Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake-Reference-Cited by-同舟云学术

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

Published:1991-11 Issue:5 Volume:30 Page:709-716
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Stanley Charles A.,DeLeeuw Susan,Coates Paul M.,Vianey-Liaud Christine,Divry Priscille,Bonnefont Jean-Paul,Saudubray Jean-Marie,Haymond Morey,Trefz Friedrich K.,Breningstall Galen N.,Wappner Rebecca S.,Byrd Dennis J.,Sansaricq Claude,Tein Ingrid,Grover Warren,Valle David,Rutledge S. Lane,Treem William R.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference23 articles.

1. Carnitine--metabolism and functions

2. Comparative aspects of carnitine biosynthesis in microorganisms and mammals with attention to carnitine biosynthesis in man. In: eds. Carnitine biosynthesis, metabolism and functions. New York: Academic Press, 1989: 57-67.

3. Primary Carnitine Deficiency Due to a Failure of Carnitine Transport in Kidney, Muscle, and Fibroblasts

4. Hereditary defect in carnitine membrane transport is expressed in skin fibroblasts

5. Transport of carnitine into cells in hereditary carnitine deficiency

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