Disease on EC 3.2.1.48 - sucrose alpha-glucosidase
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Adenocarcinoma
Abundant expression of the intestinal protein villin in Barrett's metaplasia and esophageal adenocarcinomas.
Adenocarcinoma
Detection of Barrett's adenocarcinoma of the gastric cardia with sucrase isomaltase and p53.
Adenocarcinoma
Expression of enzymatically active sucrase-isomaltase is a ubiquitous property of colon adenocarcinomas.
Adenocarcinoma
Gene expression profiling of Caco-2 BBe cells suggests a role for specific signaling pathways during intestinal differentiation.
Adenocarcinoma
Sucrase-isomaltase expression and enterocytic ultrastructure of human colorectal tumors.
Adenocarcinoma
Sucrase-isomaltase gene expression in Barrett's esophagus and adenocarcinoma.
Adenocarcinoma
Sucrase-isomaltase: a marker associated with the progression of adenomatous polyps to adenocarcinomas.
Adenomatous Polyps
Sucrase-isomaltase: a marker associated with the progression of adenomatous polyps to adenocarcinomas.
Alkaptonuria
Alcaptonuria and sucrase-isomaltase deficiency in three offspring of a consanguineous marriage.
alpha,alpha-trehalase deficiency
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
Barrett Esophagus
Sucrase-isomaltase gene expression in Barrett's esophagus and adenocarcinoma.
beta-fructofuranosidase deficiency
Molecular cloning of sucrase-isomaltase cDNA in the house musk shrew Suncus murinus and identification of a mutation responsible for isolated sucrase deficiency.
beta-fructofuranosidase deficiency
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
Carcinoma
A and H blood group antigens as markers of sucrase-isomaltase from the enterocyte-like differentiated human colon carcinoma cell lines HT-29 and Caco-2.
Carcinoma
A limited upstream region of the human sucrase-isomaltase gene confers glucose-regulated expression on a heterologous gene.
Carcinoma
Clonal analysis of sucrase-isomaltase expression in the human colon adenocarcinoma Caco-2 cells.
Carcinoma
Expression of enzymatically active sucrase-isomaltase is a ubiquitous property of colon adenocarcinomas.
Carcinoma
Intracellular localization and endocytosis of brush border enzymes in the enterocyte-like cell line Caco-2.
Carcinoma
Sucrase-isomaltase: a marker associated with the progression of adenomatous polyps to adenocarcinomas.
Carcinoma
Sucrase-isomaltase: a marker of foetal and malignant epithelial cells of the human colon.
Carcinoma
The biosynthesis of intestinal sucrase-isomaltase in human embryo is most likely controlled at the level of transcription.
Carcinoma
Villin, intestinal brush border hydrolases and keratin polypeptides in intestinal metaplasia and gastric cancer; an immunohistologic study emphasizing the different degrees of intestinal and gastric differentiation in signet ring cell carcinomas.
Carcinoma
[Do immunologic markers facilitate differentiation between histologic types of stomach cancer?]
Celiac Disease
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Colitis, Ulcerative
Prospective evaluation of early morphological changes in pelvic ileal pouches.
Colitis, Ulcerative
Protracted diarrhoea in infancy. Analysis of 82 cases with particular reference to diagnosis and management.
Colitis, Ulcerative
Sucrase-isomaltase expression in chronic ulcerative colitis and dysplasia.
Colonic Neoplasms
A and H blood group antigens as markers of sucrase-isomaltase from the enterocyte-like differentiated human colon carcinoma cell lines HT-29 and Caco-2.
Colonic Neoplasms
A potential anti-tumor effect of leukotriene C4 through the induction of 15-hydroxyprostaglandin dehydrogenase expression in colon cancer cells.
Colonic Neoplasms
Clonal analysis of sucrase-isomaltase expression in the human colon adenocarcinoma Caco-2 cells.
Colonic Neoplasms
Differentiation-dependent induction of CYP1A1 in cultured rat small intestinal epithelial cells, colonocytes, and human colon carcinoma cells: basement membrane-mediated apoptosis.
