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Ethylmalonic aciduria: an organic acidemia with CNS involvement and vasculopathy

  • Published:1994-11 Issue: Volume:16 Page:12-22
  • ISSN:0387-7604
  • Container-title:Brain and Development
  • language:en
  • Short-container-title:Brain and Development

Author:

Ozand P.T.,Rashed M.,Millington D.S.,Sakati N.,Hazzaa S.,Rahbeeni Z.,Al Odaib A.,Youssef N.,Mazrou A.,Gascon G.G.,Brismar J.

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference13 articles.

1. The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defect;Bennett;J Inherit Metab Dis,1985

2. Short-chain-acyl-Coenzyme A dehydrogenase deficiency;Amendt;J Clin Invest,1987

3. Short-chain Acyl-CoA dehydrogenase deficiency;Turnbull;Prog Clin Biol Res,1989

4. Fatty acid oxidation disorders: a new class of metabolic diseases;Hale;J Pediatr,1992

5. Inborn errors of fatty acid oxidation in man;Rhead;Clin Biochem,1991

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