167 related articles for article (PubMed ID: 21092386)
1. Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study.
Caccappolo E; Alcalay RN; Mejia-Santana H; Tang MX; Rakitin B; Rosado L; Louis ED; Comella CL; Colcher A; Jennings D; Nance MA; Bressman S; Scott WK; Tanner CM; Mickel SF; Andrews HF; Waters C; Fahn S; Cote LJ; Frucht S; Ford B; Rezak M; Novak K; Friedman JH; Pfeiffer RF; Marsh L; Hiner B; Siderowf AD; Ross BM; Verbitsky M; Kisselev S; Ottman R; Clark LN; Marder KS
J Int Neuropsychol Soc; 2011 Jan; 17(1):91-100. PubMed ID: 21092386
[TBL] [Abstract][Full Text] [Related]
2. The relation between depression and parkin genotype: the CORE-PD study.
Srivastava A; Tang MX; Mejia-Santana H; Rosado L; Louis ED; Caccappolo E; Comella C; Colcher A; Siderowf A; Jennings D; Nance M; Bressman S; Scott WK; Tanner C; Mickel S; Andrews H; Waters C; Fahn S; Cote L; Frucht S; Ford B; Alcalay RN; Ross B; Orbe Reilly M; Rezak M; Novak K; Friedman JH; Pfeiffer RD; Marsh L; Hiner B; Merle D; Ottman R; Clark LN; Marder K
Parkinsonism Relat Disord; 2011 Dec; 17(10):740-4. PubMed ID: 21856206
[TBL] [Abstract][Full Text] [Related]
3. Olfaction in Parkin single and compound heterozygotes in a cohort of young onset Parkinson's disease patients.
Malek N; Swallow DM; Grosset KA; Lawton MA; Smith CR; Bajaj NP; Barker RA; Ben-Shlomo Y; Bresner C; Burn DJ; Foltynie T; Morris HR; Williams N; Wood NW; Grosset DG;
Acta Neurol Scand; 2016 Oct; 134(4):271-6. PubMed ID: 26626018
[TBL] [Abstract][Full Text] [Related]
4. A multidisciplinary study of patients with early-onset PD with and without parkin mutations.
Lohmann E; Thobois S; Lesage S; Broussolle E; du Montcel ST; Ribeiro MJ; Remy P; Pelissolo A; Dubois B; Mallet L; Pollak P; Agid Y; Brice A;
Neurology; 2009 Jan; 72(2):110-6. PubMed ID: 18987353
[TBL] [Abstract][Full Text] [Related]
5. Olfaction in Parkin heterozygotes and compound heterozygotes: the CORE-PD study.
Alcalay RN; Siderowf A; Ottman R; Caccappolo E; Mejia-Santana H; Tang MX; Rosado L; Louis E; Ruiz D; Waters C; Fahn S; Cote L; Frucht S; Ford B; Orbe-Reilly M; Ross B; Verbitsky M; Kisselev S; Comella C; Colcher A; Jennings D; Nance M; Bressman S; Scott WK; Tanner C; Mickel S; Rezak M; Novak KE; Friedman JH; Pfeiffer R; Marsh L; Hiner B; Clark LN; Marder K
Neurology; 2011 Jan; 76(4):319-26. PubMed ID: 21205674
[TBL] [Abstract][Full Text] [Related]
6. The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.
Sharp ME; Caccappolo E; Mejia-Santana H; Tang MX; Rosado L; Orbe Reilly M; Ruiz D; Louis ED; Comella C; Nance M; Bressman S; Scott WK; Tanner C; Waters C; Fahn S; Cote L; Ford B; Rezak M; Novak K; Friedman JH; Pfeiffer R; Payami H; Molho E; Factor SA; Nutt J; Serrano C; Arroyo M; Pauciulo MW; Nichols WC; Clark LN; Alcalay RN; Marder KS
Mov Disord; 2015 Feb; 30(2):278-83. PubMed ID: 25393808
[TBL] [Abstract][Full Text] [Related]
7. Eye movement disorders are different in Parkin-linked and idiopathic early-onset PD.
Machner B; Klein C; Sprenger A; Baumbach P; Pramstaller PP; Helmchen C; Heide W
Neurology; 2010 Jul; 75(2):125-8. PubMed ID: 20625164
[TBL] [Abstract][Full Text] [Related]
8. Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD study.
Alcalay RN; Caccappolo E; Mejia-Santana H; Tang M-; Rosado L; Orbe Reilly M; Ruiz D; Ross B; Verbitsky M; Kisselev S; Louis E; Comella C; Colcher A; Jennings D; Nance M; Bressman S; Scott WK; Tanner C; Mickel S; Andrews H; Waters C; Fahn S; Cote L; Frucht S; Ford B; Rezak M; Novak K; Friedman JH; Pfeiffer R; Marsh L; Hiner B; Siderowf A; Payami H; Molho E; Factor S; Ottman R; Clark LN; Marder K
Neurology; 2012 May; 78(18):1434-40. PubMed ID: 22442429
[TBL] [Abstract][Full Text] [Related]
9. Non-motor Symptoms in Parkinson's Disease Patients with Parkin Mutations: More Depression and Less Executive Dysfunction.
