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Items: 1 to 20 of 397

1.

Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore.

Lin CH, Tan EK, Chen ML, Tan LC, Lim HQ, Chen GS, Wu RM.

Neurology. 2008 Nov 18;71(21):1727-32. doi: 10.1212/01.wnl.0000335167.72412.68.

PMID:
19015489
2.

ATP13A2 variants in early-onset Parkinson's disease patients and controls.

Djarmati A, Hagenah J, Reetz K, Winkler S, Behrens MI, Pawlack H, Lohmann K, Ramirez A, Tadić V, Brüggemann N, Berg D, Siebner HR, Lang AE, Pramstaller PP, Binkofski F, Kostić VS, Volkmann J, Gasser T, Klein C.

Mov Disord. 2009 Oct 30;24(14):2104-11. doi: 10.1002/mds.22728.

PMID:
19705361
3.

Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China.

Fei QZ, Cao L, Xiao Q, Zhang T, Zheng L, Wang XJ, Wang G, Zhou HY, Wang Y, Chen SD.

Neurosci Lett. 2010 May 14;475(2):61-3. doi: 10.1016/j.neulet.2010.03.018. Epub 2010 Mar 19.

PMID:
20227461
4.

Rapid screening of ATP13A2 variant with high-resolution melting analysis.

Funayama M, Tomiyama H, Wu RM, Ogaki K, Yoshino H, Mizuno Y, Hattori N.

Mov Disord. 2010 Oct 30;25(14):2434-7. doi: 10.1002/mds.23106.

PMID:
20976737
5.

The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson's disease.

Chan AY, Baum L, Tang NL, Lau CY, Ng PW, Hui KF, Mizuno Y, Kwan JY, Mok VC, Kuo SH.

J Clin Neurosci. 2013 May;20(5):761-2. doi: 10.1016/j.jocn.2012.05.052. Epub 2013 Mar 20.

6.

ATP13A2 variability in Taiwanese Parkinson's disease.

Chen CM, Lin CH, Juan HF, Hu FJ, Hsiao YC, Chang HY, Chao CY, Chen IC, Lee LC, Wang TW, Chen YT, Chen YT, Lee-Chen GJ, Wu YR.

Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):720-9. doi: 10.1002/ajmg.b.31214. Epub 2011 Jun 28.

PMID:
21714071
7.

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
8.

Analysis of PArkin Co-Regulated Gene in a Taiwanese-ethnic Chinese cohort with early-onset Parkinson's disease.

Taylor JM, Wu RM, Farrer MJ, Delatycki MB, Lockhart PJ.

Parkinsonism Relat Disord. 2009 Jul;15(6):417-21. doi: 10.1016/j.parkreldis.2008.11.009. Epub 2009 Feb 3.

PMID:
19196541
9.

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
10.

Case-control study of the parkin gene in early-onset Parkinson disease.

Clark LN, Afridi S, Karlins E, Wang Y, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K.

Arch Neurol. 2006 Apr;63(4):548-52.

PMID:
16606767
11.

ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease.

Di Fonzo A, Chien HF, Socal M, Giraudo S, Tassorelli C, Iliceto G, Fabbrini G, Marconi R, Fincati E, Abbruzzese G, Marini P, Squitieri F, Horstink MW, Montagna P, Libera AD, Stocchi F, Goldwurm S, Ferreira JJ, Meco G, Martignoni E, Lopiano L, Jardim LB, Oostra BA, Barbosa ER; Italian Parkinson Genetics Network, Bonifati V.

Neurology. 2007 May 8;68(19):1557-62.

PMID:
17485642
12.

Genetic screening for mutations in the Nrdp1 gene in Parkinson disease patients in a Chinese population.

Mo X, Liu D, Li W, Hu Z, Hu Y, Li J, Guo J, Tang B, Zhang Z, Bai Y, Xia K.

Parkinsonism Relat Disord. 2010 Mar;16(3):222-4. doi: 10.1016/j.parkreldis.2009.09.001. Epub 2009 Oct 2.

PMID:
19800834
13.

[Mutation analysis of ATP13A2 gene in Chinese patients with familial autosomal recessive early-onset parkinsonism].

He D, Guo JF, Wang L, Xiao ZQ, Nie LL, Zhang XW, Tang BS.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):567-70. doi: 10.3760/cma.j.issn.1003-9406.2009.05.020. Chinese.

PMID:
19806583
14.

Mutational analysis of GIGYF2, ATP13A2 and GBA genes in Brazilian patients with early-onset Parkinson's disease.

Dos Santos AV, Pestana CP, Diniz KR, Campos M, Abdalla-Carvalho CB, de Rosso AL, Pereira JS, Nicaretta DH, de Carvalho WL, Dos Santos JM, Santos-Rebouças CB, Pimentel MM.

Neurosci Lett. 2010 Nov 19;485(2):121-4. doi: 10.1016/j.neulet.2010.08.083. Epub 2010 Sep 17.

PMID:
20816920
15.

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
16.

Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese population.

Wang L, Guo JF, Zhang WW, Xu Q, Zuo X, Shi CH, Luo LZ, Liu J, Hu L, Hu YC, She L, Jiang H, Yan XX, Xia K, Pan Q, Tang BS.

Neurosci Lett. 2010 Apr 5;473(2):131-5. doi: 10.1016/j.neulet.2010.02.037. Epub 2010 Feb 21.

PMID:
20178831
17.
18.

Association of mutations in the glucocerebrosidase gene with Parkinson disease in a Korean population.

Choi JM, Kim WC, Lyoo CH, Kang SY, Lee PH, Baik JS, Koh SB, Ma HI, Sohn YH, Lee MS, Kim YJ.

Neurosci Lett. 2012 Apr 11;514(1):12-5. doi: 10.1016/j.neulet.2012.02.035. Epub 2012 Feb 22.

PMID:
22387070
19.

Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.

Rakovic A, Stiller B, Djarmati A, Flaquer A, Freudenberg J, Toliat MR, Linnebank M, Kostic V, Lohmann K, Paus S, Nürnberg P, Kubisch C, Klein C, Wüllner U, Ramirez A.

Mov Disord. 2009 Feb 15;24(3):429-33. doi: 10.1002/mds.22399.

PMID:
19097176
20.

parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease.

Poorkaj P, Nutt JG, James D, Gancher S, Bird TD, Steinbart E, Schellenberg GD, Payami H.

Am J Med Genet A. 2004 Aug 15;129A(1):44-50. Erratum in: Am J Med Genet A. 2005 Nov 15;139(1):56.

PMID:
15266615
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