5.4.99.2 Acidosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15647267&form=6&db=m Nitric oxide inhibits mammalian methylmalonyl-CoA mutase. causal interaction,unassigned 4,0 5.4.99.2 Acidosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26077484&form=6&db=m Early Liver Transplantation for Neonatal-Onset Methylmalonic Acidemia. causal interaction,unassigned 3,0 5.4.99.2 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2507694&form=6&db=m Vitamins and inherited human errors of metabolism. causal interaction,unassigned 2,0 5.4.99.2 Argininosuccinic Aciduria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26589311&form=6&db=m Inborn Errors of Metabolism in the United Arab Emirates: Disorders Detected by Newborn Screening (2011-2014). causal interaction,diagnostic usage,unassigned 2,3,0 5.4.99.2 Ataxia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8789622&form=6&db=m Effect of N2O treatment/vitamin B12 deficiency in pigs on tissue concentrations of odd-numbered, branched-chain fatty acids. diagnostic usage,ongoing research,unassigned 1,2,0 5.4.99.2 biotin-[propionyl-coa-carboxylase (atp-hydrolysing)] ligase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2507694&form=6&db=m Vitamins and inherited human errors of metabolism. causal interaction,unassigned 2,0 5.4.99.2 biotinidase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26589311&form=6&db=m Inborn Errors of Metabolism in the United Arab Emirates: Disorders Detected by Newborn Screening (2011-2014). causal interaction,causal interaction,diagnostic usage,diagnostic usage,unassigned,unassigned 2,2,3,3,0,0 5.4.99.2 Brain Ischemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8929440&form=6&db=m Methylmalonyl-CoA mutase induction by cerebral ischemia and neurotoxicity of the mitochondrial toxin methylmalonic acid. unassigned - 5.4.99.2 branched-chain-2-oxoacid decarboxylase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1016232&form=6&db=m Demonstration of a new mammalian isoleucine catabolic pathway yielding an Rseries of metabolites. causal interaction,unassigned 4,0 5.4.99.2 Coma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26077484&form=6&db=m Early Liver Transplantation for Neonatal-Onset Methylmalonic Acidemia. causal interaction,unassigned 3,0 5.4.99.2 Coma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27519416&form=6&db=m Novel Mouse Models of Methylmalonic Aciduria Recapitulate Phenotypic Traits with a Genetic Dosage Effect. unassigned - 5.4.99.2 Demyelinating Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1354465&form=6&db=m Cobalamin deficiency and the pathogenesis of nervous system disease. ongoing research,unassigned 2,0 5.4.99.2 Genetic Diseases, Inborn http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6885824&form=6&db=m Recognition, isolation, and characterization of rat liver D-methylmalonyl coenzyme A hydrolase. causal interaction,unassigned 3,0 5.4.99.2 Genetic Diseases, Inborn http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17957493&form=6&db=m Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group. causal interaction,unassigned 1,0 5.4.99.2 Glioma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7628092&form=6&db=m Fully automated assay for cobalamin-dependent methylmalonyl CoA mutase. diagnostic usage,ongoing research,unassigned 3,4,0 5.4.99.2 Glioma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9685364&form=6&db=m Disruption of a regulatory system involving cobalamin distribution and function in a methionine-dependent human glioma cell line. ongoing research,unassigned 3,0 5.4.99.2 Glioma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10377254&form=6&db=m Co-ordinate variations in methylmalonyl-CoA mutase and methionine synthase, and the cobalamin cofactors in human glioma cells during nitrous oxide exposure and the subsequent recovery phase. ongoing research,therapeutic application,unassigned 4,1,0 5.4.99.2 Holocarboxylase Synthetase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2507694&form=6&db=m Vitamins and inherited human errors of metabolism. causal interaction,unassigned 2,0 5.4.99.2 Homocystinuria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2507694&form=6&db=m Vitamins and inherited human errors of metabolism. causal interaction,unassigned 2,0 5.4.99.2 Homocystinuria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6511919&form=6&db=m Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis. unassigned - 5.4.99.2 Homocystinuria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9266389&form=6&db=m Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC). diagnostic usage,unassigned 3,0 5.4.99.2 Homocystinuria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10399092&form=6&db=m