His primary areas of study are Internal medicine, Endocrinology, Biochemistry, Acyl CoA dehydrogenase and Dehydrogenase. The Internal medicine study combines topics in areas such as Diabetes mellitus and Genetics, Newborn screening. The study incorporates disciplines such as Cardiomyopathy and Myopathy in addition to Endocrinology.
His research investigates the connection between Biochemistry and topics such as Stereochemistry that intersect with issues in Plasma protein binding, Substrate, Protein folding and Ligand. His Acyl CoA dehydrogenase research includes themes of Beta oxidation, Molecular cloning and Nucleic acid sequence. His Dehydrogenase research includes elements of Oxidoreductase and Leucine.
His scientific interests lie mostly in Internal medicine, Biochemistry, Endocrinology, Acyl CoA dehydrogenase and Dehydrogenase. His Internal medicine research is multidisciplinary, relying on both Gastroenterology and Newborn screening. His study looks at the relationship between Biochemistry and topics such as Molecular biology, which overlap with Gene.
In the field of Endocrinology, his study on Hypoglycemia overlaps with subjects such as Coenzyme A. His Acyl CoA dehydrogenase research incorporates themes from Mutation and Fatty acid, Fatty acid metabolism. His research investigates the connection with Dehydrogenase and areas like Stereochemistry which intersect with concerns in Flavin group.
His primary areas of study are Internal medicine, Endocrinology, Beta oxidation, Mitochondrion and Adverse effect. His Internal medicine research focuses on Gastroenterology and how it relates to Phenylalanine hydroxylase. Jerry Vockley has included themes like Ataxia, Muscle weakness, ACADS and Ubiquinone Deficiency in his Endocrinology study.
His work carried out in the field of Beta oxidation brings together such families of science as Long chain fatty acid, Carnitine, Newborn screening and Asymptomatic. His research integrates issues of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Electron transport chain in his study of Mitochondrion. Acyl CoA dehydrogenase is the subject of his research, which falls under Biochemistry.
Internal medicine, Mitochondrion, Adverse effect, Phenylalanine hydroxylase and Disease are his primary areas of study. His studies in Internal medicine integrate themes in fields like Gastroenterology and Endocrinology. His Endocrinology research incorporates elements of Exome sequencing, Mutation, Old Order Amish and Myeloid.
Cell biology and Biochemistry are the subject areas of his Mitochondrion study. His studies deal with areas such as Clinical trial, Randomized controlled trial, Mitochondrial myopathy and Dose–response relationship as well as Adverse effect. His study in Disease is interdisciplinary in nature, drawing from both Multivariate analysis, Metabolic disease, Liver disease, Living donor liver transplantation and Transplantation.
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Effects of Diet and Physical Activity Interventions on Weight Loss and Cardiometabolic Risk Factors in Severely Obese Adults: A Randomized Trial
Bret H. Goodpaster;James P. DeLany;Amy D. Otto;Lewis Kuller.
Increased levels of plasma acylcarnitines in obesity and type 2 diabetes and identification of a marker of glucolipotoxicity.
Stephanie J. Mihalik;Bret H. Goodpaster;David E. Kelley;Donald H. Chace.
Phenylalanine hydroxylase deficiency: diagnosis and management guideline.
Jerry Vockley;Hans C. Andersson;Kevin M. Antshel;Nancy E. Braverman.
Genetics in Medicine (2014)
Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathways.
Jerry Vockley;Piero Rinaldo;Michael J. Bennett;Dietrich Matern.
Molecular Genetics and Metabolism (2000)
Phenylketonuria Scientific Review Conference: state of the science and future research needs.
Kathryn M. Camp;Melissa A. Parisi;Phyllis B. Acosta;Gerard T. Berry.
Molecular Genetics and Metabolism (2014)
Metabolomic Profiling of Fatty Acid and Amino Acid Metabolism in Youth With Obesity and Type 2 Diabetes: Evidence for enhanced mitochondrial oxidation
Stephanie J. Mihalik;Sara F. Michaliszyn;Javier de las Heras;Fida Bacha.
Diabetes Care (2012)
Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation
D. M. Kurtz;P. Rinaldo;W. J. Rhead;Liqun Tian.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Molecular cloning and nucleotide sequence of cDNAs encoding the precursors of rat long chain acyl-coenzyme A, short chain acyl-coenzyme A, and isovaleryl-coenzyme A dehydrogenases. Sequence homology of four enzymes of the acyl-CoA dehydrogenase family.
Y Matsubara;Y Indo;E Naito;H Ozasa.
Journal of Biological Chemistry (1989)
Molecular Heterogeneity in Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency Causing Pediatric Cardiomyopathy and Sudden Death
Amit Mathur;Harold F. Sims;Deepika Gopalakrishnan;Beverly Gibson.
Efficacy of sapropterin dihydrochloride in increasing phenylalanine tolerance in children with phenylketonuria: a phase III, randomized, double-blind, placebo-controlled study.
Friedrich K. Trefz;Barbara K. Burton;Nicola Longo;Mercedes Martinez Pardo Casanova.
The Journal of Pediatrics (2009)
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