Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria.

Haas, D; Niklowitz, P; Hörster, F; Baumgartner, E R; Prasad, C; Rodenburg, R J; Hoffmann, G F; Menke, T; Okun, J G

Haas, D; Niklowitz, P; Hörster, F; Baumgartner, E R; Prasad, C; Rodenburg, R J; Hoffmann, G F; Menke, T; Okun, J G.

Affiliation

Haas D; Department of General Pediatrics, Division of Inborn Metabolic Diseases, University Children's Hospital, Heidelberg, Germany. dorothea.haas@med.uni-heidelberg.de

J Inherit Metab Dis ; 32(4): 570-5, 2009 Aug.

Article in En | MEDLINE | ID: mdl-19504350

Subject(s)

Fibroblasts/metabolism; Fibroblasts/pathology; Metabolism, Inborn Errors/pathology; Mevalonate Kinase Deficiency/pathology; Ubiquinone/analogs & derivatives; Case-Control Studies; Cells, Cultured; Down-Regulation; Female; Humans; Metabolism, Inborn Errors/metabolism; Methylmalonic Acid/urine; Mevalonate Kinase Deficiency/metabolism; Muscles/metabolism; Muscles/pathology; Ubiquinone/metabolism

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ubiquinone / Mevalonate Kinase Deficiency / Fibroblasts / Metabolism, Inborn Errors Type of study: Observational_studies / Risk_factors_studies Limits: Female / Humans Language: En Journal: J Inherit Metab Dis Year: 2009 Type: Article Affiliation country: Germany

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