Your browser doesn't support javascript.
loading
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype.
Jabbari, Edwin; Woodside, John; Tan, Manuela M X; Shoai, Maryam; Pittman, Alan; Ferrari, Raffaele; Mok, Kin Y; Zhang, David; Reynolds, Regina H; de Silva, Rohan; Grimm, Max-Joseph; Respondek, Gesine; Müller, Ulrich; Al-Sarraj, Safa; Gentleman, Stephen M; Lees, Andrew J; Warner, Thomas T; Hardy, John; Revesz, Tamas; Höglinger, Günter U; Holton, Janice L; Ryten, Mina; Morris, Huw R.
Afiliação
  • Jabbari E; Department of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London, United Kingdom.
  • Woodside J; Department of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London, United Kingdom.
  • Tan MMX; Department of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London, United Kingdom.
  • Shoai M; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, United Kingdom.
  • Pittman A; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, United Kingdom.
  • Ferrari R; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, United Kingdom.
  • Mok KY; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, United Kingdom.
  • Zhang D; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, United Kingdom.
  • Reynolds RH; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, United Kingdom.
  • de Silva R; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, United Kingdom.
  • Grimm MJ; Reta Lila Weston Institute, UCL Institute of Neurology, London, United Kingdom.
  • Respondek G; Department of Translational Neurodegeneration, German Center for Neurodegenerative Diseases (DZNE); Department of Neurology, Technical University of Munich; Munich Cluster for Systems Neurology SyNergy, Munich, Germany.
  • Müller U; Department of Translational Neurodegeneration, German Center for Neurodegenerative Diseases (DZNE); Department of Neurology, Technical University of Munich; Munich Cluster for Systems Neurology SyNergy, Munich, Germany.
  • Al-Sarraj S; Institute for Human Genetics, Justus Liebig University, Giessen, Germany.
  • Gentleman SM; MRC London Neurodegenerative Diseases Brain Bank, Institute of Psychiatry, King's College London, London, United Kingdom.
  • Lees AJ; Multiple Sclerosis and Parkinson's UK Brain Bank, Division of Brain Sciences, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom.
  • Warner TT; Reta Lila Weston Institute, UCL Institute of Neurology, London, United Kingdom.
  • Hardy J; Queen Square Brain Bank for Neurological Disorders, UCL Institute of Neurology, London, United Kingdom.
  • Revesz T; Reta Lila Weston Institute, UCL Institute of Neurology, London, United Kingdom.
  • Höglinger GU; Queen Square Brain Bank for Neurological Disorders, UCL Institute of Neurology, London, United Kingdom.
  • Holton JL; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, United Kingdom.
  • Ryten M; Reta Lila Weston Institute, UCL Institute of Neurology, London, United Kingdom.
  • Morris HR; Queen Square Brain Bank for Neurological Disorders, UCL Institute of Neurology, London, United Kingdom.
Ann Neurol ; 84(4): 485-496, 2018 10.
Article em En | MEDLINE | ID: mdl-30066433
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Variação Genética / Paralisia Supranuclear Progressiva / Ubiquitina-Proteína Ligases / Loci Gênicos / Proteínas com Motivo Tripartido Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Variação Genética / Paralisia Supranuclear Progressiva / Ubiquitina-Proteína Ligases / Loci Gênicos / Proteínas com Motivo Tripartido Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article