Isovaleric acidemia: Identification of isovalerate, isovalerylglycine, and 3-hydroxyisovalerate in urine of a patient previously reported as having butyric and hexanoic acidemia-Reference-Cited by-同舟云学术

Isovaleric acidemia: Identification of isovalerate, isovalerylglycine, and 3-hydroxyisovalerate in urine of a patient previously reported as having butyric and hexanoic acidemia

Published:1973-02 Issue:2 Volume:82 Page:243-248
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Ando Toshiyuki,Nyhan William L.,Bachmann Claude,Rasmussen Karsten,Scott Ronald,Smith Elizabeth K.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference13 articles.

1. Isovaleric acidemia: A new genetic defect of leucine metabolism;Tanaka;Proc. Natl. Acad. Sci. U. S. A.,1966

2. An inborn error of short-chain fatty acid metabolism;Sidbury;J. Pediatr.,1967

3. Neonatal death associated with isovaleric acidemia;Newman;Lancet,1967

4. The isolation and identification of N-isovalerylglycine from urine of patients with isovaleric acidemia;Tanaka;J. Biol. Chem.,1967

5. Isovaleric acidemia presenting with altered metabolism of glycine;Ando;Pediatr. Res.,1971

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