Colonic Neoplasms
Dissection of the asynchronous transport of intestinal microvillar hydrolases to the cell surface.
Colonic Neoplasms
Endocytosis, recycling, and lysosomal delivery of brush border hydrolases in cultured human intestinal epithelial cells (Caco-2).
Colonic Neoplasms
Expression of enzymatically active sucrase-isomaltase is a ubiquitous property of colon adenocarcinomas.
Colonic Neoplasms
Immunohistological evidence, obtained with monoclonal antibodies, of small intestinal brush border hydrolases in human colon cancers and foetal colons.
Colonic Neoplasms
Inhibition of laminin alpha 1-chain expression leads to alteration of basement membrane assembly and cell differentiation.
Colonic Neoplasms
Intrinsically disordered human C/EBP homologous protein regulates biological activity of colon cancer cells during calcium stress.
Colonic Neoplasms
Lactase and sucrase-isomaltase gene expression during Caco-2 cell differentiation.
Colonic Neoplasms
Sequence of the complete cDNA and the 5' structure of the human sucrase-isomaltase gene. Possible homology with a yeast glucoamylase.
Colonic Neoplasms
Sucrase-isomaltase in colon cancers: an example of re-expression of a foetal enzyme with associated blood group antigens.
Colonic Neoplasms
The processing of asparagine-linked oligosaccharides in HT-29 cells is a function of their state of enterocytic differentiation. An accumulation of Man9,8-GlcNAc2-Asn species is indicative of an impaired N-glycan trimming in undifferentiated cells.
Colorectal Neoplasms
Association between sucrase-isomaltase and p53 expression in colorectal cancer.
Colorectal Neoplasms
Intestinal brush-border-associated enzymes: co-ordinated expression in colorectal cancer.
Colorectal Neoplasms
Sucrase-isomaltase and other brush border glycosidases in colorectal tumors.
Colorectal Neoplasms
Sucrase-isomaltase expression and enterocytic ultrastructure of human colorectal tumors.
Colorectal Neoplasms
Sucrase-isomaltase is an independent prognostic marker for colorectal carcinoma.
Congenital Abnormalities
The multiple roles of sucrase-isomaltase in the intestinal physiology.
Cystic Fibrosis
Anomalous apical plasma membrane phenotype in CK8-deficient mice indicates a novel role for intermediate filaments in the polarization of simple epithelia.
Cystic Fibrosis
Microvillus inclusion disease: a genetic defect affecting apical membrane protein traffic in intestinal epithelium.
Cystic Fibrosis
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Cystic Fibrosis
Transimmortalized mouse intestinal cells (m-ICc12) that maintain a crypt phenotype.
Cytomegalovirus Infections
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Diabetes Complications
MiR-26a and miR-26b downregulate the expression of sucrase-isomaltase enzyme: A new chapter in diabetes treatment.
Diabetes Mellitus
Bioactive compounds in plant materials for the prevention of diabetesand obesity.
Diabetes Mellitus
Disordered expression of the sucrase-isomaltase complex in the small intestine in Otsuka Long-Evans tokushima fatty rats, a model of non-insulin-dependent diabetes mellitus with insulin resistance.
Diabetes Mellitus
Morphological changes and increased sucrase and isomaltase activity in small intestines of insulin-deficient and type 2 diabetic rats.
Diabetes Mellitus, Experimental
The intestinal brush border membrane in diabetes. Studies of sucrase-isomaltase metabolism in rats with streptozotocin diabetes.
Diabetes Mellitus, Type 1
Suppressive effect of insulin on the synthesis of sucrase-isomaltase complex in small intestinal epithelial cells, and abnormal increase in the complex under diabetic conditions.
Diabetes Mellitus, Type 2
Bioactive compounds in plant materials for the prevention of diabetesand obesity.
Diabetes Mellitus, Type 2
Disordered expression of the sucrase-isomaltase complex in the small intestine in Otsuka Long-Evans tokushima fatty rats, a model of non-insulin-dependent diabetes mellitus with insulin resistance.
