Acylcoenzyme A dehydrogenase deficiency in heart tissue from infants who died unexpectedly with fatty change in the liver

Author:

Allison F.,Bennett M J,Variend S,Engel P C

Publisher

BMJ

Subject

General Earth and Planetary Sciences,General Environmental Science,General Engineering

Reference8 articles.

1. Defects in the metabolism of fatty acids in the sudden infant death syndrome;Howat, A.J.; Bennett, M.J.; Vaiend, S.; Shaw, L.; Engel, P.C.;BrMedJ3

2. Sudden infant death and inherited disorders of fat oxidation;Anonymous;Lancet,1986

3. Acyl coenzyme A dehydrogenase;Beinert, H.,1963

4. Inherited disorders of straight chain fatty acid oxidation;Pollitt, R.J.;Arch Dis Child,1987

5. Glutaric aciduria type II: treatment with riboflavin, carnitine and insulin;Mooy, P.D.; Przyrembel, H.; Giesberts, M.A.H.; Scholte, H.R.; Blom, W.; van Gelderen, H.H.;EurJ Pediatr,1984

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