Recurrent Myoglobinuria as a Presenting Manifestation of Very Long Chain Acyl Coenzyme A Dehydrogenase Deficiency-Reference-Cited by-同舟云学术

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Recurrent Myoglobinuria as a Presenting Manifestation of Very Long Chain Acyl Coenzyme A Dehydrogenase Deficiency

Published:1997-06-01 Issue:6 Volume:99 Page:894-896
ISSN:1098-4275
Container-title:Pediatrics
language:en
Short-container-title:

Author:

Straussberg Rachel,Harel Liora,Varsano Izhak,Elpeleg Orly N.,Shamir Ra'anan,Amir Jacob

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

Link

https://publications.aap.org/pediatrics/article-pdf/99/6/894/999128/e2.pdf

Reference16 articles.

1. Hypoglycemia, hypotonia and cardiomyopathy: the evolving clinical picture of long chain acyl-coA dehydrogenase deficiency.;Treem;Pediatrics.,1991

2. Fatty acid oxidation disorders: a new class of metabolic diseases.;Hale;J Pediatr.,1992

3. 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

4. Disorders of mitochondrial long-chain fatty acid oxidation.;Pollitt;J Inherit Metab Dis.,1995

5. Mitochondrial very long chain acyl-coA dehydrogenase deficiency–a new disorder of fatty acid oxidation.;Largilliere;Arch Dis Child.,1995

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

2. Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations;The American Journal of Human Genetics;2016-02

3. Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency;Molecular Genetics and Metabolism Reports;2015-06

4. Lipid Storage Myopathies Due to Fatty Acid Oxidation Defects;Neuromuscular Disorders of Infancy, Childhood, and Adolescence;2015

5. Intolérance musculaire à l'effort;EMC - Neurologie;2010-01

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