Enteritis
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Enterocolitis
Uncommon causes of postoperative chronic diarrhoea mimicking enterocolitis in Hirschsprung's disease: is there a role for digestive endoscopy?
Ganglioneuroma
Protracted diarrhoea in infancy. Analysis of 82 cases with particular reference to diagnosis and management.
Gastroenteritis
Complex carbohydrate intolerance: diagnostic pitfalls and approach to management.
Gastrointestinal Diseases
Immunoelectrophoretic studies on human small intestinal brush border proteins. A quantitative study of brush border enzymes from single small intestinal biopsies.
Gastrointestinal Diseases
Sucrase-Isomaltase Gene Variants in Patients with Abnormal Sucrase Activity and Functional GI Disorders.
Gastrointestinal Diseases
The Role of Disaccharidase Deficiencies in Functional Abdominal Pain Disorders-A Narrative Review.
Genetic Diseases, Inborn
Congenital sucrase-isomaltase deficiency: an under-diagnosed disease in Chinese children.
Genetic Diseases, Inborn
Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients.
Genetic Diseases, Inborn
The patient journey to diagnosis and treatment of congenital sucrase-isomaltase deficiency.
Giardiasis
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Hirschsprung Disease
Persistent diarrhea due to sucrase-isomaltase deficiency in a postoperative child with Hirschsprung's disease.
Hirschsprung Disease
Protracted diarrhoea in infancy. Analysis of 82 cases with particular reference to diagnosis and management.
Hypercalcemia
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
Hyperglycemia
Biological interaction of newly synthesized astaxanthin-s-allyl cysteine biconjugate with Saccharomyces cerevisiae and mammalian ?-glucosidase: In vitro kinetics and in silico docking analysis.
Hyperglycemia
Hyperglycemia induces intestinal sucrase activity in subtotally pancreatectomized rats.
Hyperglycemia
In Vitro and in Vivo Anti-Hyperglycemic Activities of Taxifolin and Its Derivatives Isolated from Pigmented Rice (Oryzae sativa L. cv. Superhongmi).
Hyperglycemia
Morphological changes and increased sucrase and isomaltase activity in small intestines of insulin-deficient and type 2 diabetic rats.
Infections
Alterations in enzymatic activities of the intestinal mucosa during the course of Giardia lamblia infection in mice.
Infections
Impairments in enzyme activity and biosynthesis of brush border-associated hydrolases in human intestinal Caco-2/TC7 cells infected by members of the Afa/Dr family of diffusely adhering Escherichia coli.
Infections
Small intestinal sucrase activity during experimental infections with Nippostrongylus brasiliensis and/or Eimeria nieschulzi in rats.
Infections
Staphylococcus aureus Infection Influences the Function of Intestinal Cells by Altering the Lipid Raft-Dependent Sorting of Sucrase-Isomaltase.
Inflammatory Bowel Diseases
Sucrase-isomaltase: a marker associated with the progression of adenomatous polyps to adenocarcinomas.
Inflammatory Bowel Diseases
Uncommon causes of postoperative chronic diarrhoea mimicking enterocolitis in Hirschsprung's disease: is there a role for digestive endoscopy?
Insulin Resistance
Disordered expression of the sucrase-isomaltase complex in the small intestine in Otsuka Long-Evans tokushima fatty rats, a model of non-insulin-dependent diabetes mellitus with insulin resistance.
Intestinal Pseudo-Obstruction
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Iron Overload
Immunological analysis of beta-thalassemic mouse intestinal proteins reveals up-regulation of sucrase-isomaltase in response to iron overload.
Irritable Bowel Syndrome
Differential Effects of Sucrase-Isomaltase Mutants on Its Trafficking and Function in Irritable Bowel Syndrome: Similarities to Congenital Sucrase-Isomaltase Deficiency.
Irritable Bowel Syndrome
Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome.
Irritable Bowel Syndrome
Increased Prevalence of Rare Sucrase-isomaltase (SI) Pathogenic Variants in Irritable Bowel Syndrome Patients.
