Literature DB >> 1527994

Fatal outcome in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

A Ribes1, E Riudor, C Navarro, M Boronat, M Marti, D E Hale.   

Abstract

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Year:  1992        PMID： 1527994     DOI： 10.1007/bf01799642

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


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  2 in total

1.  3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment.

Authors:  M Duran; R J Wanders; J P de Jager; L Dorland; L Bruinvis; D Ketting; L Ijlst; F J van Sprang
Journal:  Eur J Pediatr       Date:  1991-01       Impact factor: 3.183

2.  Prophylaxis of early ventricular fibrillation by inhibition of acylcarnitine accumulation.

Authors:  P B Corr; M H Creer; K A Yamada; J E Saffitz; B E Sobel
Journal:  J Clin Invest       Date:  1989-03       Impact factor: 14.808
  2 in total
  2 in total

Review 1.  Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a severe fatty acid oxidation disorder.

Authors:  A C Sewell; S W Bender; S Wirth; H Münterfering; L Ijlist; R J Wanders
Journal:  Eur J Pediatr       Date:  1994-10       Impact factor: 3.183

Review 2.  Mitochondrial dysfunction in fatty acid oxidation disorders: insights from human and animal studies.

Authors:  Moacir Wajner; Alexandre Umpierrez Amaral
Journal:  Biosci Rep       Date:  2015-11-20       Impact factor: 3.840
  2 in total

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