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Anita MacDonald, Rachel Webster, Matthew Whitlock, Adam Gerrard, Anne Daly, Mary Anne Preece, Sharon Evans, Catherine Ashmore, Anupam Chakrapani, Suresh Vijay, Saikat Santra

Journal of pediatric endocrinology & metabolism : JPEM 2018;31(3):297-304

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Effects of intermittent hypoxic training on amino and fatty acid oxidative combustion in human permeabilized muscle fibers.

Belle Roels, Claire Thomas, David J Bentley, Jacques Mercier, Maurice Hayot, Grégoire Millet

Journal of applied physiology (Bethesda, Md. : 1985) 2007;102(1):79-86

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Twice-a-day training improves mitochondrial efficiency, but not mitochondrial biogenesis, compared with once-daily training.

Yves Tourneur, Thaysa Ghiarone, Victor A Andrade-Souza, Sara K Learsi, Fabiano Tomazini, Thays Ataide-Silva, Andre Sansonio, Mariana P Fernandes, Karina L Saraiva, Regina C B Q Figueiredo, Jujiao Kuang, Adriano E Lima-Silva, David J Bishop

Journal of applied physiology (Bethesda, Md. : 1985) 2020;127(3):713-725

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Hyperinsulinism in infancy: understanding the pathophysiology.

A Aynsley-Green, K Hussain

The international journal of biochemistry & cell biology 2003;35(9):1312-7

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Effects of higher dietary protein intake on energy balance and metabolic control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency.

Melanie B Gillingham, Jonathan Q Purnell, Julia Jordan, Diane Stadler, Andrea M Haqq, Cary O Harding

Molecular genetics and metabolism 2007;90(1):64-9

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Results for ""3-Hydroxyacyl CoA Dehydrogenases""[mesh_terms]

Infantile Neurodegeneration Results from Mutants of 17β-Hydroxysteroid Dehydrogenase Type 10 Rather Than Aβ-Binding Alcohol Dehydrogenase.

Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl-coenzyme A dehydrogenase hyperinsulinism.

3-Hydroxyacyl-CoA and Alcohol Dehydrogenase Activities of Mitochondrial Type 10 17β-Hydroxysteroid Dehydrogenase in Neurodegeneration Study.

Novel insights into fatty acid oxidation, amino acid metabolism, and insulin secretion from studying patients with loss of function mutations in 3-hydroxyacyl-CoA dehydrogenase.

Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey.

Retinitis pigmentosa as a clinical presentation of LCHAD deficiency: A clinical case and review of the literature.

HSD10 disease: clinical consequences of mutations in the HSD17B10 gene.

Inborn errors of isoleucine degradation: a review.

HSD17B10: a gene involved in cognitive function through metabolism of isoleucine and neuroactive steroids.

Effect of L-carnitine supplementation and aerobic training on FABPc content and beta-HAD activity in human skeletal muscle.

The safety of Lipistart, a medium-chain triglyceride based formula, in the dietary treatment of long-chain fatty acid disorders: a phase I study.

Effects of intermittent hypoxic training on amino and fatty acid oxidative combustion in human permeabilized muscle fibers.

Twice-a-day training improves mitochondrial efficiency, but not mitochondrial biogenesis, compared with once-daily training.

Hyperinsulinism in infancy: understanding the pathophysiology.

Effects of higher dietary protein intake on energy balance and metabolic control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency.

Results for
""3-Hydroxyacyl CoA Dehydrogenases""[mesh_terms]