Progressive neurological deterioration and MRI changes in cblC methylmalonic acidaemia treated with hydroxocobalamin. causal interaction,unassigned 1,0 5.4.99.2 Homocystinuria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11237984&form=6&db=m Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findings. unassigned - 5.4.99.2 Hyperglycinemia, Nonketotic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17092&form=6&db=m Effect of valine on propionate metabolism in control and hyperglycinemic fibroblasts and in rat liver. diagnostic usage,ongoing research,unassigned 4,4,0 5.4.99.2 Hyperhomocysteinemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32186706&form=6&db=m The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphology. causal interaction,therapeutic application,unassigned 4,1,0 5.4.99.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21084167&form=6&db=m Host expression of methylmalonyl-CoA mutase and tuberculosis: a missing link? causal interaction,ongoing research,therapeutic application,unassigned 1,2,1,0 5.4.99.2 Kidney Failure, Chronic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23898205&form=6&db=m Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia. causal interaction,unassigned 1,0 5.4.99.2 Maple Syrup Urine Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2507694&form=6&db=m Vitamins and inherited human errors of metabolism. causal interaction,unassigned 2,0 5.4.99.2 Maple Syrup Urine Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15902548&form=6&db=m Breastfeeding experience in inborn errors of metabolism other than phenylketonuria. diagnostic usage,therapeutic application,unassigned 2,1,0 5.4.99.2 medium-chain acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26589311&form=6&db=m Inborn Errors of Metabolism in the United Arab Emirates: Disorders Detected by Newborn Screening (2011-2014). causal interaction,diagnostic usage,unassigned 2,3,0 5.4.99.2 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7833369&form=6&db=m Overexpression of human methylmalonyl CoA mutase in mice after in vivo gene transfer with asialoglycoprotein/polylysine/DNA complexes. causal interaction,unassigned 4,0 5.4.99.2 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15643616&form=6&db=m Molecular basis of methylmalonyl-CoA mutase apoenzyme defect in 40 European patients affected by mut(o) and mut- forms of methylmalonic acidemia: identification of 29 novel mutations in the MUT gene. causal interaction,unassigned 4,0 5.4.99.2 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16823967&form=6&db=m Quantitative analysis of mitochondrial protein expression in methylmalonic acidemia by two-dimensional difference gel electrophoresis. causal interaction,unassigned 2,0 5.4.99.2 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21748409&form=6&db=m Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management. causal interaction,unassigned 3,0 5.4.99.2 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23045948&form=6&db=m [Mutation analysis of the methylmalonyl-CoA mutase gene in ten Mexican patients with methylmalonic acidemia]. diagnostic usage,unassigned 3,0 5.4.99.2 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23580368&form=6&db=m Novel Deletion Mutation Identified in a Patient with Late-Onset Combined Methylmalonic Acidemia and Homocystinuria, cblC Type. causal interaction,therapeutic application,unassigned 4,1,0 5.4.99.2 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30712249&form=6&db=m Mutation analysis of genes related to methylmalonic acidemia: identification of eight novel mutations. causal interaction,unassigned 1,0 5.4.99.2 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31260114&form=6&db=m Liver neoplasms in methylmalonic aciduria: An emerging complication. causal interaction,unassigned 4,0 5.4.99.2 Metabolism, Inborn Errors http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2507694&form=6&db=m Vitamins and inherited human errors of metabolism. causal interaction,unassigned 2,0 5.4.99.2 Metabolism, Inborn Errors http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17597648&form=6&db=m Long-term outcome in methylmalonic acidurias is influenced by the underlying defect (mut0, mut-, cblA, cblB). unassigned - 5.4.99.2 Metabolism, Inborn Errors http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25205257&form=6&db=m Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia. causal interaction,unassigned 1,0 5.4.99.2 Metabolism, Inborn Errors http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26790480&form=6&db=m Neutralizing Antibodies Against Adeno-Associated Viral Capsids in Patients with mut Methylmalonic Acidemia. causal