LRRK2 G2019S mutation in Parkinson’s disease: A neuropsychological and neuropsychiatric study in a large Algerian cohort

Parkinsonism & Related Disorders - Tập 16 - Trang 676-679 - 2010
Soreya Belarbi1, Nassima Hecham1, Suzanne Lesage2, Mohamed I. Kediha1, Nourredine Smail3, Traki Benhassine4, Farida Ysmail-Dahlouk1, Ebba Lohman2, Badia Benhabyles3, Tarik Hamadouche5, Salima Assami1, Alexis Brice2, Meriem Tazir1
1Laboratoire de Recherche en Neurosciences, Service de Neurologie, CHU Mustapha, Place du 1er Mai, Algiers 16000, Algeria
2INSERM UMR_S975 (formerly UMR_S679), Department of Genetics, Cytogenetics and Embryology, Pitié- Salpetrière Hospital, Paris, France
3Department of Epidemiology, CHU Mustapha, Algiers, Algeria
4Genetics Laboratory, FSB, Université Bab Ezzouar, Algiers, Algeria
5Molecular Biology Laboratory, Université M’hamed Bougara, Boumerdes, Algeria

Tài liệu tham khảo

Eriksen, 2005, Molecular pathogenesis of Parkinson’s disease, Arch Neurol, 62, 353, 10.1001/archneur.62.3.353 Elbaz, 1999, Familial aggregation of Parkinson’s disease: a population-based case-control study in Europe. EUROPARKINSON study group, Neurology, 52, 1876, 10.1212/WNL.52.9.1876 Lesage, 2009, Parkinson’s disease: from monogenic forms to genetic susceptibility factors, Hum Mol Genet, 18, 48, 10.1093/hmg/ddp012 Lesage, 2006, LRRK2 G2019S as a cause of Parkinson’s disease in North African Arabs, N Engl J Med, 354, 422, 10.1056/NEJMc055540 Brice, 2005, Genetics of Parkinson’s disease: LRRK2 on the rise, Brain, 128, 2760, 10.1093/brain/awh676 Ozelius, 2006, LRRK2 G2019S as a cause of Parkinson’s disease in Ashkenazi Jews, N Engl J Med, 354, 424, 10.1056/NEJMc055509 Lesage, 2008, Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson’s disease?, Neurology, 71, 1550, 10.1212/01.wnl.0000338460.89796.06 Lechevallier-Michel, 2004, Normative data for the MMSE, the Benton visual retention test, the Isaacs’s set test, the digit symbol substitution test and the Zazzo’s cancellation task in subjects over the age 70: results from the PAQUID Study, Rev Neurol (Paris), 160, 1059, 10.1016/S0035-3787(04)71143-1 Dessi, 2009, Assessment of episodic memory in illiterate elderly, Psychol Neuropsychiatr Vieil, 7, 287 Buschke, 1999, Screening for dementia with the memory impairment screen, Neurology, 52, 231, 10.1212/WNL.52.2.231 Goldwurm, 2006, LRRK2 G2019S mutation and Parkinson’s disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sample, Parkinsonism Relat Disord, 12, 410, 10.1016/j.parkreldis.2006.04.001 Lesage, 2005, G2019S LRRK2 mutation in French and North African families with Parkinson’s disease, Ann Neurol, 58, 784, 10.1002/ana.20636 Ngandu, 2007, Education and dementia: what lies behind the association?, Neurology, 69, 1442, 10.1212/01.wnl.0000277456.29440.16 Remy, 2005, Depression in Parkinson’s disease: loss of dopamine and noradrenaline innervation in the limbic system, Brain, 128, 1314, 10.1093/brain/awh445 Kumar, 2002, Sleep disorders in Parkinson’s disease, Mov Disord, 17, 775, 10.1002/mds.10167 Allain, 2005, Rôle de l’âge sur les performances à quatre tests explorant le fonctionnement exécutif. Résultats chez les sujets sains, L’année gérontologique, 78