Clinical and Biochemical Variation and Family Studies in the Multiple Acyl-CoA Dehydrogenation Disorders-Reference-Cited by-同舟云学术

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

Published:1987-04 Issue:4 Volume:21 Page:371-376
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Rhead William J,Wolff Jon A,Lipson Mark,Falace Peggy,Desai Nirmala,Fritchman Kathie,Moon Anne,Sweetman Lawrence

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Cited by 40 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Biomarkers for mitochondrial energy metabolism diseases;Essays in Biochemistry;2018-07-06

2. Disorders of vitamins and cofactors;Biomarkers in Inborn Errors of Metabolism;2017

3. Successful Pregnancy in a Young Woman with Multiple Acyl-CoA Dehydrogenase Deficiency;JIMD Reports;2017

4. Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin;Journal of Pediatric Endocrinology and Metabolism;2016-01-01

5. Inhibition of N-acetylglutamate synthase by various monocarboxylic and dicarboxylic short-chain coenzyme A esters and the production of alternative glutamate esters;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2014-12

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