interaction,unassigned 3,0 5.4.99.2 Metabolism, Inborn Errors http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30022420&form=6&db=m Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort. causal interaction,unassigned 3,0 5.4.99.2 Metabolism, Inborn Errors http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30428564&form=6&db=m Label-Free Quantitative Proteomics in a Methylmalonyl-CoA Mutase-Silenced Neuroblastoma Cell Line. causal interaction,unassigned 2,0 5.4.99.2 Metabolism, Inborn Errors http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32443888&form=6&db=m A False-Positive Case of Methylmalonic Aciduria by Tandem Mass Spectrometry Newborn Screening Dependent on Maternal Malnutrition in Pregnancy. causal interaction,unassigned 2,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25314&form=6&db=m Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiency. causal interaction,unassigned 4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28187&form=6&db=m Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiency. causal interaction,unassigned 4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31423&form=6&db=m Methylmalonyl-CoA mutase deficiency associated with severe neonatal hyperammonemia: activity of urea cycle enzymes. causal interaction,unassigned 4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=116077&form=6&db=m Deranged isoleucine metabolism during ketotic attacks in patients with methylmalonic acidaemia. causal interaction,diagnostic usage,therapeutic application,unassigned 4,2,1,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1363156&form=6&db=m Correction of methylmalonyl-CoA mutase deficiency in Mut0 fibroblasts and constitution of gene expression in primary human hepatocytes by retroviral-mediated gene transfer. ongoing research,unassigned 4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1975493&form=6&db=m Perspectives on methylmalonic acidemia resulting from molecular cloning of methylmalonyl CoA mutase. causal interaction,unassigned 4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6108749&form=6&db=m [Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)] causal interaction,unassigned 4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6148691&form=6&db=m Benign methylmalonic aciduria. causal interaction,therapeutic application,unassigned 4,1,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9590044&form=6&db=m [Isolated methylmalonyl-CoA mutase deficiency] causal interaction,ongoing research,therapeutic application,unassigned 4,2,2,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9787093&form=6&db=m Methylmalonic semialdehyde dehydrogenase deficiency: psychomotor delay and methylmalonic aciduria without metabolic decompensation. causal interaction,unassigned 3,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9929975&form=6&db=m Molecular analysis of methylmalonyl-CoA mutase deficiency: identification of three missense mutations in mut0 patients. causal interaction,diagnostic usage,unassigned 4,2,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10518277&form=6&db=m Towards metabolic sink therapy for mut methylmalonic acidaemia: correction of methylmalonyl-CoA mutase deficiency in T lymphocytes from a mut methylmalonic acidaemia child by retroviral-mediated gene transfer. therapeutic application,unassigned 1,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15902548&form=6&db=m Breastfeeding experience in inborn errors of metabolism other than phenylketonuria. diagnostic usage,therapeutic application,unassigned 2,1,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16435223&form=6&db=m Mutational spectrum in ten Italian patients affected by methylmalonyl-CoA mutase deficiency. causal interaction,diagnostic usage,unassigned 3,2,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16750411&form=6&db=m Liver transplantation is not curative for methylmalonic acidopathy caused by methylmalonyl-CoA mutase deficiency. causal interaction,ongoing research,unassigned 4,1,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17432548&form=6&db=m [Diagnosis and treatment of methylmalonic aciduria: a case report] causal interaction,ongoing research,unassigned 3,1,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17470278&form=6&db=m Adenoviral-mediated correction of methylmalonyl-CoA mutase deficiency in murine fibroblasts and human hepatocytes. causal interaction,ongoing research,unassigned 2,4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17937813&form=6&db=m Metabolic phenotype of methylmalonic acidemia in mice and humans: the role of skeletal muscle. ongoing research,unassigned 2,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18940555&form=6&db=m