138 related articles for article (PubMed ID: 18688798)
21. Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson's disease in a Han-Chinese population in south-eastern China.
Cai J; Lin Y; Chen W; Lin Q; Cai B; Wang N; Zheng W
Neurol Sci; 2013 Nov; 34(11):2001-6. PubMed ID: 23624603
[TBL] [Abstract][Full Text] [Related]
22. The LRRK2 R1628P variant plays a protective role in Han Chinese population with Alzheimer's disease.
Li HL; Lu SJ; Sun YM; Guo QH; Sadovnick AD; Wu ZY
CNS Neurosci Ther; 2013 Apr; 19(4):207-15. PubMed ID: 23421816
[TBL] [Abstract][Full Text] [Related]
23. A novel P755L mutation in LRRK2 gene associated with Parkinson's disease.
Wu T; Zeng Y; Ding X; Li X; Li W; Dong H; Chen S; Zhang X; Ma G; Yao J; Deng X
Neuroreport; 2006 Dec; 17(18):1859-62. PubMed ID: 17179858
[TBL] [Abstract][Full Text] [Related]
24. An association analysis of the R1628P and G2385R polymorphisms of the LRRK2 gene in multiple system atrophy in a Chinese population.
Yuan X; Chen Y; Cao B; Zhao B; Wei Q; Guo X; Yang Y; Yuan L; Shang H
Parkinsonism Relat Disord; 2015 Feb; 21(2):147-9. PubMed ID: 25511328
[TBL] [Abstract][Full Text] [Related]
25. A study of six point mutation analysis of LRRK2 gene in Chinese mainland patients with Parkinson's disease.
Hu ZX; Peng DT; Cai M; Pu JL; Lei XG; Yin XZ; Ou-Yang ZY; Luo W; Zhang BR
Neurol Sci; 2011 Aug; 32(4):741-2. PubMed ID: 21234781
[No Abstract] [Full Text] [Related]
26. Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians.
Tan EK; Zhao Y; Tan L; Lim HQ; Lee J; Yuen Y; Pavanni R; Wong MC; Fook-Chong S; Liu JJ
Mov Disord; 2007 Sep; 22(12):1816-8. PubMed ID: 17659642
[TBL] [Abstract][Full Text] [Related]
27. Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease.
Toft M; Mata IF; Ross OA; Kachergus J; Hulihan MM; Haugarvoll K; Stone JT; Blazquez M; Gibson JM; Aasly JO; White LR; Lynch T; Adler CH; Gwinn-Hardy K; Farrer MJ
Mov Disord; 2007 Feb; 22(3):389-92. PubMed ID: 17216639
[TBL] [Abstract][Full Text] [Related]
28. LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China.
Yu L; Hu F; Zou X; Jiang Y; Liu Y; He X; Xi J; Liu L; Liu Z; He L; Xu Y
Brain Res; 2009 Nov; 1296():113-6. PubMed ID: 19699188
[TBL] [Abstract][Full Text] [Related]
29. New LRRK2 variants identified in Parkinson's disease.
Tan EK; Schapira AH
Eur J Neurol; 2011 Mar; 18(3):369-70. PubMed ID: 20629720
[No Abstract] [Full Text] [Related]
30. Association of LRRK2 R1628P variant with Parkinson's disease in Ethnic Han-Chinese and subgroup population.
Zhang P; Wang Q; Jiao F; Yan J; Chen L; He F; Zhang Q; Tian B
Sci Rep; 2016 Nov; 6():35171. PubMed ID: 27812003
[TBL] [Abstract][Full Text] [Related]
31. SNCA but not DNM3 and GAK modifies age at onset of LRRK2-related Parkinson's disease in Chinese population.
Yang ZH; Li YS; Shi MM; Yang J; Liu YT; Mao CY; Fan Y; Hu XC; Shi CH; Xu YM
J Neurol; 2019 Jul; 266(7):1796-1800. PubMed ID: 31041581
[TBL] [Abstract][Full Text] [Related]
