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Results: 1 to 20 of 186

Similar articles for PubMed (Select 20673920)

1.

LRRK2 Gly2385Arg polymorphism, cigarette smoking, and risk of sporadic Parkinson's disease: a case-control study in Japan.

Miyake Y, Tsuboi Y, Koyanagi M, Fujimoto T, Shirasawa S, Kiyohara C, Tanaka K, Fukushima W, Sasaki S, Yamada T, Oeda T, Miki T, Kawamura N, Sakae N, Fukuyama H, Hirota Y, Nagai M; Fukuoka Kinki Parkinson's Disease Study Group.

J Neurol Sci. 2010 Oct 15;297(1-2):15-8. doi: 10.1016/j.jns.2010.07.002. Epub 2010 Jul 31.

PMID:
20673920
2.

SNCA polymorphisms, smoking, and sporadic Parkinson's disease in Japanese.

Miyake Y, Tanaka K, Fukushima W, Kiyohara C, Sasaki S, Tsuboi Y, Yamada T, Oeda T, Shimada H, Kawamura N, Sakae N, Fukuyama H, Hirota Y, Nagai M; Fukuoka Kinki Parkinson's Disease Study Group.

Parkinsonism Relat Disord. 2012 Jun;18(5):557-61. doi: 10.1016/j.parkreldis.2012.02.016. Epub 2012 Mar 17.

PMID:
22425546
3.

The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.

Tan EK, Zhao Y, Skipper L, Tan MG, Di Fonzo A, Sun L, Fook-Chong S, Tang S, Chua E, Yuen Y, Tan L, Pavanni R, Wong MC, Kolatkar P, Lu CS, Bonifati V, Liu JJ.

Hum Genet. 2007 Feb;120(6):857-63. Epub 2006 Sep 30.

PMID:
17019612
4.

The LRRK2 G2385R variant is a risk factor for sporadic Parkinson's disease in the Korean population.

Kim JM, Lee JY, Kim HJ, Kim JS, Shin ES, Cho JH, Park SS, Jeon BS.

Parkinsonism Relat Disord. 2010 Feb;16(2):85-8. doi: 10.1016/j.parkreldis.2009.10.004. Epub 2009 Oct 23.

PMID:
19854095
5.

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.

An XK, Peng R, Li T, Burgunder JM, Wu Y, Chen WJ, Zhang JH, Wang YC, Xu YM, Gou YR, Yuan GG, Zhang ZJ.

Eur J Neurol. 2008 Mar;15(3):301-5. doi: 10.1111/j.1468-1331.2007.02052.x. Epub 2008 Jan 14.

PMID:
18201193
6.

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 15;22(12):1816-8.

PMID:
17659642
7.

Analysis of the LRRK2 Gly2385Arg variant in Alzheimer's disease in Taiwan.

Chang TY, Kuo HC, Lu CS, Wu-Chou YH, Huang CC.

Parkinsonism Relat Disord. 2010 Jan;16(1):28-30. doi: 10.1016/j.parkreldis.2009.06.009. Epub 2009 Jul 28.

PMID:
19640773
8.

A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan.

Di Fonzo A, Wu-Chou YH, Lu CS, van Doeselaar M, Simons EJ, Rohé CF, Chang HC, Chen RS, Weng YH, Vanacore N, Breedveld GJ, Oostra BA, Bonifati V.

Neurogenetics. 2006 Jul;7(3):133-8. Epub 2006 Apr 22.

PMID:
16633828
9.

Lack of association between BST1 polymorphisms and sporadic Parkinson's disease in a Japanese population.

Miyake Y, Tanaka K, Fukushima W, Kiyohara C, Sasaki S, Tsuboi Y, Yamada T, Oeda T, Shimada H, Kawamura N, Sakae N, Fukuyama H, Hirota Y, Nagai M; Fukuoka Kinki Parkinson's Disease Study Group.

J Neurol Sci. 2012 Dec 15;323(1-2):162-6. doi: 10.1016/j.jns.2012.09.008. Epub 2012 Sep 29.

