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Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry.
Lee, Annie J; Wang, Yuanjia; Alcalay, Roy N; Mejia-Santana, Helen; Saunders-Pullman, Rachel; Bressman, Susan; Corvol, Jean-Christophe; Brice, Alexis; Lesage, Suzanne; Mangone, Graziella; Tolosa, Eduardo; Pont-Sunyer, Claustre; Vilas, Dolores; Schüle, Birgitt; Kausar, Farah; Foroud, Tatiana; Berg, Daniela; Brockmann, Kathrin; Goldwurm, Stefano; Siri, Chiara; Asselta, Rosanna; Ruiz-Martinez, Javier; Mondragón, Elisabet; Marras, Connie; Ghate, Taneera; Giladi, Nir; Mirelman, Anat; Marder, Karen.
Afiliação
  • Lee AJ; Department of Biostatistics, Mailman School of Public Health, Columbia University, New York, New York, USA.
  • Wang Y; Department of Biostatistics, Mailman School of Public Health, Columbia University, New York, New York, USA.
  • Alcalay RN; Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, New York, USA.
  • Mejia-Santana H; Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, New York, USA.
  • Saunders-Pullman R; Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, New York, USA.
  • Bressman S; Department of Neurology, Mount Sinai Beth Israel Medical Center, New York, New York, USA.
  • Corvol JC; Department of Neurology, Mount Sinai Beth Israel Medical Center, New York, New York, USA.
  • Brice A; Sorbonne Universités, Université Pierre et Marie Curie (UPMC Univ) Paris 06.
  • Lesage S; Institut National de la Santé et de la Recherche Médicale, U1127, Paris, France.
  • Mangone G; Centre National de la Recherche Scientifique, UMR 7225, Paris, France.
  • Tolosa E; Institut du Cerveau et de la Moelle Epinière (ICM), Hôpital Pitié-Salpêtrière, Département des maladies du système nerveux, F-75013, Paris, France.
  • Pont-Sunyer C; Department of Neurology, Institut National de la Santé et de la Recherche Médicale, Assistance-Publique Hôpitaux de Paris, CIC-1422, Hôpital Pitié-Salpêtrière, Paris, France.
  • Vilas D; Assistance publique - Hôpitaux de Paris (AP-HP), 75015, Paris, France.
  • Schüle B; Sorbonne Universités, Université Pierre et Marie Curie (UPMC Univ) Paris 06.
  • Kausar F; Institut National de la Santé et de la Recherche Médicale, U1127, Paris, France.
  • Foroud T; Centre National de la Recherche Scientifique, UMR 7225, Paris, France.
  • Berg D; Institut du Cerveau et de la Moelle Epinière (ICM), Hôpital Pitié-Salpêtrière, Département des maladies du système nerveux, F-75013, Paris, France.
  • Brockmann K; Department of Neurology, Institut National de la Santé et de la Recherche Médicale, Assistance-Publique Hôpitaux de Paris, CIC-1422, Hôpital Pitié-Salpêtrière, Paris, France.
  • Goldwurm S; Assistance publique - Hôpitaux de Paris (AP-HP), 75015, Paris, France.
  • Siri C; Sorbonne Universités, Université Pierre et Marie Curie (UPMC Univ) Paris 06.
  • Asselta R; Institut National de la Santé et de la Recherche Médicale, U1127, Paris, France.
  • Ruiz-Martinez J; Centre National de la Recherche Scientifique, UMR 7225, Paris, France.
  • Mondragón E; Institut du Cerveau et de la Moelle Epinière (ICM), Hôpital Pitié-Salpêtrière, Département des maladies du système nerveux, F-75013, Paris, France.
  • Marras C; Department of Neurology, Institut National de la Santé et de la Recherche Médicale, Assistance-Publique Hôpitaux de Paris, CIC-1422, Hôpital Pitié-Salpêtrière, Paris, France.
  • Ghate T; Assistance publique - Hôpitaux de Paris (AP-HP), 75015, Paris, France.
  • Giladi N; Sorbonne Universités, Université Pierre et Marie Curie (UPMC Univ) Paris 06.
  • Mirelman A; Institut National de la Santé et de la Recherche Médicale, U1127, Paris, France.
  • Marder K; Centre National de la Recherche Scientifique, UMR 7225, Paris, France.
Mov Disord ; 32(10): 1432-1438, 2017 Oct.
Article em En | MEDLINE | ID: mdl-28639421
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença / Serina-Treonina Proteína Quinase-2 com Repetições Ricas em Leucina / Mutação Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença / Serina-Treonina Proteína Quinase-2 com Repetições Ricas em Leucina / Mutação Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article