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Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 Years.
Lacour, Morgane; Quenez, Olivier; Rovelet-Lecrux, Anne; Salomon, Bruno; Rousseau, Stephane; Richard, Anne-Claire; Quillard-Muraine, Muriel; Pasquier, Florence; Rollin-Sillaire, Adeline; Martinaud, Olivier; Zarea, Aline; de la Sayette, Vincent; Boutoleau-Bretonniere, Claire; Etcharry-Bouyx, Frédérique; Chauviré, Valérie; Sarazin, Marie; le Ber, Isabelle; Epelbaum, Stéphane; Jonveaux, Thérèse; Rouaud, Olivier; Ceccaldi, Mathieu; Godefroy, Olivier; Formaglio, Maite; Croisile, Bernard; Auriacombe, Sophie; Magnin, Eloi; Sauvée, Mathilde; Marelli, Cecilia; Gabelle, Audrey; Pariente, Jeremie; Paquet, Claire; Boland, Anne; Deleuze, Jean-François; Campion, Dominique; Hannequin, Didier; Nicolas, Gael; Wallon, David.
Afiliación
  • Lacour M; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Neurology and CNR-MAJ, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Quenez O; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Rovelet-Lecrux A; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Salomon B; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Neurology and CNR-MAJ, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Rousseau S; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Richard AC; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Quillard-Muraine M; Normandie Univ, UNIROUEN, Rouen University Hospital, Biochemistry Laboratory, Rouen, France.
  • Pasquier F; Department of Neurology and CNR-MAJ, Lille University Hospital, Lille, France.
  • Rollin-Sillaire A; Univ Lille, Inserm UMR-S 1171, Distalz, Lille, France.
  • Martinaud O; Department of Neurology and CNR-MAJ, Lille University Hospital, Lille, France.
  • Zarea A; Univ Lille, Inserm UMR-S 1171, Distalz, Lille, France.
  • de la Sayette V; Department of Neurology, Caen University Hospital, Caen, France.
  • Boutoleau-Bretonniere C; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Neurology and CNR-MAJ, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Etcharry-Bouyx F; Department of Neurology, Caen University Hospital, Caen, France.
  • Chauviré V; Department of Neurology, Nantes University Hospital, Nantes, France.
  • Sarazin M; Department of Neurology, Angers University Hospital, Angers, France.
  • le Ber I; Department of Neurology, Angers University Hospital, Angers, France.
  • Epelbaum S; Department of Neurology, Saint Anne University Hospital, Paris, France.
  • Jonveaux T; National Reference Center for Rare or Early Dementias and Center of Excellence of Neurodegenerative Disease (CoEN), Institute of Memory and Alzheimer's Disease (IM2A), APHP, Hôpital Pitié-Salpêtrière, Paris, and Sorbonne Universités, UPMC Univ Paris 06, Inserm U1127, CNRS UMR 7225, Brain and Spine I
  • Rouaud O; National Reference Center for Rare or Early Dementias and Center of Excellence of Neurodegenerative Disease (CoEN), Institute of Memory and Alzheimer's Disease (IM2A), APHP, Hôpital Pitié-Salpêtrière, Paris, and Sorbonne Universités, UPMC Univ Paris 06, Inserm U1127, CNRS UMR 7225, Brain and Spine I
  • Ceccaldi M; Department of Geriatrics and CMRR, Nancy University Hospital, Nancy, France.
  • Godefroy O; Department of Neurology, Dijon University Hospital, Dijon, France.
  • Formaglio M; Aix Marseille Univ, INSERM, INS, Inst Neurosci Syst, Service de Neurologie et de Neuropsychologie, CHU de la Timone, APHM, Marseille, France.
  • Croisile B; Departments of Neurology, Amiens University Hospital, and Laboratory of Functional Neurosciences1, 6 (EA 4559), Jules Verne University of Picardie, Amiens, France.
  • Auriacombe S; Service de Neuropsychologie and CMRR, Lyon University Hospital, Lyon, France.
  • Magnin E; Service de Neuropsychologie and CMRR, Lyon University Hospital, Lyon, France.
  • Sauvée M; Department of Neurology, Bordeaux University Hospital, Bordeaux, France.
  • Marelli C; Department of Neurology, Besançon University Hospital, Besançon, France.
  • Gabelle A; Department of Neurology, Grenoble University Hospital, Grenoble, France.
  • Pariente J; Department of Neurology, Montpellier, University Hospital, Montpellier, France.
  • Paquet C; Department of Neurology, Montpellier, University Hospital, Montpellier, France.
  • Boland A; CMRR Department of Neurology, Toulouse University Hospital, Toulouse, France.
  • Deleuze JF; Cognitive Neurology Center/CMRR Paris Nord Ile de France, Lariboisière Fernand-Widal Hospital Université de Paris, INSERMU1144, Paris.
  • Campion D; Centre National de Recherche en Génomique Humaine (CNRGH), Institut de Biologie François Jacob, CEA, Université Paris-Saclay, Evry, France.
  • Hannequin D; Centre National de Recherche en Génomique Humaine (CNRGH), Institut de Biologie François Jacob, CEA, Université Paris-Saclay, Evry, France.
  • Nicolas G; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Wallon D; Department of Research, Centre Hospitalier du Rouvray, Sotteville-lès-Rouen, France.
J Alzheimers Dis ; 71(1): 227-243, 2019.
Article en En | MEDLINE | ID: mdl-31381512
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Enfermedad de Alzheimer / Mutación Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Alzheimers Dis Asunto de la revista: GERIATRIA / NEUROLOGIA Año: 2019 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Enfermedad de Alzheimer / Mutación Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Alzheimers Dis Asunto de la revista: GERIATRIA / NEUROLOGIA Año: 2019 Tipo del documento: Article