Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups.

Author:

Roe C R,Hoppel C L,Stacey T E,Chalmers R A,Tracey B M,Millington D S

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference21 articles.

1. L-Carnitine therapy in propionicacidaemia (letter);Roe, C.R.; Bohan, T.P.;Lancet,1982

2. Dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl CoA dehydrogenation defects;Pediatr Res,1982

3. Hypocarnitinaemia in disorders of organic acid metabolism (letter);Allen, R.J.; Hansch, D.B.; Wu, H.L.C.;Lancet,1982

4. Organic acids in man. The analytical chemistry, biochemistry and diagnosis of the organic acidurias;Chalmers, R.A.; Lawson, A.M.,1982

5. Carnitine metabolism in the fasting rat;Brass, E.P.; Hoppel, C.L.;JBiol Chem,1978

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