Ethylmalonic Aciduria Is Associated with an Amino Acid Variant of Short Chain Acyl-Coenzyme A Dehydrogenase-Reference-Cited by-同舟云学术

Ethylmalonic Aciduria Is Associated with an Amino Acid Variant of Short Chain Acyl-Coenzyme A Dehydrogenase

Published:1996-06 Issue:6 Volume:39 Page:1059-1066
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Corydon M J,Gregersen N,Lehnert W,Ribes A,Rinaldo P,Kmoch S,Christensen E,Kristensen T J,Andresen B S,Bross P,Winter V,Martinez G,Neve S,Jensen T G,Bolund L,Kølvraa S

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference47 articles.

1. THE ENZYMATIC CARBOXYLATION OF BUTYRYL COENZYME A

2. Clinical and Biochemical Variation and Family Studies in the Multiple Acyl-CoA Dehydrogenation Disorders

3. Glutaric acidaemia type II (multiple Acyl-Coa dehydrogenation deficiency)

4. Ethylmalonic/Adipic Aciduria: Effects of Oral Medium-Chain Triglycerides, Carnitine, and Glycine on Urinary Excretion of Organic Acids, Acylcarnitines, and Acylglycines

5. C6—C10-Dicarboxylic Aciduria: Investigations of a Patient with Riboflavin Responsive Multiple Acyl-CoA Dehydrogenation Defects

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