Irritable Bowel Syndrome
Rare Hypomorphic Sucrase Isomaltase Variants in Relation to Irritable Bowel Syndrome Risk in UK Biobank.
Irritable Bowel Syndrome
Sucrase-Isomaltase Deficiency as a Potential Masquerader in Irritable Bowel Syndrome.
lactase deficiency
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
lactase deficiency
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
lactase deficiency
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
lactase deficiency
[Intestinal disaccharidase and alkaline phosphatase activities of jejunal biopsies in small bowel diseases of children (author's transl)]
Lactose Intolerance
Congenital sucrase and isomaltase deficiency with temporary lactose intolerance.
Lactose Intolerance
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
Lactose Intolerance
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.
Lactose Intolerance
Value of breath hydrogen analysis in management of diarrheal illness in childhood: comparison with duodenal biopsy.
Leukemia
Human chromosome 3 and pig chromosome 13 show complete synteny conservation but extensive gene-order differences.
Leukemia
Mapping HSA 3 loci in cattle: additional support for the ancestral synteny of HSA 3 and 21.
Leukemia, Lymphocytic, Chronic, B-Cell
Functional analysis of sucrase-isomaltase mutations from chronic lymphocytic leukemia patients.
Malabsorption Syndromes
A comparative study of lactase and sucrase-isomaltase activities and immunoreactivities in jejunal biopsies of patients suffering from the malabsorption syndrome.
Malnutrition
Effect of pre- & post-weaning protein energy malnutrition on intestinal sucrase & maltase in rats.
Malnutrition
Regulation of lactase and sucrase-isomaltase gene expression in the duodenum during childhood.
Muscle Cramp
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
Muscle Cramp
Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency.
Neoplasm Metastasis
Expression of enzymatically active sucrase-isomaltase is a ubiquitous property of colon adenocarcinomas.
Neoplasms
A and H blood group antigens as markers of sucrase-isomaltase from the enterocyte-like differentiated human colon carcinoma cell lines HT-29 and Caco-2.
Neoplasms
Bioactive compounds in plant materials for the prevention of diabetesand obesity.
Neoplasms
Detection and characterization of sucrase-isomaltase in adult human colon and in colonic polyps.
Neoplasms
Enterocytic columnar non-goblet cells of Barrett's esophagus--an immunohistochemical demonstration of association with malignant evolution.
Neoplasms
Expression of enzymatically active sucrase-isomaltase is a ubiquitous property of colon adenocarcinomas.
Neoplasms
Intestinal brush-border-associated enzymes: co-ordinated expression in colorectal cancer.
Neoplasms
Posttranslational regulation of sucrase-isomaltase expression in intestinal crypt and villus cells.
Neoplasms
Sucrase-isomaltase expression and enterocytic ultrastructure of human colorectal tumors.
Neoplasms
Sucrase-isomaltase: a marker of foetal and malignant epithelial cells of the human colon.
Neoplasms
Use of a monoclonal antibody to sucrase-isomaltase for evaluation of the columnar cuff after stapled restorative proctocolectomy.
Neoplasms
[Do immunologic markers facilitate differentiation between histologic types of stomach cancer?]
Nephrocalcinosis
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
oligo-1,6-glucosidase deficiency
Adult onset sucrase-isomaltase deficiency with secondary disaccharidase deficiency resulting from severe dietary carbohydrate restriction.
oligo-1,6-glucosidase deficiency
Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency.
oligo-1,6-glucosidase deficiency
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
oligo-1,6-glucosidase deficiency
[Intestinal disaccharidase and alkaline phosphatase activities of jejunal biopsies in small bowel diseases of children (author's transl)]
Pneumonia, Staphylococcal
Protracted diarrhoea in infancy. Analysis of 82 cases with particular reference to diagnosis and management.
Protein-Energy Malnutrition
Effect of pre- & post-weaning protein energy malnutrition on intestinal sucrase & maltase in rats.
Rotavirus Infections
Rotavirus infection reduces sucrase-isomaltase expression in human intestinal epithelial cells by perturbing protein targeting and organization of microvillar cytoskeleton.
