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Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatment.
Dufournet, B; Nguyen, K; Charles, P; Grabli, D; Jacquette, A; Borg, M; Danaila, T; Mutez, E; Drapier, S; Colin, O; Eusebio, A; Philip, N; Azulay, J P.
Afiliación
  • Dufournet B; Department of Clinical Neurosciences (Movement Disorders), Timone University Hospital (AP-HM), 264 rue Saint Pierre, 13385 Marseille Cedex 5, France; Aix-Marseille University, Marseille, France. Electronic address: boris.dufournet@ap-hm.fr.
  • Nguyen K; Department of Genetics (Neurogenetics), Timone University Hospital (AP-HM), Marseille, France; Aix-Marseille University, Marseille, France.
  • Charles P; Department of Genetics (Neurogenetics), Pitié-Salpêtrière University Hospital (AP-HP), Paris, France; Sorbonne University, UPMC Paris 06 (UMR S 1127, CNRS UMR 7225, ICM), Paris, France.
  • Grabli D; Department of Neurology (Movement Disorders), Pitié-Salpêtrière University Hospital (AP-HP), Paris, France; Sorbonne University, UPMC Paris 06 (UMR S 1127, CNRS UMR 7225, ICM), Paris, France.
  • Jacquette A; Department of Genetics (Neurogenetics), Pitié-Salpêtrière University Hospital (AP-HP), Paris, France; Sorbonne University, UPMC Paris 06 (UMR S 1127, CNRS UMR 7225, ICM), Paris, France.
  • Borg M; Department of Clinical Neurosciences (Movement Disorders), Nice University Hospital, Nice, France.
  • Danaila T; Department of Neurology (Movement Disorders), Pierre Wertheimer University Hospital (HCL), Lyon, France; Lyon-1 University, Marc Jeannerod Center for Cognitives Neurosciences (CNRS UMR 5229), Lyon, France.
  • Mutez E; Department of Neurosciences (Movement Disorders), Lille University Hospital, Lille, France; Lille University (INSERM U1171), Lille, France.
  • Drapier S; Department of Neurology (Movement Disorders), Rennes University Hospital, Rennes, France; Rennes-1 University (URU 4712 "Basal Ganglia & Behavior"), Rennes, France.
  • Colin O; Department of Neurology (Movement Disorders), Poitiers University Hospital, Poitiers, France; Clinical Investigation Center (INSERM CIC 0802 & INSERM U1084, Clinical and Experimental Neurosciences), Poitiers University Hospital, Poitiers, France.
  • Eusebio A; Department of Clinical Neurosciences (Movement Disorders), Timone University Hospital (AP-HM), 264 rue Saint Pierre, 13385 Marseille Cedex 5, France; Aix-Marseille University, Marseille, France.
  • Philip N; Department of Genetics (Neurogenetics), Timone University Hospital (AP-HM), Marseille, France; Aix-Marseille University, Marseille, France.
  • Azulay JP; Department of Clinical Neurosciences (Movement Disorders), Timone University Hospital (AP-HM), 264 rue Saint Pierre, 13385 Marseille Cedex 5, France; Aix-Marseille University, Marseille, France.
Rev Neurol (Paris) ; 173(6): 406-410, 2017 Jun.
Article en En | MEDLINE | ID: mdl-28461026

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Síndrome de Deleción 22q11 Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Rev Neurol (Paris) Año: 2017 Tipo del documento: Article Pais de publicación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Síndrome de Deleción 22q11 Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Rev Neurol (Paris) Año: 2017 Tipo del documento: Article Pais de publicación: Francia