Literature DB >> 8803784

Neonatal presentation of medium-chain acyl-CoA dehydrogenase deficiency in two families.

J M Kirk1, I A Laing, N Smith, W S Uttley.   

Abstract

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Year:  1996        PMID： 8803784     DOI： 10.1007/bf01799271

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


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  3 in total

1.  Neonatal symptoms in medium chain acyl coenzyme A dehydrogenase deficiency.

Authors:  B Wilcken; K H Carpenter; J Hammond
Journal:  Arch Dis Child       Date:  1993-09       Impact factor: 3.791

2.  A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death.

Authors:  J C Brackett; H F Sims; R D Steiner; M Nunge; E M Zimmerman; B deMartinville; P Rinaldo; R Slaugh; A W Strauss
Journal:  J Clin Invest       Date:  1994-10       Impact factor: 14.808

3.  Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies.

Authors:  R Ziadeh; E P Hoffman; D N Finegold; R C Hoop; J C Brackett; A W Strauss; E W Naylor
Journal:  Pediatr Res       Date:  1995-05       Impact factor: 3.756
  3 in total
  1 in total

1.  Prospective surveillance study of medium chain acyl-CoA dehydrogenase deficiency in the UK.

Authors:  R J Pollitt; J V Leonard
Journal:  Arch Dis Child       Date:  1998-08       Impact factor: 3.791
  1 in total

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