Literature DB >> 2878332

Screening siblings for inborn errors of fatty acid metabolism in families with a history of sudden infant death.

M J Bennett, S Variend, R J Pollitt.   

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Year:  1986        PMID： 2878332     DOI： 10.1016/s0140-6736(86)92794-7

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


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  4 in total

Review 1.  Biochemical screening in newborn siblings of cases of SIDS.

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

Review 2.  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.  The phenylpropionic acid load test: experience with 72 children at-risk for beta-oxidation disorders.

Authors:  J F Glasgow; R Moore; P H Robinson; P J McKiernan
Journal:  Ir J Med Sci       Date:  1992-10       Impact factor: 1.568

4.  Medium-chain acyl CoA dehydrogenase deficiency: Its relationship to SIDS and the impact on genetic counseling.

Authors:  A McConkie-Rosell; A K Iafolla
Journal:  J Genet Couns       Date:  1993-03       Impact factor: 2.537
  4 in total

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