Literature DB >> 10836898

Is the G985A allelic variant of medium-chain acyl-CoA dehydrogenase a risk factor for sudden infant death syndrome? A pooled analysis.

S S Wang, P M Fernhoff, M J Khoury.   

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Year:  2000        PMID： 10836898     DOI： 10.1542/peds.105.5.1175

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  3 in total

1.  Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency.

Authors:  S Albers; H L Levy; M Irons; A W Strauss; D Marsden
Journal:  J Inherit Metab Dis       Date:  2001-06       Impact factor: 4.982

Review 2.  Newborn screening for medium chain acyl-CoA dehydrogenase deficiency: evaluating the effects on outcome.

Authors:  Carol Dezateux
Journal:  Eur J Pediatr       Date:  2003-11-20       Impact factor: 3.183

3.  Status epilepticus and coma leading to death in a boy caused by Medium-chainacyl-coA dehydrogenase deficiency.

Authors:  Ezatolah Abbasi; Ahad Ghazavi; Masoud Hassanvand Amouzadeh; Mohammad Valizadeh; Mohsen Akhavan Sepahi
Journal:  Iran J Child Neurol       Date:  2021
  3 in total

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