Medium chain acyl-CoA dehydrogenase deficiency.

Author:

Touma E H,Charpentier C

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference43 articles.

1. Medium-chain acylCoA dehydrogenase (M-CAD) deficiency in children with non-ketotic hypoglycemia and low carnitine levels;Stanley, C.A.; Hale, D.E.; Coates, P.M.;Pediatr Res,1983

2. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency;Stanley, C.A.;Adv Pediatr,1987

3. Acyl-coA dehydrogenase deficiencies;Roe, C.R.; Coates, P.M.,1989

4. Suberylglycine excretion in the urine from a patient with dicarboxylic acidura;Gregersen, N.; Lauritzen, R.; Rasmussen, K.;Clin Chim Acta,1976

5. Non-ketotic C6-C10 dicarboxylic aciduria: biochemical investigation of two cases;Gregersen, N.; Rosleff, F.; Kolvraa, S.; Hobolth, N.; Rasmussen, K.; Lauritzen, R.;Clin Chim Acta,1980

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