320 related articles for article (PubMed ID: 12953260)
1. The role of pathogenic DJ-1 mutations in Parkinson's disease.
Abou-Sleiman PM; Healy DG; Quinn N; Lees AJ; Wood NW
Ann Neurol; 2003 Sep; 54(3):283-6. PubMed ID: 12953260
[TBL] [Abstract][Full Text] [Related]
2. Genetic analysis of DJ-1 in a cohort Parkinson's disease patients of different ethnicity.
Tan EK; Tan C; Zhao Y; Yew K; Shen H; Chandran VR; Teoh ML; Yih Y; Pavanni R; Wong MC
Neurosci Lett; 2004 Aug; 367(1):109-12. PubMed ID: 15308309
[TBL] [Abstract][Full Text] [Related]
3. Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.
Clark LN; Afridi S; Mejia-Santana H; Harris J; Louis ED; Cote LJ; Andrews H; Singleton A; Wavrant De-Vrieze F; Hardy J; Mayeux R; Fahn S; Waters C; Ford B; Frucht S; Ottman R; Marder K
Mov Disord; 2004 Jul; 19(7):796-800. PubMed ID: 15254937
[TBL] [Abstract][Full Text] [Related]
4. DJ-1 mutations in Parkinson's disease.
Healy DG; Abou-Sleiman PM; Valente EM; Gilks WP; Bhatia K; Quinn N; Lees AJ; Wood NW
J Neurol Neurosurg Psychiatry; 2004 Jan; 75(1):144-5. PubMed ID: 14707326
[TBL] [Abstract][Full Text] [Related]
5. Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism.
Lockhart PJ; Bounds R; Hulihan M; Kachergus J; Lincoln S; Lin CH; Wu RM; Farrer MJ
Mov Disord; 2004 Sep; 19(9):1065-9. PubMed ID: 15372597
[TBL] [Abstract][Full Text] [Related]
6. DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.
Hedrich K; Djarmati A; Schäfer N; Hering R; Wellenbrock C; Weiss PH; Hilker R; Vieregge P; Ozelius LJ; Heutink P; Bonifati V; Schwinger E; Lang AE; Noth J; Bressman SB; Pramstaller PP; Riess O; Klein C
Neurology; 2004 Feb; 62(3):389-94. PubMed ID: 14872018
[TBL] [Abstract][Full Text] [Related]
7. Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients.
Koziorowski D; Hoffman-Zacharska D; Sławek J; Jamrozik Z; Janik P; Potulska-Chromik A; Roszmann A; Tataj R; Bal J; Friedman A
Neurol Neurochir Pol; 2013; 47(4):319-24. PubMed ID: 23986421
[TBL] [Abstract][Full Text] [Related]
8. Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease.
Macedo MG; Verbaan D; Fang Y; van Rooden SM; Visser M; Anar B; Uras A; Groen JL; Rizzu P; van Hilten JJ; Heutink P
Mov Disord; 2009 Jan; 24(2):196-203. PubMed ID: 18973254
[TBL] [Abstract][Full Text] [Related]
9. Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease.
Choi JM; Woo MS; Ma HI; Kang SY; Sung YH; Yong SW; Chung SJ; Kim JS; Shin HW; Lyoo CH; Lee PH; Baik JS; Kim SJ; Park MY; Sohn YH; Kim JH; Kim JW; Lee MS; Lee MC; Kim DH; Kim YJ
Neurogenetics; 2008 Oct; 9(4):263-9. PubMed ID: 18704525
[TBL] [Abstract][Full Text] [Related]
10. Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease.
Yonova-Doing E; Atadzhanov M; Quadri M; Kelly P; Shawa N; Musonda ST; Simons EJ; Breedveld GJ; Oostra BA; Bonifati V
Parkinsonism Relat Disord; 2012 Jun; 18(5):567-71. PubMed ID: 22445250
[TBL] [Abstract][Full Text] [Related]
11. Exon dosage variations in Brazilian patients with Parkinson's disease: analysis of SNCA, PARKIN, PINK1 and DJ-1 genes.
Moura KC; Junior MC; de Rosso AL; Nicaretta DH; Pereira JS; José Silva D; Santos-Rebouças CB; Pimentel MM
Dis Markers; 2012; 32(3):173-8. PubMed ID: 22377733
[TBL] [Abstract][Full Text] [Related]
12. Screening PARK genes for mutations in early-onset Parkinson's disease patients from Queensland, Australia.
Mellick GD; Siebert GA; Funayama M; Buchanan DD; Li Y; Imamichi Y; Yoshino H; Silburn PA; Hattori N
Parkinsonism Relat Disord; 2009 Feb; 15(2):105-9. PubMed ID: 18486522
[TBL] [Abstract][Full Text] [Related]
13. Evaluating intra-genetic variants of DJ-1 among Parkinson's disease patients of eastern India.
Sanyal J; Sarkar B; Banerjee TK; Mukherjee SC; Ray BC; Raghavendra Rao V
Neurol Res; 2011 May; 33(4):349-53. PubMed ID: 21535932
[TBL] [Abstract][Full Text] [Related]
14. PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations.
Ghazavi F; Fazlali Z; Banihosseini SS; Hosseini SR; Kazemi MH; Shojaee S; Parsa K; Sadeghi H; Sina F; Rohani M; Shahidi GA; Ghaemi N; Ronaghi M; Elahi E
Mov Disord; 2011 Jan; 26(1):80-9. PubMed ID: 21322020
[TBL] [Abstract][Full Text] [Related]
15. Mutation analysis for DJ-1 in sporadic and familial parkinsonism: screening strategy in parkinsonism.
Tomiyama H; Li Y; Yoshino H; Mizuno Y; Kubo S; Toda T; Hattori N
Neurosci Lett; 2009 May; 455(3):159-61. PubMed ID: 19429112
[TBL] [Abstract][Full Text] [Related]
16. Screening of two indel polymorphisms in the 5'UTR of the DJ-1 gene in South African Parkinson's disease patients.
Glanzmann B; Lombard D; Carr J; Bardien S
J Neural Transm (Vienna); 2014 Feb; 121(2):135-8. PubMed ID: 24052110
[TBL] [Abstract][Full Text] [Related]
17. Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD.
Eerola J; Hernandez D; Launes J; Hellström O; Hague S; Gulick C; Johnson J; Peuralinna T; Hardy J; Tienari PJ; Singleton AB
Neurology; 2003 Oct; 61(7):1000-2. PubMed ID: 14557580
[TBL] [Abstract][Full Text] [Related]
18. Mutations in DJ-1 are rare in familial Parkinson disease.
Pankratz N; Pauciulo MW; Elsaesser VE; Marek DK; Halter CA; Wojcieszek J; Rudolph A; Shults CW; Foroud T; Nichols WC;
Neurosci Lett; 2006 Nov; 408(3):209-13. PubMed ID: 16997464
[TBL] [Abstract][Full Text] [Related]
19. Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism.
Guo JF; Zhang XW; Nie LL; Zhang HN; Liao B; Li J; Wang L; Yan XX; Tang BS
J Neurol; 2010 Jul; 257(7):1170-5. PubMed ID: 20146068
[TBL] [Abstract][Full Text] [Related]
20. Causes of Parkinson's disease: genetics of DJ-1.
Abou-Sleiman PM; Healy DG; Wood NW
Cell Tissue Res; 2004 Oct; 318(1):185-8. PubMed ID: 15503154
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