Brain Damage by Mild Metabolic Derangements in Methylmalonic Acidemia. causal interaction,unassigned 4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19806564&form=6&db=m [Analysis of the MUT gene mutations in patients with methylmalonic acidemia.] diagnostic usage,ongoing research,unassigned 2,2,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20077088&form=6&db=m Quantitation of methylmalonic acid in serum or plasma using isotope dilution-selected ion gas chromatography-mass spectrometry. causal interaction,diagnostic usage,unassigned 4,4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26449400&form=6&db=m Molecular, biochemical, and structural analysis of a novel mutation in patients with methylmalonyl-CoA mutase deficiency. causal interaction,diagnostic usage,unassigned 4,2,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26483233&form=6&db=m [Acute brainstem encephalitis and myelitis in a girl with isolated methylmalonic aciduria due to MUT gene defect]. causal interaction,unassigned 4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26589311&form=6&db=m Inborn Errors of Metabolism in the United Arab Emirates: Disorders Detected by Newborn Screening (2011-2014). causal interaction,diagnostic usage,unassigned 2,3,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31260114&form=6&db=m Liver neoplasms in methylmalonic aciduria: An emerging complication. causal interaction,unassigned 4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31269850&form=6&db=m Optic neuropathy in classical methylmalonic acidemia. causal interaction,unassigned 4,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32080200&form=6&db=m Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency. causal interaction,ongoing research,unassigned 4,2,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32238804&form=6&db=m Author Correction: Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency. causal interaction,ongoing research,unassigned 4,2,0 5.4.99.2 methylmalonyl-coa mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32754920&form=6&db=m Delineating the clinical spectrum of isolated methylmalonic acidurias: cblA and mut. causal interaction,unassigned 3,0 5.4.99.2 Mitochondrial Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18676166&form=6&db=m Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria. causal interaction,ongoing research,unassigned 1,4,0 5.4.99.2 Mitochondrial Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32080200&form=6&db=m Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency. causal interaction,ongoing research,unassigned 4,2,0 5.4.99.2 Mitochondrial Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32238804&form=6&db=m Author Correction: Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency. causal interaction,ongoing research,unassigned 4,2,0 5.4.99.2 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2507694&form=6&db=m Vitamins and inherited human errors of metabolism. causal interaction,unassigned 2,0 5.4.99.2 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26589311&form=6&db=m Inborn Errors of Metabolism in the United Arab Emirates: Disorders Detected by Newborn Screening (2011-2014). causal interaction,diagnostic usage,unassigned 2,3,0 5.4.99.2 Neural Tube Defects http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14654360&form=6&db=m Polymorphisms within the vitamin B12 dependent methylmalonyl-coA mutase are not risk factors for neural tube defects. causal interaction,diagnostic usage,unassigned 4,1,0 5.4.99.2 ornithine carbamoyltransferase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15902548&form=6&db=m Breastfeeding experience in inborn errors of metabolism other than phenylketonuria. diagnostic usage,therapeutic application,unassigned 2,1,0 5.4.99.2 Ornithine Carbamoyltransferase Deficiency Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15902548&form=6&db=m Breastfeeding experience in inborn errors of metabolism other than phenylketonuria. diagnostic usage,therapeutic application,unassigned 2,1,0 5.4.99.2 Phenylketonurias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26589311&form=6&db=m Inborn Errors of Metabolism in the United Arab Emirates: Disorders Detected by Newborn Screening (2011-2014). causal interaction,diagnostic usage,unassigned 2,3,0 5.4.99.2 Propionic Acidemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17092&form=6&db=m Effect of valine on propionate metabolism in control and hyperglycinemic fibroblasts and in rat liver. diagnostic usage,ongoing research,unassigned 4,4,0 5.4.99.2 Propionic Acidemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12043367&form=6&db=m [Diagnosis and follow up of 23 children with