Staphylococcal Infections
Staphylococcus aureus Infection Influences the Function of Intestinal Cells by Altering the Lipid Raft-Dependent Sorting of Sucrase-Isomaltase.
Starvation
Effect of fasting on the structure and function of the gastrointestinal tract of house sparrows (Passer domesticus).
Starvation
Precocious and reversible expression of sucrase-isomaltase unrelated to intestinal cell turnover.
sucrose alpha-glucosidase deficiency
13C-breath tests for sucrose digestion in congenital sucrase isomaltase-deficient and sacrosidase-supplemented patients.
sucrose alpha-glucosidase deficiency
13C-Labeled-Starch Breath Test in Congenital Sucrase-isomaltase Deficiency.
sucrose alpha-glucosidase deficiency
50 years of progress since congenital sucrase-isomaltase deficiency recognition.
sucrose alpha-glucosidase deficiency
A glutamine to proline exchange at amino acid residue 1098 in sucrase causes a temperature-sensitive arrest of sucrase-isomaltase in the endoplasmic reticulum and cis-Golgi.
sucrose alpha-glucosidase deficiency
A mutation in a highly conserved region in brush-border sucrase-isomaltase and lysosomal alpha-glucosidase results in Golgi retention.
sucrose alpha-glucosidase deficiency
A phenylalanine-based folding determinant in intestinal sucrase-isomaltase that functions in the context of a quality control mechanism beyond the endoplasmic reticulum.
sucrose alpha-glucosidase deficiency
A study of the molecular pathology of sucrase-isomaltase deficiency. A defect in the intracellular processing of the enzyme.
sucrose alpha-glucosidase deficiency
Adult onset sucrase-isomaltase deficiency with secondary disaccharidase deficiency resulting from severe dietary carbohydrate restriction.
sucrose alpha-glucosidase deficiency
Alcaptonuria and sucrase-isomaltase deficiency in three offspring of a consanguineous marriage.
sucrose alpha-glucosidase deficiency
Altered folding, turnover, and polarized sorting act in concert to define a novel pathomechanism of congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Breath hydrogen test and sucrase isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Catalytically inactive sucrase antigen of rabbit small intestine: the enzyme precursor.
sucrose alpha-glucosidase deficiency
Clinical and Histopathologic Predictors of Disaccharidase Deficiency in Duodenal Biopsy Specimens.
sucrose alpha-glucosidase deficiency
Clinical aspects and treatment of congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Clinical Characteristics of Disaccharidase Deficiencies Among Children Undergoing Upper Endoscopy.
sucrose alpha-glucosidase deficiency
Clinical heterogeneity in congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Combined assessment of intestinal disaccharidases in congenital asucrasia by differential urinary disaccharide excretion.
sucrose alpha-glucosidase deficiency
Complex carbohydrate intolerance: diagnostic pitfalls and approach to management.
sucrose alpha-glucosidase deficiency
Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Congenital and Putatively Acquired Forms of Sucrase-isomaltase Deficiency in Infancy: Effects of Sacrosidase Therapy.
sucrose alpha-glucosidase deficiency
Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives.
sucrose alpha-glucosidase deficiency
Congenital sucrase and isomaltase deficiency with temporary lactose intolerance.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency. Observations over a period of 6 years.
sucrose alpha-glucosidase deficiency
Congenital Sucrase-isomaltase Deficiency: A Novel Compound Heterozygous Mutation Causing Aberrant Protein Localization.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency: an under-diagnosed disease in Chinese children.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency: diagnostic challenges and response to enzyme replacement therapy.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency: diet assessment and education guidelines.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency: heterogeneity of inheritance, trafficking, and function of an intestinal enzyme complex.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.
sucrose alpha-glucosidase deficiency
Congenital sucrase-isomaltase deficiency: summary of an evaluation in one family.
sucrose alpha-glucosidase deficiency
Deletion of enzyme protein from the brush border membrane in sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Demonstration of an inactive enzyme antigen in sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Detection of primary and secondary sucrose malabsorption in children by means of the breath hydrogen technique.
