3-Hydroxyisobutyric Aciduria in Two Brothers-Reference-Cited by-同舟云学术

3-Hydroxyisobutyric Aciduria in Two Brothers

Published:1998-03 Issue:3 Volume:18 Page:253-255
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Sasaki Masayuki,Kimura Masahiko,Sugai Kenji,Hashimoto Toshiaki,Yamaguchi Seiji

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference10 articles.

1. Branched chain organic acidurias;Sweetman,1995

2. 3-Hydroxyisobutyric aciduria with a mild clinical course;Boulat;J Inherit Metab Dis,1995

3. 3-Hydroxyisobutyric aciduria;Ko;Pediatr Res,1991

4. Mienie LJ, Erasmus E. Biochemical studies on a patient with a possible 3-hydroxyisobutyrate dehydrogenase deficiency. Proceedings of the Fifth International Congress of Inborn Errors of Metabolism; 1990 June 1-5; Pacific Grove, CA. Pacific Grove, CA: Society for Inherited Metabolic Disorders, 1990.

5. Valine-related 3-hydroxyisobutyric aciduria in twins;Brewster;Proc Soc Inherit Metab Dis,1991

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