Inherited metabolic diseases in the sudden infant death syndrome.

Author:

Holton J B,Allen J T,Green C A,Partington S,Gilbert R E,Berry P J

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference16 articles.

1. Deficiency of medium chain acylcoenzyme A dehydrogenase presenting as sudden infant death syndrome;Howat, A.J.; Bennett, M.J.; Variend, S.; Shaw, L.;BMJ,1984

2. Investigation of inborn errors of metabolism in unexpected infant deaths;Emery, J.E.; Howat, A.J.; Variend, S.; Vawter, G.F.;Lancet,1988

3. Pathological investigations in cases of sudden infant death syndrome;Wrigglesworth, J.S.; Keeling, J.W.; Rushton, D.I.; Berry, P.J.;J Clin Pathol,1987

4. Organic acids in man;Chalmers, R.A.; Lawson, A.M.,1982

5. Amino acids and related compounds;Ersser, R.S.; Smith, I.,1976

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