32. A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease.
Wang L; Guo JF; Nie LL; Xu Q; Zuo X; Sun QY; Yan XX; Tang BS
Neurosci Lett; 2010 Jan; 468(3):198-201. PubMed ID: 19879329
[TBL] [Abstract][Full Text] [Related]
33. Lrrk2 R1628P variant is a risk factor for essential tremor.
Chao YX; Ng EY; Tan L; Prakash KM; Au WL; Zhao Y; Tan EK
Sci Rep; 2015 Mar; 5():9029. PubMed ID: 25761573
[TBL] [Abstract][Full Text] [Related]
34. The LRRK2 gene is mutated in a Chinese autosomal-dominant Parkinson's disease family.
Guo R; Hu X; Chen Q; Zhang Y; Zhang Y; Sun Y; Hu G
Genet Test Mol Biomarkers; 2013 Feb; 17(2):131-4. PubMed ID: 23268655
[TBL] [Abstract][Full Text] [Related]
35. LRRK2 variant associated with Alzheimer's disease.
Zhao Y; Ho P; Yih Y; Chen C; Lee WL; Tan EK
Neurobiol Aging; 2011 Nov; 32(11):1990-3. PubMed ID: 20018409
[TBL] [Abstract][Full Text] [Related]
36. Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.
Ross OA; Soto-Ortolaza AI; Heckman MG; Aasly JO; Abahuni N; Annesi G; Bacon JA; Bardien S; Bozi M; Brice A; Brighina L; Van Broeckhoven C; Carr J; Chartier-Harlin MC; Dardiotis E; Dickson DW; Diehl NN; Elbaz A; Ferrarese C; Ferraris A; Fiske B; Gibson JM; Gibson R; Hadjigeorgiou GM; Hattori N; Ioannidis JP; Jasinska-Myga B; Jeon BS; Kim YJ; Klein C; Kruger R; Kyratzi E; Lesage S; Lin CH; Lynch T; Maraganore DM; Mellick GD; Mutez E; Nilsson C; Opala G; Park SS; Puschmann A; Quattrone A; Sharma M; Silburn PA; Sohn YH; Stefanis L; Tadic V; Theuns J; Tomiyama H; Uitti RJ; Valente EM; van de Loo S; Vassilatis DK; Vilariño-Güell C; White LR; Wirdefeldt K; Wszolek ZK; Wu RM; Farrer MJ;
Lancet Neurol; 2011 Oct; 10(10):898-908. PubMed ID: 21885347
[TBL] [Abstract][Full Text] [Related]
37. Penetrance in Parkinson's disease related to the LRRK2 R1441G mutation in the Basque country (Spain).
Ruiz-Martínez J; Gorostidi A; Ibañez B; Alzualde A; Otaegui D; Moreno F; López de Munain A; Bergareche A; Gómez-Esteban JC; Martí Massó JF
Mov Disord; 2010 Oct; 25(14):2340-5. PubMed ID: 20721916
[TBL] [Abstract][Full Text] [Related]
38. Genetic variants ofLRRK2 in Taiwanese Parkinson's disease.
Wu YR; Chang KH; Chang WT; Hsiao YC; Hsu HC; Jiang PR; Chen YC; Chao CY; Chang YC; Lee BH; Hu FJ; Chen WL; Lee-Chen GJ; Chen CM
PLoS One; 2013; 8(12):e82001. PubMed ID: 24339985
[TBL] [Abstract][Full Text] [Related]
39. LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation.
Lorenzo-Betancor O; Samaranch L; Ezquerra M; Tolosa E; Lorenzo E; Irigoyen J; Gaig C; Pastor MA; Soto-Ortolaza AI; Ross OA; Rodríguez-Oroz MC; Valldeoriola F; Martí MJ; Luquin MR; Perez-Tur J; Burguera JA; Obeso JA; Pastor P
Mov Disord; 2012 Jan; 27(1):146-51. PubMed ID: 22038903
[TBL] [Abstract][Full Text] [Related]
40. LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.
Gaig C; Ezquerra M; Marti MJ; Muñoz E; Valldeoriola F; Tolosa E
Arch Neurol; 2006 Mar; 63(3):377-82. PubMed ID: 16533964
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]