organic acidurias] unassigned - 5.4.99.2 Propionic Acidemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25205257&form=6&db=m Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia. causal interaction,unassigned 1,0 5.4.99.2 Propionic Acidemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31449969&form=6&db=m Multi-omics studies in cellular models of methylmalonic acidemia and propionic acidemia reveal dysregulation of serine metabolism. causal interaction,unassigned 2,0 5.4.99.2 Propionic Acidemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31451751&form=6&db=m Assessment of methylcitrate and methylcitrate to citrate ratio in dried blood spots as biomarkers for inborn errors of propionate metabolism. causal interaction,unassigned 4,0 5.4.99.2 Renal Insufficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16750411&form=6&db=m Liver transplantation is not curative for methylmalonic acidopathy caused by methylmalonyl-CoA mutase deficiency. causal interaction,ongoing research,unassigned 4,1,0 5.4.99.2 Seizures http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12732252&form=6&db=m Creatine protects against the convulsive behavior and lactate production elicited by the intrastriatal injection of methylmalonate. causal interaction,therapeutic application,unassigned 4,1,0 5.4.99.2 Seizures http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16469366&form=6&db=m Effectiveness of creatine monohydrate on seizures and oxidative damage induced by methylmalonate. causal interaction,unassigned 4,0 5.4.99.2 Tuberculosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18375549&form=6&db=m Functional characterization of a vitamin B12-dependent methylmalonyl pathway in Mycobacterium tuberculosis: implications for propionate metabolism during growth on fatty acids. therapeutic application,unassigned 1,0 5.4.99.2 Tuberculosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21084167&form=6&db=m Host expression of methylmalonyl-CoA mutase and tuberculosis: a missing link? causal interaction,ongoing research,therapeutic application,unassigned 1,2,1,0 5.4.99.2 Tuberculosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22848869&form=6&db=m Progress in Oral Vaccination against Tuberculosis in Its Main Wildlife Reservoir in Iberia, the Eurasian Wild Boar. therapeutic application,unassigned 2,0 5.4.99.2 Tuberculosis, Bovine http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18454807&form=6&db=m Influence of methylmalonyl-CoA mutase alleles on resistance to bovine tuberculosis in the European wild boar (Sus scrofa). ongoing research,therapeutic application,unassigned 3,1,0 5.4.99.2 udp-galactopyranose mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1975493&form=6&db=m Perspectives on methylmalonic acidemia resulting from molecular cloning of methylmalonyl CoA mutase. causal interaction,unassigned 4,0 5.4.99.2 udp-galactopyranose mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6108749&form=6&db=m [Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)] causal interaction,unassigned 4,0 5.4.99.2 udp-galactopyranose mutase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26483233&form=6&db=m [Acute brainstem encephalitis and myelitis in a girl with isolated methylmalonic aciduria due to MUT gene defect]. causal interaction,unassigned 4,0 5.4.99.2 Vitamin B 12 Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=656065&form=6&db=m Possible interrelationship between vitamins E and b12 in the disturbance in methylmalonate metabolism in vitamin E deficiency. causal interaction,unassigned 4,0 5.4.99.2 Vitamin B 12 Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=5035057&form=6&db=m Leukocyte methylmalonyl-CoA mutase. I. Vitamin B 12 deficiency. unassigned - 5.4.99.2 Vitamin B 12 Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8698552&form=6&db=m Effects of low concentrations of dietary cobalt on rumen succinate concentration in sheep. unassigned - 5.4.99.2 Vitamin B 12 Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16464760&form=6&db=m Two newborns with nutritional vitamin B12 deficiency: Challenges in newborn screening for vitamin B12 deficiency. causal interaction,unassigned 2,0 5.4.99.2 Vitamin B 12 Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20077088&form=6&db=m Quantitation of methylmalonic acid in serum or plasma using isotope dilution-selected ion gas chromatography-mass spectrometry. causal interaction,diagnostic usage,unassigned 4,4,0 5.4.99.2 Vitamin E Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=656065&form=6&db=m Possible interrelationship between vitamins E and b12 in the disturbance in methylmalonate metabolism in vitamin E deficiency. causal interaction,unassigned 4,0