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10. Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease. Alcalay RN; Mejia-Santana H; Tang MX; Rosado L; Verbitsky M; Kisselev S; Ross BM; Louis ED; Comella CL; Colcher A; Jennings D; Nance MA; Bressman S; Scott WK; Tanner C; Mickel SF; Andrews HF; Waters CH; Fahn S; Cote LJ; Frucht SJ; Ford B; Rezak M; Novak K; Friedman JH; Pfeiffer R; Marsh L; Hiner B; Siderowf A; Caccappolo E; Ottman R; Clark LN; Marder KS Arch Neurol; 2009 Dec; 66(12):1517-22. PubMed ID: 20008657 [TBL] [Abstract][Full Text] [Related]
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13. Exhaustion of mitochondrial and autophagic reserve may contribute to the development of LRRK2 Juárez-Flores DL; González-Casacuberta I; Ezquerra M; Bañó M; Carmona-Pontaque F; Catalán-García M; Guitart-Mampel M; Rivero JJ; Tobias E; Milisenda JC; Tolosa E; Marti MJ; Fernández-Santiago R; Cardellach F; Morén C; Garrabou G J Transl Med; 2018 Jun; 16(1):160. PubMed ID: 29884186 [TBL] [Abstract][Full Text] [Related]
14. Altered Development of Synapse Structure and Function in Striatum Caused by Parkinson's Disease-Linked LRRK2-G2019S Mutation. Matikainen-Ankney BA; Kezunovic N; Mesias RE; Tian Y; Williams FM; Huntley GW; Benson DL J Neurosci; 2016 Jul; 36(27):7128-41. PubMed ID: 27383589 [TBL] [Abstract][Full Text] [Related]
15. LRRK2 G2019S Parkinson's disease with more benign phenotype than idiopathic. Ben Romdhan S; Farhat N; Nasri A; Lesage S; Hdiji O; Ben Djebara M; Landoulsi Z; Stevanin G; Brice A; Damak M; Gouider R; Mhiri C Acta Neurol Scand; 2018 Nov; 138(5):425-431. PubMed ID: 29989150 [TBL] [Abstract][Full Text] [Related]
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19. Nonmotor symptoms in LRRK2 G2019S associated Parkinson's disease. Gaig C; Vilas D; Infante J; Sierra M; García-Gorostiaga I; Buongiorno M; Ezquerra M; Martí MJ; Valldeoriola F; Aguilar M; Calopa M; Hernandez-Vara J; Tolosa E PLoS One; 2014; 9(10):e108982. PubMed ID: 25330404 [TBL] [Abstract][Full Text] [Related]
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