Fuel utilization in patients with very long-chain acyl-coa dehydrogenase deficiency-Reference-Cited by-同舟云学术

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Fuel utilization in patients with very long-chain acyl-coa dehydrogenase deficiency

Published:2004-07-29 Issue:2 Volume:56 Page:279-283
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

ØRngreen Mette C.,Nørgaard Mette G.,Sacchetti Massimo,Van Engelen Baziel G. M.,Vissing John

Funder

Danish National Research Foundation

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference20 articles.

1. Novel Fatty acid beta-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase;Izai;J Biol Chem,1992

2. Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients;Saban;Clin Chim Acta,1998

3. Very long-chain acyl coenzyme A dehydrogenase deficiency presenting with exercise-induced myoglobinuria;Ogilvie;Neurology,1994

4. Recurrent myoglobinuria as a presenting manifestation of very long chain acyl coenzyme A dehydrogenase deficiency;Straussberg;Pediatrics,1998

5. Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria;Minetti;Neuromuscul Disord,1998

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2. No effect of resveratrol on fatty acid oxidation or exercise capacity in patients with fatty acid oxidation disorders: A randomized clinical cross‐over trial;Journal of Inherited Metabolic Disease;2022-02-04

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4. Mitochondrial morphology, bioenergetics and proteomic responses in fatty acid oxidation disorders;Redox Biology;2021-05

5. Nutrition management guideline for very-long chain acyl-CoA dehydrogenase deficiency (VLCAD): An evidence- and consensus-based approach;Molecular Genetics and Metabolism;2020-09

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