sucrose alpha-glucosidase deficiency
Diagnostic value of sucrose tolerance test in children evaluated by breath hydrogen measurement.
sucrose alpha-glucosidase deficiency
Diet and intestinal enzyme adaptation: implications for gastrointestinal disorders.
sucrose alpha-glucosidase deficiency
Dietary fructose in the management of intractable diarrhea of infancy.
sucrose alpha-glucosidase deficiency
Dietary stimulation of sucrase in a patient with sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Differential Effects of Sucrase-Isomaltase Mutants on Its Trafficking and Function in Irritable Bowel Syndrome: Similarities to Congenital Sucrase-Isomaltase Deficiency.
sucrose alpha-glucosidase deficiency
Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Ethnic differences in intestinal disaccharidase values in children in Finland.
sucrose alpha-glucosidase deficiency
Evaluation of liquid yeast-derived sucrase enzyme replacement in patients with sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Failure of the hydrogen breath test to detect pulmonary sugar malabsorption.
sucrose alpha-glucosidase deficiency
Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome.
sucrose alpha-glucosidase deficiency
Glucose polymer as a cause of protracted diarrhea in infants with unsuspected congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Heterozygotes Are a Potential New Entity among Homozygotes and Compound Heterozygotes in Congenital Sucrase-Isomaltase Deficiency.
sucrose alpha-glucosidase deficiency
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2.
sucrose alpha-glucosidase deficiency
Hypomorphic SI genetic variants are associated with childhood chronic loose stools.
sucrose alpha-glucosidase deficiency
Improved Starch Digestion of Sucrase Deficient Shrews Treated with Oral Glucoamylase Enzyme Supplements.
sucrose alpha-glucosidase deficiency
Index of suspicion. Case 3. Congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Interaction of antipsychotic drugs with sucrase; kinetics and structural study.
sucrose alpha-glucosidase deficiency
Interaction of methocarbamol and yeast sucrase induces enzyme inhibition.
sucrose alpha-glucosidase deficiency
Intestinal disaccharidase activities in relation to age, race, and mucosal damage.
sucrose alpha-glucosidase deficiency
Intestinal sucrase and isomaltase deficiency in two siblings.
sucrose alpha-glucosidase deficiency
Intestinal sucrase deficiency presenting as sucrose intolerance in adult life.
sucrose alpha-glucosidase deficiency
Intestinal sucrase-isomaltase deficiency and renal calculi.
sucrose alpha-glucosidase deficiency
Letter: Gene frequency of sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Maltase-glucoamylase and residual isomaltase in sucrose intolerant patients.
sucrose alpha-glucosidase deficiency
Molecular basis of aberrant apical protein transport in an intestinal enzyme disorder.
sucrose alpha-glucosidase deficiency
Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients.
sucrose alpha-glucosidase deficiency
Mosaic pattern of sucrase isomaltase deficiency in two brothers.
sucrose alpha-glucosidase deficiency
Naturally occurring mutations in intestinal sucrase-isomaltase provide evidence for the existence of an intracellular sorting signal in the isomaltase subunit.
sucrose alpha-glucosidase deficiency
Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption.
sucrose alpha-glucosidase deficiency
Onset of sucrase-isomaltase deficiency in late adulthood.
sucrose alpha-glucosidase deficiency
Persistent diarrhea due to sucrase-isomaltase deficiency in a postoperative child with Hirschsprung's disease.
sucrose alpha-glucosidase deficiency
Primary combined saccharase and isomaltase deficiency. Report of two adult siblings of consanguineous parentage.
sucrose alpha-glucosidase deficiency
Primary sucrase-isomaltase deficiency: importance of clinical judgment.
sucrose alpha-glucosidase deficiency
Protracted diarrhoea in infancy. Analysis of 82 cases with particular reference to diagnosis and management.
sucrose alpha-glucosidase deficiency
Ranitidine induces inhibition and structural changes in sucrase.
sucrose alpha-glucosidase deficiency
Relationships among Dietary Intakes and Persistent Gastrointestinal Symptoms in Patients Receiving Enzyme Treatment for Genetic Sucrase-Isomaltase Deficiency.
