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8. LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease. Civitelli D; Tarantino P; Nicoletti G; Cirò Candiano IC; Annesi F; De Marco EV; Carrideo S; Rocca FE; Condino F; Spadafora P; Pugliese P; D'Asero S; Morelli M; Paglionico S; Annesi G; Quattrone A Clin Genet; 2007 Apr; 71(4):367-70. PubMed ID: 17470139 [No Abstract] [Full Text] [Related]
9. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. Ozelius LJ; Senthil G; Saunders-Pullman R; Ohmann E; Deligtisch A; Tagliati M; Hunt AL; Klein C; Henick B; Hailpern SM; Lipton RB; Soto-Valencia J; Risch N; Bressman SB N Engl J Med; 2006 Jan; 354(4):424-5. PubMed ID: 16436782 [No Abstract] [Full Text] [Related]
10. Association of LRRK2 and GBA mutations in a Brazilian family with Parkinson's disease. Spitz M; Pereira JS; Nicareta DH; Abreu Gde M; Bastos EF; Seixas TL; Pimentel MM Parkinsonism Relat Disord; 2015 Jul; 21(7):825-6. PubMed ID: 25952961 [No Abstract] [Full Text] [Related]
11. Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease. Marongiu R; Ghezzi D; Ialongo T; Soleti F; Elia A; Cavone S; Albanese A; Altavista MC; Barone P; Brusa L; Cortelli P; Petrozzi L; Scaglione C; Stanzione P; Tinazzi M; Zeviani M; Dallapiccola B; Bentivoglio AR; Valente EM; Garavaglia B; Mov Disord; 2006 Aug; 21(8):1232-5. PubMed ID: 16622859 [TBL] [Abstract][Full Text] [Related]
12. Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. Nichols WC; Pankratz N; Hernandez D; Paisán-Ruíz C; Jain S; Halter CA; Michaels VE; Reed T; Rudolph A; Shults CW; Singleton A; Foroud T; Lancet; 2005 Jan 29-Feb 4; 365(9457):410-2. PubMed ID: 15680455 [TBL] [Abstract][Full Text] [Related]
13. LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs. Lesage S; Dürr A; Tazir M; Lohmann E; Leutenegger AL; Janin S; Pollak P; Brice A; N Engl J Med; 2006 Jan; 354(4):422-3. PubMed ID: 16436781 [No Abstract] [Full Text] [Related]
14. Mechanistic insight into the dominant mode of the Parkinson's disease-associated G2019S LRRK2 mutation. Luzón-Toro B; Rubio de la Torre E; Delgado A; Pérez-Tur J; Hilfiker S Hum Mol Genet; 2007 Sep; 16(17):2031-9. PubMed ID: 17584768 [TBL] [Abstract][Full Text] [Related]
15. [What can we learn from genes responsible for familial forms of Parkinson's disease?]. Brice A Bull Acad Natl Med; 2006 Feb; 190(2):485-96; discussion 497-8. PubMed ID: 17001874 [TBL] [Abstract][Full Text] [Related]
16. Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation. Kay DM; Kramer P; Higgins D; Zabetian CP; Payami H Mov Disord; 2005 Aug; 20(8):1077-8. PubMed ID: 16001413 [No Abstract] [Full Text] [Related]
17. Clinical genetics of Parkinson's disease and related disorders. Wider C; Wszolek ZK Parkinsonism Relat Disord; 2007; 13 Suppl 3():S229-32. PubMed ID: 18267241 [TBL] [Abstract][Full Text] [Related]
18. [Studies on pathogenesis of Parkinson's disease]. Mizuno Y Nihon Naika Gakkai Zasshi; 2005 Feb; 94 Suppl():66-70. PubMed ID: 15796059 [No Abstract] [Full Text] [Related]
19. [The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients]. Balicza P; Bereznai B; Takáts A; Klivényi P; Dibó G; Hidasi E; Balogh I; Molnár MJ Ideggyogy Sz; 2012 Jul; 65(7-8):239-42. PubMed ID: 23074843 [TBL] [Abstract][Full Text] [Related]
20. The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease. Lu CS; Simons EJ; Wu-Chou YH; Fonzo AD; Chang HC; Chen RS; Weng YH; Rohé CF; Breedveld GJ; Hattori N; Gasser T; Oostra BA; Bonifati V Parkinsonism Relat Disord; 2005 Dec; 11(8):521-2. PubMed ID: 16256409 [No Abstract] [Full Text] [Related] [Next] [New Search]