Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Dyskinesias and LRRK2[original query] |
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Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease? Neurology 2008 Nov 71 (19): 1550-2. Lesage S, Belarbi S, Troiano A, Condroyer C, Hecham N, Pollak P, Lohman E, Benhassine T, Ysmail-Dahlouk F, Dürr A, Tazir M, Brice A, |
Dyskinesias in patients with Parkinson's disease: effect of the leucine-rich repeat kinase 2 (LRRK2) G2019S mutation. Parkinsonism & related disorders 2012 Nov 18 (9): 1039-41. Yahalom Gilad, Kaplan Natalie, Vituri Aya, Cohen Oren S, Inzelberg Rivka, Kozlova Evgenia, Korczyn Amos D, Rosset Saharon, Friedman Eitan, Hassin-Baer Shar |
The LRRK2 G2019S mutation in a series of Argentinean patients with Parkinson's disease: clinical and demographic characteristics. Neuroscience letters 2013 Jan . Mabel GE, Virginia P, Paola CD, José PJ, Cecilia CM, Felix MM, Coro PR |
Genetic mutations in Parkinson's disease: screening of a selected population from North-Eastern Italy. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2024 7 . Giulia Bonato, Angelo Antonini, Francesca Pistonesi, Marta Campagnolo, Andrea Guerra, Roberta Biundo, Manuela Pilleri, Cinzia Bertolin, Leonardo Salviati, Miryam Carecch |
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