Renal Handling of Carnitine in Secondary Carnitine Deficiency Disorders-Reference-Cited by-同舟云学术

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Renal Handling of Carnitine in Secondary Carnitine Deficiency Disorders

Published:1993-07 Issue:1 Volume:34 Page:89-96
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Stanley Charles A,Berry Gerard T,Bennett Michael J,Willi Steven M,Treem William R,Hale Daniel E

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Cited by 37 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. Pathophysiological mechanisms of complications associated with propionic acidemia;Pharmacology & Therapeutics;2023-09

2. Plasma carnitine concentrations in Medium‐chain acyl‐CoA dehydrogenase deficiency: lessons from an observational cohort study;Journal of Inherited Metabolic Disease;2022-07-17

3. Biochemical assays of TCA cycle and β-oxidation metabolites;Methods in Cell Biology;2020

4. Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California;Molecular Genetics and Metabolism;2017-11

5. Disorders of Branched Chain Amino Acid Metabolism;2017

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