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High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington's disease expansion mutation carriers shows normal mitochondrial respiratory function.
Buck, Eva; Zügel, Martina; Schumann, Uwe; Merz, Tamara; Gumpp, Anja M; Witting, Anke; Steinacker, Jürgen M; Landwehrmeyer, G Bernhard; Weydt, Patrick; Calzia, Enrico; Lindenberg, Katrin S.
Afiliação
  • Buck E; Department of Neurology, Ulm University, Ulm, Germany.
  • Zügel M; Division of Sports- and Rehabilitation Medicine, Ulm University Medical Center, Ulm, Germany.
  • Schumann U; Division of Sports- and Rehabilitation Medicine, Ulm University Medical Center, Ulm, Germany.
  • Merz T; Department of Neurology, Ulm University, Ulm, Germany.
  • Gumpp AM; Department of Neurology, Ulm University, Ulm, Germany.
  • Witting A; Department of Neurology, Ulm University, Ulm, Germany.
  • Steinacker JM; Division of Sports- and Rehabilitation Medicine, Ulm University Medical Center, Ulm, Germany.
  • Landwehrmeyer GB; Department of Neurology, Ulm University, Ulm, Germany.
  • Weydt P; Department of Neurology, Ulm University, Ulm, Germany.
  • Calzia E; Department of Neurodegenerative Diseases, Bonn University, Bonn, Germany.
  • Lindenberg KS; Institute of Anesthesiological Pathophysiology and Process Development, Ulm University, Ulm, Germany.
PLoS One ; 12(4): e0175248, 2017.
Article em En | MEDLINE | ID: mdl-28406926
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Consumo de Oxigênio / Doença de Huntington / Músculo Esquelético / Proteína Huntingtina / Mitocôndrias Musculares / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Animals / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Consumo de Oxigênio / Doença de Huntington / Músculo Esquelético / Proteína Huntingtina / Mitocôndrias Musculares / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Animals / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha