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7. The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect? Orr-Urtreger A; Shifrin C; Rozovski U; Rosner S; Bercovich D; Gurevich T; Yagev-More H; Bar-Shira A; Giladi N Neurology; 2007 Oct; 69(16):1595-602. PubMed ID: 17938369 [TBL] [Abstract][Full Text] [Related]
8. Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations. Alcalay RN; Levy OA; Waters CC; Fahn S; Ford B; Kuo SH; Mazzoni P; Pauciulo MW; Nichols WC; Gan-Or Z; Rouleau GA; Chung WK; Wolf P; Oliva P; Keutzer J; Marder K; Zhang X Brain; 2015 Sep; 138(Pt 9):2648-58. PubMed ID: 26117366 [TBL] [Abstract][Full Text] [Related]
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11. Genetic screening for two LRRK2 mutations in French patients with idiopathic Parkinson's disease. Funalot B; Nichols WC; Pérez-Tur J; Mercier G; Lucotte G Genet Test; 2006; 10(4):290-3. PubMed ID: 17253937 [TBL] [Abstract][Full Text] [Related]
12. Olfactory dysfunction in LRRK2 G2019S mutation carriers. Saunders-Pullman R; Stanley K; Wang C; San Luciano M; Shanker V; Hunt A; Severt L; Raymond D; Ozelius LJ; Lipton RB; Bressman SB Neurology; 2011 Jul; 77(4):319-24. PubMed ID: 21753159 [TBL] [Abstract][Full Text] [Related]
13. Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients. Floris G; Cannas A; Solla P; Murru MR; Tranquilli S; Corongiu D; Rolesu M; Cuccu S; Sardu C; Marrosu F; Marrosu MG Parkinsonism Relat Disord; 2009 May; 15(4):277-80. PubMed ID: 18805725 [TBL] [Abstract][Full Text] [Related]
14. A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia. Illarioshkin SN; Shadrina MI; Slominsky PA; Bespalova EV; Zagorovskaya TB; Bagyeva GKh; Markova ED; Limborska SA; Ivanova-Smolenskaya IA Eur J Neurol; 2007 Apr; 14(4):413-7. PubMed ID: 17388990 [TBL] [Abstract][Full Text] [Related]
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