235 related articles for article (PubMed ID: 30584170)
1. MDSGene: Closing Data Gaps in Genotype-Phenotype Correlations of Monogenic Parkinson's Disease.
Klein C; Hattori N; Marras C
J Parkinsons Dis; 2018; 8(s1):S25-S30. PubMed ID: 30584170
[TBL] [Abstract][Full Text] [Related]
2. Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review.
Trinh J; Zeldenrust FMJ; Huang J; Kasten M; Schaake S; Petkovic S; Madoev H; Grünewald A; Almuammar S; König IR; Lill CM; Lohmann K; Klein C; Marras C
Mov Disord; 2018 Dec; 33(12):1857-1870. PubMed ID: 30357936
[TBL] [Abstract][Full Text] [Related]
3. Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic Review.
Kasten M; Hartmann C; Hampf J; Schaake S; Westenberger A; Vollstedt EJ; Balck A; Domingo A; Vulinovic F; Dulovic M; Zorn I; Madoev H; Zehnle H; Lembeck CM; Schawe L; Reginold J; Huang J; König IR; Bertram L; Marras C; Lohmann K; Lill CM; Klein C
Mov Disord; 2018 May; 33(5):730-741. PubMed ID: 29644727
[TBL] [Abstract][Full Text] [Related]
4. Therapies for Genetic Forms of Parkinson's Disease: Systematic Literature Review.
Over L; Brüggemann N; Lohmann K
J Neuromuscul Dis; 2021; 8(3):341-356. PubMed ID: 33459660
[TBL] [Abstract][Full Text] [Related]
5. Genotype-Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic Review.
Wittke C; Petkovic S; Dobricic V; Schaake S; ; Respondek G; Weissbach A; Madoev H; Trinh J; Vollstedt EJ; Kuhnke N; Lohmann K; Dulovic Mahlow M; Marras C; König IR; Stamelou M; Bonifati V; Lill CM; Kasten M; Huppertz HJ; Höglinger G; Klein C
Mov Disord; 2021 Jul; 36(7):1499-1510. PubMed ID: 34396589
[TBL] [Abstract][Full Text] [Related]
6. 'Atypical' Parkinson's disease - genetic.
Weissbach A; Wittke C; Kasten M; Klein C
Int Rev Neurobiol; 2019; 149():207-235. PubMed ID: 31779813
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Genetics of Parkinson disease.
Domingo A; Klein C
Handb Clin Neurol; 2018; 147():211-227. PubMed ID: 29325612
[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 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]
11. 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]
12. Structural genomic variations and Parkinson's disease.
Bandrés-Ciga S; Ruz C; Barrero FJ; Escamilla-Sevilla F; Pelegrina J; Vives F; Duran R
Minerva Med; 2017 Oct; 108(5):438-447. PubMed ID: 28541025
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Genetic variants of PARK genes in Korean patients with early-onset Parkinson's disease.
Youn J; Lee C; Oh E; Park J; Kim JS; Kim HT; Cho JW; Park WY; Jang W; Ki CS
Neurobiol Aging; 2019 Mar; 75():224.e9-224.e15. PubMed ID: 30502028
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Genetics and epigenetics of Parkinson's disease.
Coppedè F
ScientificWorldJournal; 2012; 2012():489830. PubMed ID: 22623900
[TBL] [Abstract][Full Text] [Related]
17. Impact of recent genetic findings in Parkinson's disease.
Klein C; Lohmann-Hedrich K
Curr Opin Neurol; 2007 Aug; 20(4):453-64. PubMed ID: 17620882
[TBL] [Abstract][Full Text] [Related]
18. Nonmotor Signs in Genetic Forms of Parkinson's Disease.
Kasten M; Marras C; Klein C
Int Rev Neurobiol; 2017; 133():129-178. PubMed ID: 28802919
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. The curious case of phenocopies in families with genetic Parkinson's disease.
Klein C; Chuang R; Marras C; Lang AE
Mov Disord; 2011 Aug; 26(10):1793-802. PubMed ID: 21735483
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
