is age dependent.
Association of LCT-13910 C/T Polymorphism and Colorectal Cancer.
Diarrhea.
Enzyme activities in biopsy specimens from large-bowel mucosa in colorectal adenomas and carcinomas.
Expression and different polarity of aminopeptidase N in normal human colonic mucosa and colonic tumors.
Expression of p53, c-Myc, or Bcl-6 suggests a poor prognosis in primary central nervous system diffuse large B-cell lymphoma among immunocompetent individuals.
Genetic variation in the lactase gene, dairy product intake and risk for prostate cancer in the European prospective investigation into cancer and nutrition.
Increased cell surface EGF receptor expression during the butyrate-induced differentiation of human HCT-116 colon tumor cell clones.
Intestinal brush-border-associated enzymes: co-ordinated expression in colorectal cancer.
Lactase dehydrogenase as a tumor marker for recurrent disease in Ewing's sarcoma.
Lactase persistence and bitter taste response: instrumental variables and mendelian randomization in epidemiologic studies of dietary factors and cancer risk.
Predictors for postoperative renal function after open partial nephrectomy: Including postoperative biomarkers.
Probiotics and medical nutrition therapy.
Protective effects of N(2)?L?alanyl?L?glutamine mediated by the JAK2/STAT3 signaling pathway on myocardial ischemia reperfusion.
Regulation of sucrase-isomaltase gene expression in human intestinal epithelial cells by inflammatory cytokines.
[Frequent causes of diarrhea: celiac disease and lactose intolerance]
[The use of parietal pH-metry in the diagnosis of intestinal diseases]
Nephrocalcinosis
Hypercalcemia and nephrocalcinosis in patients with congenital lactase deficiency.
Neural Tube Defects
Maternal Lactase Polymorphism (rs4988235) Is Associated with Neural Tube Defects in Offspring in the National Birth Defects Prevention Study.
Non-alcoholic Fatty Liver Disease
Hypolactasia is associated with insulin resistance in nonalcoholic steatohepatitis.
Noonan Syndrome
Genetic counseling and parental self-concept change.
Obesity
Age-related changes in sucrase and lactase activity in the small intestine of 3- and 10-week-old obese mice (C57BL/6Jobob).
Association of lactase persistence genotype with milk consumption, obesity and blood pressure: a Mendelian randomization study in the 1982 Pelotas (Brazil) Birth Cohort, with a systematic review and meta-analysis.
Association of the European Lactase Persistence Variant (LCT-13910 C>T Polymorphism) with Obesity in the Canary Islands.
Association of the LCT-13910C>T Polymorphism With Obesity and Its Modulation by Dairy Products in a Mediterranean Population.
European lactase persistence genotype shows evidence of association with increase in body mass index.
Genotype C/C 13910 of the Lactase Gene as a Risk Factor for the Formation of Insulin-Resistant Obesity in Children.
Geographic associations between lactase phenotype, multiple sclerosis, and inflammatory bowel diseases; Does obesity trump geography?
Global associations of national economic wealth are more robust with inflammatory bowel diseases than with obesity.
Inhibitory effects of estrogens on digestive enzymes, insulin deficiency, and pancreas toxicity in diabetic rats.
Relation of the C/T-13910 LCT Polymorphism with Body Composition Measures and Their Modulation by Dairy Products in a Caucasian Men.
Relationship(s) between obesity and inflammatory bowel diseases: possible intertwined pathogenic mechanisms.
The lactase -13910C>T polymorphism (rs4988235) is associated with overweight/obesity and obesity-related variables in a population sample of Portuguese young adults.
The lactase rs4988235 is associated with obesity related variables and diabetes mellitus in menopausal obese females.
Treatment of lactase deficiency in children's obesity with genotype c/c 13910 of lactase gene.
Obesity, Abdominal
The lactase persistence -13910C>T polymorphism shows indication of association with abdominal obesity among Portuguese children.
oligo-1,6-glucosidase deficiency
Clinical Characteristics of Disaccharidase Deficiencies Among Children Undergoing Upper Endoscopy.
Demographic and Clinical Correlates of Mucosal Disaccharidase Deficiencies in Children With Functional Dyspepsia.
Disaccharidase activity in male and female C57BL/6 mice infected with Giardia muris.
Intestinal disaccharidase activities in relation to age, race, and mucosal damage.
Lactase and other disaccharidase deficiencies in a hospital population.
Prevalence of Disaccharidase Deficiency in Adults With Unexplained Gastrointestinal Symptoms.
Relationships between disaccharidase deficiencies, duodenal inflammation and symptom profile in children with abdominal pain.
Selective lactase deficiency is common in pediatric patients undergoing upper endoscopy.
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
[Intestinal disaccharidase and alkaline phosphatase activities of jejunal biopsies in small bowel diseases of children (author's transl)]
Osteomalacia
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
Osteoporosis
Adult lactose intolerance, calcium intake, bone metabolism and bone density in German-Turkish immigrants.
