Heterozygotes for plasmalemmal carnitine transporter defect are at increased risk for valproic acid-associated impairment of carnitine uptake in cultured human skin fibroblasts-Reference-Cited by-同舟云学术

Heterozygotes for plasmalemmal carnitine transporter defect are at increased risk for valproic acid-associated impairment of carnitine uptake in cultured human skin fibroblasts

Published:1995-05 Issue:3 Volume:18 Page:313-322
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Tein I.,DiMauro S.,Xie Z. -W.,De Vivo D. C.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00710422

Reference33 articles.

1. Addison GM, Gordon NS (1980) Sodium valproate and acute hepatic failure.Dev Med Child Neurol 22: 248?249.

2. Ater SB, Swinyard EA, Tolman KG, Madsen JA, Matsuo F (1984) Effects of SKF525A, phenobarbital, fasting, and carnitine on the anticonvulsant activity and neurotoxicity of valproate in mice.Epilepsia 25: 599?604.

3. Beghi E, Bizzi A, Codegoni AM, Trevisan D, Torri W (1990) Valproate, carnitine metabolism and biochemical indicators of liver function. Collaborative Group for the Study of Epilepsy.Epilepsia 31: 346?352.

4. Bohles H, Richter K, Wagner-Thiessen E, Schafer H (1982) Decreased serum carnitine in valproate-induced Reye syndrome.Eur J Pediatr 139: 185?186.

5. Coulter DL (1984) Carnitine deficiency: A possible mechanism for valproate hepatotoxicity [letter].Lancet 1: 689.

Cited by 10 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. Pathophysiology of fatty acid oxidation disorders and resultant phenotypic variability;Journal of Inherited Metabolic Disease;2013-05-15

2. Serum Carnitine Levels During Oxcarbazepine and Carbamazepine Monotherapies in Children With Epilepsy;Journal of Child Neurology;2003-08

3. Expression and localization of organic cation/carnitine transporter OCTN2 in Caco-2 cells;American Journal of Physiology-Gastrointestinal and Liver Physiology;2003-05-01

4. Overview of inherited metabolic disorders causing cardiovascular disease;Journal of Inherited Metabolic Disease;2003-03

5. Carnitine transport: Pathophysiology and metabolism of known molecular defects;Journal of Inherited Metabolic Disease;2003-03