444 related articles for article (PubMed ID: 18704525)
1. 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]
2. 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]
3. 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]
4. 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]
5. Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements.
Scarciolla O; Brancati F; Valente EM; Ferraris A; De Angelis MV; Valbonesi S; Garavaglia B; Uncini A; Palka G; Stuppia L; Dallapiccola B
Mov Disord; 2007 Nov; 22(15):2274-8. PubMed ID: 17914726
[TBL] [Abstract][Full Text] [Related]
6. Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease.
Kilarski LL; Pearson JP; Newsway V; Majounie E; Knipe MD; Misbahuddin A; Chinnery PF; Burn DJ; Clarke CE; Marion MH; Lewthwaite AJ; Nicholl DJ; Wood NW; Morrison KE; Williams-Gray CH; Evans JR; Sawcer SJ; Barker RA; Wickremaratchi MM; Ben-Shlomo Y; Williams NM; Morris HR
Mov Disord; 2012 Oct; 27(12):1522-9. PubMed ID: 22956510
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.
Camargos ST; Dornas LO; Momeni P; Lees A; Hardy J; Singleton A; Cardoso F
Mov Disord; 2009 Apr; 24(5):662-6. PubMed ID: 19205068
[TBL] [Abstract][Full Text] [Related]
9. Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.
Nuytemans K; Meeus B; Crosiers D; Brouwers N; Goossens D; Engelborghs S; Pals P; Pickut B; Van den Broeck M; Corsmit E; Cras P; De Deyn PP; Del-Favero J; Van Broeckhoven C; Theuns J
Hum Mutat; 2009 Jul; 30(7):1054-61. PubMed ID: 19405094
[TBL] [Abstract][Full Text] [Related]
10. Mutation analysis of the PARKIN, PINK1, DJ1, and SNCA genes in Turkish early-onset Parkinson's patients and genotype-phenotype correlations.
Erer S; Egeli U; Zarifoglu M; Tezcan G; Cecener G; Tunca B; Ak S; Demirdogen E; Kenangil G; Kaleagası H; Dogu O; Saka E; Elibol B
Clin Neurol Neurosurg; 2016 Sep; 148():147-53. PubMed ID: 27455133
[TBL] [Abstract][Full Text] [Related]
11. Analysis of the genetic variability in Parkinson's disease from Southern Spain.
Bandrés-Ciga S; Mencacci NE; Durán R; Barrero FJ; Escamilla-Sevilla F; Morgan S; Hehir J; Vives F; Hardy J; Pittman AM
Neurobiol Aging; 2016 Jan; 37():210.e1-210.e5. PubMed ID: 26518746
[TBL] [Abstract][Full Text] [Related]
12. LRRK2 gene in Parkinson disease: mutation analysis and case control association study.
Paisán-Ruíz C; Lang AE; Kawarai T; Sato C; Salehi-Rad S; Fisman GK; Al-Khairallah T; St George-Hyslop P; Singleton A; Rogaeva E
Neurology; 2005 Sep; 65(5):696-700. PubMed ID: 16157901
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.
Nuytemans K; Theuns J; Cruts M; Van Broeckhoven C
Hum Mutat; 2010 Jul; 31(7):763-80. PubMed ID: 20506312
[TBL] [Abstract][Full Text] [Related]
16. Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease.
Benitez BA; Davis AA; Jin SC; Ibanez L; Ortega-Cubero S; Pastor P; Choi J; Cooper B; Perlmutter JS; Cruchaga C
Mol Neurodegener; 2016 Apr; 11():29. PubMed ID: 27094865
[TBL] [Abstract][Full Text] [Related]
17. Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2.
Bras J; Guerreiro R; Ribeiro M; Morgadinho A; Januario C; Dias M; Calado A; Semedo C; Oliveira C; Hardy J; Singleton A
BMC Neurol; 2008 Jan; 8():1. PubMed ID: 18211709
[TBL] [Abstract][Full Text] [Related]
18. Analysis of Exon Dosage Using Multiplex Ligation-Dependent Probe Amplification in Chinese Patients with Early-Onset Parkinson's Disease.
Lin Y; Zeng YF; Cai NQ; Lin XZ; Wang N; He J
Eur Neurol; 2019; 81(5-6):246-253. PubMed ID: 31618739
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Pathogenic mutations in Parkinson disease.
Tan EK; Skipper LM
Hum Mutat; 2007 Jul; 28(7):641-53. PubMed ID: 17385668
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]