Literature DB >> 7471478

Prenatal detection of defects in propionate metabolism.

U Wendel.   

Abstract

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Year:  1980        PMID： 7471478     DOI： 10.1016/0009-8981(80)90356-3

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN： 0009-8981            Impact factor:   3.786


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  2 in total

1.  Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. I. Clinical, metabolical, and biochemical findings.

Authors:  W Lehnert; U Wendel; S Lindenmaier; N Böhm
Journal:  Eur J Pediatr       Date:  1982-09       Impact factor: 3.183

2.  Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients.

Authors:  B A Amendt; C Greene; L Sweetman; J Cloherty; V Shih; A Moon; L Teel; W J Rhead
Journal:  J Clin Invest       Date:  1987-05       Impact factor: 14.808
  2 in total

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