sucrose alpha-glucosidase deficiency
Research progress reported at the 50th Anniversary of the Discovery of Congenital Sucrase-Isomaltase Deficiency Workshop.
sucrose alpha-glucosidase deficiency
Sacrosidase therapy for congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Starch digestion and patients with congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Subcellular fractionation studies of the intestinal mucosa in congenital sucrase--isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Sucrase-Isomaltase Deficiency as a Potential Masquerader in Irritable Bowel Syndrome.
sucrose alpha-glucosidase deficiency
Sucrase-Isomaltase Deficiency Causing Persistent Bloating and Diarrhea in an Adult Female.
sucrose alpha-glucosidase deficiency
Sucrase-isomaltase deficiency in humans. Different mutations disrupt intracellular transport, processing, and function of an intestinal brush border enzyme.
sucrose alpha-glucosidase deficiency
Sucrase-isomaltase deficiency. Absence of an inactive enzyme variant.
sucrose alpha-glucosidase deficiency
Sucrase-isomaltase deficiency: changing pattern over two decades.
sucrose alpha-glucosidase deficiency
Sucrase-isomaltase deficiency: difficulties in diagnosis.
sucrose alpha-glucosidase deficiency
Sucrase-Isomaltase Gene Variants in Patients with Abnormal Sucrase Activity and Functional GI Disorders.
sucrose alpha-glucosidase deficiency
Sucrose malabsorption in children: noninvasive diagnosis by interval breath hydrogen determination.
sucrose alpha-glucosidase deficiency
The brush border membrane in hereditary sucrase-isomaltase deficiency: abnormal protein pattern and presence of immunoreactive enzyme.
sucrose alpha-glucosidase deficiency
The clinical consequences of sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
The glucose-regulated protein GRP94 interacts avidly in the endoplasmic reticulum with sucrase-isomaltase isoforms that are associated with congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
The multiple roles of sucrase-isomaltase in the intestinal physiology.
sucrose alpha-glucosidase deficiency
The patient journey to diagnosis and treatment of congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
The Role of Disaccharidase Deficiencies in Functional Abdominal Pain Disorders-A Narrative Review.
sucrose alpha-glucosidase deficiency
Transport to cell surface of intestinal sucrase-isomaltase is blocked in the Golgi apparatus in a patient with congenital sucrase-isomaltase deficiency.
sucrose alpha-glucosidase deficiency
Uncommon causes of postoperative chronic diarrhoea mimicking enterocolitis in Hirschsprung's disease: is there a role for digestive endoscopy?
sucrose alpha-glucosidase deficiency
Value of breath hydrogen analysis in management of diarrheal illness in childhood: comparison with duodenal biopsy.
sucrose alpha-glucosidase deficiency
[Congenital primary saccharase and isomaltase deficiency of the small intestine]
sucrose alpha-glucosidase deficiency
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
sucrose alpha-glucosidase deficiency
[Congenital sucrase-isomaltase deficiency: a rare cause of chronic or recurrent diarrhea in children]
sucrose alpha-glucosidase deficiency
[Intestinal disaccharidase and alkaline phosphatase activities of jejunal biopsies in small bowel diseases of children (author's transl)]
sucrose alpha-glucosidase deficiency
[Peripheral gangrene in a congenital sucrase isomaltase deficiency (author's transl)]
sucrose alpha-glucosidase deficiency
[Primary saccharose-isomaltose deficit: a 20-year case load]
sucrose alpha-glucosidase deficiency
[Sucrase-isomaltase deficiency as a cause of chronic diarrhoea in adults (author's transl)]
sucrose alpha-glucosidase deficiency
[Sucrase-isomaltase deficiency. Value of the hydrogen respiratory test]
sucrose alpha-glucosidase deficiency
[Useful and superfluous measures in the treatment of infant diarrhea]
Vesicular Stomatitis
A novel type of detergent-resistant membranes may contribute to an early protein sorting event in epithelial cells.
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