Literature DB >> 2878195

Sudden infant death syndrome and inherited disorders of fat metabolism.

J P Harpey, C Charpentier, M Paturneau-Jouas.   

Abstract

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Year:  1986        PMID： 2878195     DOI： 10.1016/s0140-6736(86)91455-8

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

1.  Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblings.

Authors:  C Catzeflis; C Bachmann; D E Hale; P M Coates; U Wiesmann; J P Colombo; F Joris; G Délèze
Journal:  Eur J Pediatr       Date:  1990-05       Impact factor: 3.183

Review 2.  Biochemical screening in newborn siblings of cases of SIDS.

Authors:  A Green
Journal:  Arch Dis Child       Date:  1993-06       Impact factor: 3.791

Review 3.  Disorders of mitochondrial beta-oxidation: prenatal and early postnatal diagnosis and their relevance to Reye's syndrome and sudden infant death.

Authors:  R J Pollitt
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982
  3 in total

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