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

Kölker, S; Christensen, E; Leonard, J V; Greenberg, C R; Burlina, A B; Burlina, A P; Dixon, M; Duran, M; Goodman, S I; Koeller, D M; Müller, E; Naughten, E R; Neumaier-Probst, E; Okun, J G; Kyllerman, M; Surtees, R A; Wilcken, B; Hoffmann, G F; Burgard, P

Kölker, S; Christensen, E; Leonard, J V; Greenberg, C R; Burlina, A B; Burlina, A P; Dixon, M; Duran, M; Goodman, S I; Koeller, D M; Müller, E; Naughten, E R; Neumaier-Probst, E; Okun, J G; Kyllerman, M; Surtees, R A; Wilcken, B; Hoffmann, G F; Burgard, P.

Affiliation

Kölker S; Department of General Pediatrics, Division of Inborn Metabolic Diseases, University Children's Hospital, Heidelberg, Germany. Stefan.Koelker@med.uni-heidelberg.de

J Inherit Metab Dis ; 30(1): 5-22, 2007 Feb.

Article in En | MEDLINE | ID: mdl-17203377

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Collection: 01-internacional Database: MEDLINE Main subject: Glutaryl-CoA Dehydrogenase / Metabolism, Inborn Errors Type of study: Diagnostic_studies / Etiology_studies / Guideline / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Infant / Newborn Language: En Journal: J Inherit Metab Dis Year: 2007 Document type: Article Affiliation country: Country of publication:

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