Related Experiment Videos

Continuation vs discontinuation of diet in phenylketonuria

¹Children's Hospital, Dublin 1, Ireland.

European Journal of Clinical Nutrition

|January 1, 1989

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).

Journal of inherited metabolic disease·2007

Short-chain acyl-CoA dehydrogenase deficiency associated with early onset severe axonal neuropathy.

Neuropediatrics·2004

Glutaric aciduria type I: outcome in the Republic of Ireland.

Journal of inherited metabolic disease·2004

Emergency treatment in glutaryl-CoA dehydrogenase deficiency.

Journal of inherited metabolic disease·2004

Maintenance treatment of glutaryl-CoA dehydrogenase deficiency.

Journal of inherited metabolic disease·2004

Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: a multicenter observational study.

Arteriosclerosis, thrombosis, and vascular biology·2001

See all related articles