PMID:
23026536
10.

Essential tremor and the common LRRK2 G2385R variant.

Tan EK, Lee J, Lim HQ, Yuen Y, Zhao Y.

Parkinsonism Relat Disord. 2008 Nov;14(7):569-71. doi: 10.1016/j.parkreldis.2007.12.003. Epub 2008 Mar 3.

PMID:
18316234
11.

Case control analysis of LRRK2 Gly2385Arg in Alzheimer's disease.

Tan EK, Lee J, Chen CP, Wong MC, Zhao Y.

Neurobiol Aging. 2009 Mar;30(3):501-2. Epub 2007 Aug 27.

PMID:
17720280
12.

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. doi: 10.1016/j.parkreldis.2008.06.009. Epub 2008 Sep 20.

PMID:
18805725
13.

UCHL1 S18Y variant is a risk factor for Parkinson's disease in Japan.

Miyake Y, Tanaka K, Fukushima W, Kiyohara C, Sasaki S, Tsuboi Y, Yamada T, Oeda T, Shimada H, Kawamura N, Sakae N, Fukuyama H, Hirota Y, Nagai M; Fukuoka Kinki Parkinson’s Disease Study Group.

BMC Neurol. 2012 Jul 28;12:62. doi: 10.1186/1471-2377-12-62.

14.

Confirmation of LRRK2 S1647T variant as a risk factor for Parkinson's disease in southern China.

Zheng Y, Liu Y, Wu Q, Hong H, Zhou H, Chen J, Wang H, Xian W, Li J, Liu Z, Pei Z, Chen L.

Eur J Neurol. 2011 Mar;18(3):538-40. doi: 10.1111/j.1468-1331.2010.03164.x.

PMID:
20629711
15.

Brain-derived neurotrophic factor (BDNF) genetic polymorphism greatly increases risk of leucine-rich repeat kinase 2 (LRRK2) for Parkinson's disease.

Liu J, Zhou Y, Wang C, Wang T, Zheng Z, Chan P.

Parkinsonism Relat Disord. 2012 Feb;18(2):140-3. doi: 10.1016/j.parkreldis.2011.09.002. Epub 2011 Sep 16.

PMID:
21924942
16.

LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.

Zhang Z, Burgunder JM, An X, Wu Y, Chen W, Zhang J, Wang Y, Xu Y, Gou Y, Yuan G, Mao X, Peng R.

Mov Disord. 2009 Oct 15;24(13):1902-5. doi: 10.1002/mds.22371.

PMID:
19672984
17.

The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease.

Li C, Ting Z, Qin X, Ying W, Li B, Guo Qiang L, Jian Fang M, Jing Z, Jian Qing D, Sheng Di C.

Mov Disord. 2007 Dec;22(16):2439-43.

PMID:
17960808
18.

The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population.

Lu CS, Wu-Chou YH, van Doeselaar M, Simons EJ, Chang HC, Breedveld GJ, Di Fonzo A, Chen RS, Weng YH, Lai SC, Oostra BA, Bonifati V.

Neurogenetics. 2008 Oct;9(4):271-6. doi: 10.1007/s10048-008-0140-6. Epub 2008 Aug 21.

PMID:
18716801
19.

LRRK2 P755L variant in sporadic Parkinson's disease.

Tomiyama H, Mizuta I, Li Y, Funayama M, Yoshino H, Li L, Murata M, Yamamoto M, Kubo S, Mizuno Y, Toda T, Hattori N.

J Hum Genet. 2008;53(11-12):1012-5. doi: 10.1007/s10038-008-0336-5. Epub 2008 Oct 16.

PMID:
18923807
20.

GWAS-linked GAK locus in Parkinson's disease in Han Chinese and meta-analysis.

Li NN, Chang XL, Mao XY, Zhang JH, Zhao DM, Tan EK, Peng R.

Hum Genet. 2012 Jul;131(7):1089-93. doi: 10.1007/s00439-011-1133-3. Epub 2011 Dec 24.

PMID:
22198721
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