Literature DB >> 7923814

The enzymes of mitochondrial fatty acid oxidation.

M J Bennett1.   

Abstract

Defects of mitochondrial fatty acid oxidation are recent additions to the catalogue of inherited metabolic diseases. This review focuses upon decent developments in our understanding of the basic biochemistry, clinical presentations and molecular genetics of fatty acid oxidation disorders, with an emphasis on the strategies being used to define new disorders.

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Year:  1994        PMID： 7923814     DOI： 10.1016/0009-8981(94)90216-x

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


  2 in total

1.  Medium-chain acyl-CoA dehydrogenase deficiency presenting in the neonatal period: the first Italian case.

Authors:  A B Burlina; M J Bennett; N Gregersen; B Dalla Barba; F Zacchello
Journal:  Eur J Pediatr       Date:  1995-11       Impact factor: 3.183

2.  Medium chain acylcarnitines dominate the metabolite pattern in humans under moderate intensity exercise and support lipid oxidation.

Authors:  Rainer Lehmann; Xinjie Zhao; Cora Weigert; Perikles Simon; Elvira Fehrenbach; Jens Fritsche; Jürgen Machann; Fritz Schick; Jiangshan Wang; Miriam Hoene; Erwin D Schleicher; Hans-Ulrich Häring; Guowang Xu; Andreas M Niess
Journal:  PLoS One       Date:  2010-07-12       Impact factor: 3.240
  2 in total

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