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The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis.
Gang, Qiang; Bettencourt, Conceicao; Machado, Pedro M; Fox, Zoe; Brady, Stefen; Healy, Estelle; Parton, Matt; Holton, Janice L; Hilton-Jones, David; Shieh, Perry B; Zanoteli, Edmar; De Paepe, Boel; De Bleecker, Jan; Shaibani, Aziz; Ripolone, Michela; Violano, Raffaella; Moggio, Maurizio; Barohn, Richard J; Dimachkie, Mazen M; Mora, Marina; Mantegazza, Renato; Zanotti, Simona; Hanna, Michael G; Houlden, Henry.
Afiliação
  • Gang Q; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK; Medical Research Council Centre for Neuromuscular Diseases, Institute of Neurology, University College London, London, UK.
  • Bettencourt C; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK.
  • Machado PM; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK; Medical Research Council Centre for Neuromuscular Diseases, Institute of Neurology, University College London, London, UK.
  • Fox Z; Biomedical Research Centre, UCL and the Education Unit, Institute of Neurology, University College London, London, UK.
  • Brady S; Medical Research Council Centre for Neuromuscular Diseases, Institute of Neurology, University College London, London, UK; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
  • Healy E; Medical Research Council Centre for Neuromuscular Diseases, Institute of Neurology, University College London, London, UK.
  • Parton M; Medical Research Council Centre for Neuromuscular Diseases, Institute of Neurology, University College London, London, UK.
  • Holton JL; Medical Research Council Centre for Neuromuscular Diseases, Institute of Neurology, University College London, London, UK.
  • Hilton-Jones D; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
  • Shieh PB; Neuromuscular Division, Department of Neurology, University of California, Los Angeles Medical Centre, Los Angeles, CA, USA.
  • Zanoteli E; Department of Neurology, Medical School of the University of São Paulo (FMUSP), São Paulo, Brazil.
  • De Paepe B; Department of Neurology and Neuromuscular Reference Centre, Ghent University Hospital, Ghent, Belgium.
  • De Bleecker J; Department of Neurology and Neuromuscular Reference Centre, Ghent University Hospital, Ghent, Belgium.
  • Shaibani A; Nerve and Muscle Centre of Texas, Houston, TX, USA.
  • Ripolone M; Neuromuscular Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Dino Ferrari Centre, University of Milan, Milan, Italy.
  • Violano R; Neuromuscular Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Dino Ferrari Centre, University of Milan, Milan, Italy.
  • Moggio M; Neuromuscular Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Dino Ferrari Centre, University of Milan, Milan, Italy.
  • Barohn RJ; The University of Kansas Medical Centre, Kansas City, USA.
  • Dimachkie MM; The University of Kansas Medical Centre, Kansas City, USA.
  • Mora M; Neuromuscular Diseases and Neuroimmunology Unit, Fondazione IRCCS Isitituto Neurologico C. Besta, Milan, Italy.
  • Mantegazza R; Neuromuscular Diseases and Neuroimmunology Unit, Fondazione IRCCS Isitituto Neurologico C. Besta, Milan, Italy.
  • Zanotti S; Neuromuscular Diseases and Neuroimmunology Unit, Fondazione IRCCS Isitituto Neurologico C. Besta, Milan, Italy.
  • Hanna MG; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK; Medical Research Council Centre for Neuromuscular Diseases, Institute of Neurology, University College London, London, UK.
  • Houlden H; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK; Medical Research Council Centre for Neuromuscular Diseases, Institute of Neurology, University College London, London, UK. Electronic address: h.houlden@ucl.ac.uk.
Neurobiol Aging ; 36(4): 1766.e1-1766.e3, 2015 Apr.
Article em En | MEDLINE | ID: mdl-25670332
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Proteínas de Membrana Transportadoras / Íntrons / Miosite de Corpos de Inclusão / Estudos de Associação Genética / Genótipo Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Proteínas de Membrana Transportadoras / Íntrons / Miosite de Corpos de Inclusão / Estudos de Associação Genética / Genótipo Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article