Glutaric acidemia type II: Clinical, biochemical, and morphologic considerations-Reference-Cited by-同舟云学术

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Glutaric acidemia type II: Clinical, biochemical, and morphologic considerations

Published:1982-06 Issue:6 Volume:100 Page:946-950
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Goodman Stephen I.,Stene Dan O.,McCabe Edward R.B.,Norenberg Michael D.,Shikes Robert H.,Stumpf David A.,Blackburn Glen K.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference16 articles.

1. Glutaric aciduria type II: Report on a previously undescribed metabolic disorder;Przyrembel;Clin Chim Acta,1976

2. Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein;Goodman;Pediatr Res,1980

3. Glutaric aciduria type II;Sweetman;J Pediatr,1980

4. Biochemical studies on a patient with defects in the metabolism of acyl-CoA and sarcosine; another possible case of glutaric aciduria type II;Gregersen;J Inherited Metab Dis,1980

5. Diagnosis of organic acidemias by gas chromatography-mass spectrometry;Goodman,1981

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