Physician
Medical Genetics
Dr. Charles R. Roe, MD
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Dr. Charles R. Roe practices Medical Genetics. He went to medical school at Duke University School of Medicine. Duke University School of Medicine is a one of the best medicals schools. Duke University School of Medicine is ranked 8/29 in Research/PrimaryCare. Dr. Charles R. Roe is a published doctor and has 22 publications published. The lastest was: 'Anaplerotic treatment of long-chain fat oxidation disorders with triheptanoin: Review of 15years Experience.'
Publications
- Anaplerotic treatment of long-chain fat oxidation disorders with triheptanoin: Review of 15years Experience.
- Triheptanoin for Glucose Transporter Type I Deficiency (G1D): Modulation of Human Ictogenesis, Cerebral Metabolic Rate, and Cognitive Indices by a Food Supplement.
- Adult Polyglucosan Body Disease (APBD): Anaplerotic diet therapy (Triheptanoin) and demonstration of defective methylation pathways.
- Pyruvate carboxylase deficiency: mechanisms, mimics and anaplerosis.
- Effect of dietary fats with odd or even numbers of carbon atoms on metabolic response and muscle damage with exercise in Quarter Horse-type horses with type 1 polysacc...
- Parenteral and enteral metabolism of anaplerotic triheptanoin in normal rats. II. Effects on lipolysis, glucose production, and liver acyl-CoA profile.
- Interrelations between C4 ketogenesis, C5 ketogenesis, and anaplerosis in the perfused rat liver.
- Effect of triheptanoin on muscle metabolism during submaximal exercise in horses.
- Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewis...
- Choice of oils for essential fat supplements can enhance production of abnormal metabolites in fat oxidation disorders.
- REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish popul...
- Parenteral and enteral metabolism of anaplerotic triheptanoin in normal rats.
- Variations in IBD (ACAD8) in children with elevated C4-carnitine detected by tandem mass spectrometry newborn screening.
- Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapy.
- Clinical effects of L-carnitine supplementation on apnea and growth in very low birth weight infants.
- Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans.
- Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride.
- Assay of the concentration and (13)C isotopic enrichment of propionyl-CoA, methylmalonyl-CoA, and succinyl-CoA by gas chromatography-mass spectrometry.
- Inherited disorders of mitochondrial fatty acid oxidation: a new responsibility for the neonatologist.
- Anaplerotic diet therapy in inherited metabolic disease: therapeutic potential.
- Anaplerotic molecules: current and future.
Schools
Duke University
Duke University Med Center
Doctors Specialties
- Other
- Pediatrics
- Medical Genetics
Accepted Insurances
Education
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Duke University Hospital -
Duke University School of Medicine
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