Literature DB >> 7623447

Decreased activity of respiratory-chain enzymes in glutaric aciduria type II.

R Santer1, A Claass, M Krawinkel, J Schaub, W Ruitenbeek.   

Abstract

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Year:  1995        PMID： 7623447     DOI： 10.1007/bf00711377

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  2 in total

1.  Assessment of deficiencies of fatty acyl-CoA dehydrogenases in fibroblasts, muscle and liver.

Authors:  H R Scholte; J D Ross; W Blom; A M Boonman; O P van Diggelen; C L Hall; J G Huijmans; I E Luyt-Houwen; W J Kleijer; J B de Klerk
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndrome.

Authors:  W R Treem; C A Witzleben; D A Piccoli; C A Stanley; D E Hale; P M Coates; J B Watkins
Journal:  Hepatology       Date:  1986 Nov-Dec       Impact factor: 17.425
  2 in total
  1 in total

1.  Novel ETF dehydrogenase mutations in a patient with mild glutaric aciduria type II and complex II-III deficiency in liver and muscle.

Authors:  Lynne A Wolfe; Miao He; Jerry Vockley; Nicole Payne; William Rhead; Charles Hoppel; Elaine Spector; Kim Gernert; K Michael Gibson
Journal:  J Inherit Metab Dis       Date:  2010-11-19       Impact factor: 4.982
  1 in total

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