Differences between lactase deficient and non-lactase deficient women with spinal osteoporosis.
Does lactose intolerance predispose to low bone density? A population-based study of perimenopausal Finnish women.
First reported case of lysinuric protein intolerance (LPI) in Lithuania, confirmed biochemically and by DNA analysis.
Genetic predisposition for adult lactose intolerance and relation to diet, bone density, and bone fractures.
Genetically predicted milk consumption and bone health, ischemic heart disease and type 2 diabetes: a Mendelian randomization study.
High osteoporosis risk among East Africans linked to lactase persistence genotype.
Human adult-onset lactase decline: an update.
Increased serum osteocalcin levels in patients with lactase deficiency.
Intestinal lactase activity and calcium absorption in the aging female with osteoporosis.
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
Lactase deficiency in osteoporosis.
Lactase deficiency: prevalence in osteoporosis.
Lactose intolerance and osteoporosis in men.
Nutrition in prevention of osteoporosis.
Osteoporosis and primary intestinal lactase deficiency.
Osteoporosis risk of the subjects with isolated lactase enzyme deficiency.
Osteoporosis, intestinal lactase deficiency and low dietary calcium intake.
[Incidence of lactase deficiency in patients with involution osteoporosis and in normal subjects. Its effect on the nutritional intake of calcium and phosphorus]
[Incidence of lactose intolerance in postmenopausal osteoporosis]
Osteoporosis, Postmenopausal
Association Between Polymorphisms of VDR, COL1A1, and LCT Genes and Bone Mineral Density in Belarusian Women With Severe Postmenopausal Osteoporosis.
Lactase deficiency: prevalence in osteoporosis.
Lactose and calcium absorption in postmenopausal osteoporosis.
[Incidence of lactase deficiency in patients with involution osteoporosis and in normal subjects. Its effect on the nutritional intake of calcium and phosphorus]
Ovarian Neoplasms
Lactase persistence and milk consumption as determinants of ovarian cancer risk.
Lactose absorption in patients with ovarian cancer.
Lactose and galactose intake and metabolism in relation to the risk of epithelial ovarian cancer.
Pancreatitis
[Lactase activity in the small intestine in experimental pancreatitis]
[Lactase activity of the mucous membrane of the small intestine of dogs with experimental pancreatitis]
Pancreatitis, Chronic
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
[14CO2 exhalation tests. Diagnostic improvement in gastroenterologic diseases]
Parasitic Diseases
Molecular and cellular aspects and regulation of intestinal lactase-phlorizin hydrolase.
[Digestive parasitic diseases and lactase deficiency in children]
Paratuberculosis
Lactase persistence, NOD2 status and Mycobacterium avium subsp. paratuberculosis infection associations to Inflammatory Bowel Disease.
Peptic Ulcer
[Lactase insufficiency in patients with gastroduodenal ulcer in the evolutive stage]
Plague
Ancient DNA analysis reveals high frequency of European lactase persistence allele (T-13910) in medieval central europe.
Porphyrias, Hepatic
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Prader-Willi Syndrome
Genetic counseling and parental self-concept change.
Proctocolitis
Diagnostic algorithm and peculiarities of monitoring for infants with disorders of the gastrointestinal tract.
Prostatic Neoplasms
Association of the Lactase Persistence Haplotype Block With Disease Risk in Populations of European Descent.
Genetic variation in the lactase gene, dairy product intake and risk for prostate cancer in the European prospective investigation into cancer and nutrition.
Lactase persistence, dietary intake of milk, and the risk for prostate cancer in Sweden and Finland.
The Diverse Forms of Lactose Intolerance and the Putative Linkage to Several Cancers.
Protein Deficiency
[Effect of protein deficiency in the female rat diet during pregnancy and lactation on the activity of the membrane and soluble forms of digestive enzymes in the offspring small intestine]
Protein-Energy Malnutrition
Intestinal disaccharidases in malnourished infant rats.
Lactose intolerance among severely malnourished children with diarrhoea admitted to the nutrition unit, Mulago hospital, Uganda.
Moderate and severe protein energy malnutrition in childhood: effects on jejunal mucosal morphology and disaccharidase activities.
Protein-Losing Enteropathies
Protein-losing enteropathy following the Fontan procedure in a child with intestinal lactase deficiency treated with lactose-free diet.
Proteinuria
[New cases of celiac disease detected by anti-endomysial antibody test in families of gluten-sensitive patients and among children examined for non-specific gastrointestinal complaints]
Pruritus
Lactase deficiency: a potential novel aetiological factor in chronic pruritus of unknown origin.
Rectal Prolapse
Thyrotoxicosis in a neonate of a mother with no history of thyroid disease.
Renal Insufficiency
Predictors for postoperative renal function after open partial nephrectomy: Including postoperative biomarkers.
