L-Carnitine in inborn errors of metabolism: What is the evidence?-Reference-Cited by-同舟云学术

L-Carnitine in inborn errors of metabolism: What is the evidence?

Published:2003-03 Issue:2-3 Volume:26 Page:181-188
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Walter J. H.¹

Affiliation:

1. ; Willink Biochemical Genetics Unit; Royal Manchester Children's Hospital; Manchester M27 4HA UK

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1024485117095/fullpdf

Reference21 articles.

1. Isovaleric acidemia: medical and neurodevelopmental effects of long-term therapy;Berry;J Pediatr,1988

2. Urinary excretion of L-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of L-carnitine;Chalmers;Pediatr Res,1984

3. L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria;Chalmers;J Inherit Metab Dis,1984

4. The response to L-carnitine and glycine therapy in isovaleric acidaemia;De Sousa;Eur J Pediatr,1986

5. Direct identification of propionylcarnitine in propionic acidaemia: biochemical and clinical results of oral carnitine supplementation;Duran;J Inherit Metab Dis,1986

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