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Myocardial glucose uptake in patients with the m.3243A > G mutation in mitochondrial DNA.
Lindroos, Markus M; Pärkkä, Jussi P; Taittonen, Markku T; Iozzo, Patricia; Kärppä, Mikko; Hassinen, Ilmo E; Knuuti, Juhani; Nuutila, Pirjo; Majamaa, Kari.
Afiliação
  • Lindroos MM; Turku PET Centre, University of Turku, Turku, Finland.
  • Pärkkä JP; Department of Clinical Physiology, Turku University Hospital, Turku, Finland.
  • Taittonen MT; Department of Anaesthesiology, Turku University Hospital, Turku, Finland.
  • Iozzo P; Institute of Clinical Physiology, National Research Council (CNR), Pisa, Italy.
  • Kärppä M; Research Group of Clinical Neuroscience, Neurology, University of Oulu, P.O Box 5000, FIN-90014, Oulu, Finland.
  • Hassinen IE; Medical Research Center Oulu, University of Oulu and Oulu University Hospital, Oulu, Finland.
  • Knuuti J; Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.
  • Nuutila P; Turku PET Centre, University of Turku, Turku, Finland.
  • Majamaa K; Turku PET Centre, University of Turku, Turku, Finland.
J Inherit Metab Dis ; 39(1): 67-74, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26112752

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Glucose / Mitocôndrias / Mutação / Miocárdio Tipo de estudo: Observational_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Inherit Metab Dis Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Finlândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Glucose / Mitocôndrias / Mutação / Miocárdio Tipo de estudo: Observational_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Inherit Metab Dis Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Finlândia