Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria.

Cosson, M A; Touati, G; Lacaille, F; Valayannnopoulos, V; Guyot, C; Guest, G; Verkarre, V; Chrétien, D; Rabier, D; Munnich, A; Benoist, J F; de Keyzer, Y; Niaudet, P; de Lonlay, P

Cosson, M A; Touati, G; Lacaille, F; Valayannnopoulos, V; Guyot, C; Guest, G; Verkarre, V; Chrétien, D; Rabier, D; Munnich, A; Benoist, J F; de Keyzer, Y; Niaudet, P; de Lonlay, P.

Affiliation

Cosson MA; Metabolic unit, Reference Center, Necker-Enfants Malades Hospital, University Paris Descartes, 149 rue de Sèvres, 75009 Paris, France.

Mol Genet Metab ; 95(1-2): 107-9, 2008.

Article in En | MEDLINE | ID: mdl-18676166

Subject(s)

Hepatoblastoma/enzymology; Lipid Metabolism, Inborn Errors/complications; Lipid Metabolism, Inborn Errors/enzymology; Methylmalonyl-CoA Mutase/metabolism; Cells, Cultured; Child; Electron Transport; Fatal Outcome; Fibroblasts/enzymology; Follow-Up Studies; Hepatoblastoma/etiology; Hepatoblastoma/genetics; Hepatoblastoma/therapy; Humans; Immunosuppressive Agents/adverse effects; Kidney/enzymology; Kidney/metabolism; Kidney Transplantation/adverse effects; Lipid Metabolism, Inborn Errors/genetics; Lipid Metabolism, Inborn Errors/therapy; Male; Methylmalonic Acid/metabolism; Methylmalonyl-CoA Mutase/genetics; Mutation

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatoblastoma / Lipid Metabolism, Inborn Errors / Methylmalonyl-CoA Mutase Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans / Male Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2008 Type: Article Affiliation country: France

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