Renal Insufficiency, Chronic
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Rhinitis
Congenital lymphangiectasia and atopy.
Occupational sensitization to lactase in the dietary supplement industry.
Rickets
Lactase activity in experimental rickets and vitamin D intoxication.
[New cases of celiac disease detected by anti-endomysial antibody test in families of gluten-sensitive patients and among children examined for non-specific gastrointestinal complaints]
Rotavirus Infections
An NSP4-dependant mechanism by which rotavirus impairs lactase enzymatic activity in brush border of human enterocyte-like Caco-2 cells.
Differential tropism of EB rotavirus (serotype 3) to small intestine of homologous murine model.
Effect of orally administered epidermal growth factor on intestinal recovery of neonatal pigs infected with rotavirus.
Intestinal changes associated with rotavirus and enterotoxigenic Escherichia coli infection in calves.
Is lactase the receptor and uncoating enzyme for infantile enteritis (rota) viruses?
Lack of protection from rotavirus infection in children with congenital intestinal lactase deficiency.
Randomized, double-blind clinical trial of a lactose-free and a lactose-containing formula in dietary management of acute childhood diarrhea.
Sarcoma, Ewing
Lactase dehydrogenase as a tumor marker for recurrent disease in Ewing's sarcoma.
Schistosomiasis mansoni
Lactase deficiency in patients with intestinal schistosomiasis.
Sepsis
Extrauterine growth restriction in preterm infants: importance of optimizing nutrition in neonatal intensive care units.
Shwachman-Diamond Syndrome
Selected disorders of malabsorption.
Sprue, Tropical
Persistent deficiency of intestinal lactase in apparently cured tropical sprue.
Starvation
Adaptation of intestinal hydrolases to starvation in rats: effect of thyroid function.
Dependency of lactose absorption on lactase activity in starved rats.
Dietary sucrose enhances intestinal lactase gene expression in euthyroid rats.
Different effect of starvation on activity of sucrase and lactase in rat jejunoileum.
Discrepancy between the intestinal lactase enzymatic activity and mRNA accumulation in sucklings and adults. Effect of starvation and thyroxine treatment.
Effect of starvation on small intestinal enzyme activity in germ-free rats.
Effects of starvation and refeeding on jejunal disaccharidase activity.
Lactase activity is under hormonal control in the intestine of adult rat.
Lactase expression is controlled differently in the jejunum and ileum during development in rats.
Modifications of brush border enzyme activities during starvation in the jejunum and ileum of adult rats.
Modulation by thyroxine of the amount of lactase protein in the jejunum of adult rats.
Refeeding after starvation in the rat: comparative effects of lipids, proteins and carbohydrates on jejunal and ileal mucosal adaptation.
Relationship between the changes in gastrin levels and intestinal properties in the starved rat.
Stimulation of lactase synthesis induced by starvation in the jejunum of adult rat.
Steatorrhea
Human immunodeficiency virus infection of enterocytes and mononuclear cells in human jejunal mucosa.
sucrose alpha-glucosidase deficiency
Clinical Characteristics of Disaccharidase Deficiencies Among Children Undergoing Upper Endoscopy.
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
Ethnic differences in intestinal disaccharidase values in children in Finland.
Intestinal disaccharidases in Greenland Eskimos.
Molecular aspects of disaccharidase deficiencies.
Selected disorders of malabsorption.
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
[Intestinal disaccharidase and alkaline phosphatase activities of jejunal biopsies in small bowel diseases of children (author's transl)]
[Useful and superfluous measures in the treatment of infant diarrhea]
Thalassemia
Asian and Pacific Islander Americans: An Overview of Demographic Characteristics and Health Care Issues.
Thyroiditis, Autoimmune
Effects of low-carbohydrate diet therapy in overweight subjects with autoimmune thyroiditis: possible synergism with ChREBP.
Thyrotoxicosis
Thyrotoxicosis in a neonate of a mother with no history of thyroid disease.
Trypanosomiasis, African
Food and pathogen adaptations in the Angolan Namib desert: Tracing the spread of lactase persistence and human African trypanosomiasis resistance into southwestern Africa.
Tuberculosis
Asian and Pacific Islander Americans: An Overview of Demographic Characteristics and Health Care Issues.
Uremia
Activities of intestinal enzymes in experimental chronic renal insufficiency.
Urticaria
Familial aquagenic urticaria associated with familial lactose intolerance.
Vasculitis
A randomized multicenter clinical trial to evaluate the efficacy of melatonin in the prophylaxis of SARS-CoV-2 infection in high-risk contacts (MeCOVID Trial): A structured summary of a study protocol for a randomised controlled trial.
Virus Diseases
Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial).
Vitamin D Deficiency
Digestive and nutritional considerations in celiac disease: could supplementation help?
Whipple Disease
Disorders of intestinal secretion and absorption.