Song J; Shen B; Yang YJ; Liu FT; Zhao J; Tang YL; Chen C; Ding ZT; An Y; Wu JJ; Sun YM; Wang J
J Mol Neurosci; 2020 Feb; 70(2):246-253. PubMed ID: 31927768
[TBL] [Abstract][Full Text] [Related]
10. Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study.
Marder KS; Tang MX; Mejia-Santana H; Rosado L; Louis ED; Comella CL; Colcher A; Siderowf AD; Jennings D; Nance MA; Bressman S; Scott WK; Tanner CM; Mickel SF; Andrews HF; Waters C; Fahn S; Ross BM; Cote LJ; Frucht S; Ford B; Alcalay RN; Rezak M; Novak K; Friedman JH; Pfeiffer RF; Marsh L; Hiner B; Neils GD; Verbitsky M; Kisselev S; Caccappolo E; Ottman R; Clark LN
Arch Neurol; 2010 Jun; 67(6):731-8. PubMed ID: 20558392
[TBL] [Abstract][Full Text] [Related]
11. Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson's disease: contribution of automated segmentation neuroimaging method.
Bilgic B; Bayram A; Arslan AB; Hanagasi H; Dursun B; Gurvit H; Emre M; Lohmann E
Parkinsonism Relat Disord; 2012 Jun; 18(5):562-6. PubMed ID: 22445249
[TBL] [Abstract][Full Text] [Related]
12. Cognitive and motor function in long-duration PARKIN-associated Parkinson disease.
Alcalay RN; Caccappolo E; Mejia-Santana H; Tang MX; Rosado L; Orbe Reilly M; Ruiz D; Louis ED; Comella CL; Nance MA; Bressman SB; Scott WK; Tanner CM; Mickel SF; Waters CH; Fahn S; Cote LJ; Frucht SJ; Ford B; Rezak M; Novak KE; Friedman JH; Pfeiffer RF; Marsh L; Hiner B; Payami H; Molho E; Factor SA; Nutt JG; Serrano C; Arroyo M; Ottman R; Pauciulo MW; Nichols WC; Clark LN; Marder KS
JAMA Neurol; 2014 Jan; 71(1):62-7. PubMed ID: 24190026
[TBL] [Abstract][Full Text] [Related]
13. Language Deficits as a Preclinical Window into Parkinson's Disease: Evidence from Asymptomatic Parkin and Dardarin Mutation Carriers.
García AM; Sedeño L; Trujillo N; Bocanegra Y; Gomez D; Pineda D; Villegas A; Muñoz E; Arias W; Ibáñez A
J Int Neuropsychol Soc; 2017 Feb; 23(2):150-158. PubMed ID: 28205494
[TBL] [Abstract][Full Text] [Related]
14. Disease Progression in Patients with Parkin-Related Parkinson's Disease in a Longitudinal Cohort.
Sun YM; Yu HL; Zhou XY; Xiong WX; Luo SS; Chen C; Liu FT; Zhao J; Tang YL; Liang XN; Yang YJ; Shen B; Shen Y; Yu WB; Ding ZT; An Y; Wu JJ; Wang J
Mov Disord; 2021 Feb; 36(2):442-448. PubMed ID: 33107659
[TBL] [Abstract][Full Text] [Related]
15. Event-related potential changes due to early-onset Parkinson's disease in parkin (PARK2) gene mutation carriers and non-carriers.
Uslu A; Ergen M; Demirci H; Lohmann E; Hanagasi H; Demiralp T
Clin Neurophysiol; 2020 Jul; 131(7):1444-1452. PubMed ID: 32388155
[TBL] [Abstract][Full Text] [Related]
16. Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene.
Clark LN; Haamer E; Mejia-Santana H; Harris J; Lesage S; Durr A; Bs SJ; Hedrich K; Louis ED; Cote LJ; Andrews H; Fahn S; Waters C; Ford B; Frucht S; Scott W; Klein C; Brice A; Roomere H; Ottman R; Marder K
Mov Disord; 2007 May; 22(7):932-7. PubMed ID: 17415800
[TBL] [Abstract][Full Text] [Related]
17. Phenotype analysis in patients with early onset Parkinson's disease with and without parkin mutations.
Kim HJ; Kim HJ; Lee JY; Yun JY; Kim SY; Park SS; Jeon BS
J Neurol; 2011 Dec; 258(12):2260-7. PubMed ID: 21625934
[TBL] [Abstract][Full Text] [Related]
18. Lack of association between cancer history and PARKIN genotype: a family based study in PARKIN/Parkinson's families.
Alcalay RN; Clark LN; Marder KS; Bradley WE
Genes Chromosomes Cancer; 2012 Dec; 51(12):1109-13. PubMed ID: 22927236
[TBL] [Abstract][Full Text] [Related]
19. Parkin mutations and phenotypic features in Czech patients with early-onset Parkinson's disease.
Fiala O; Pospisilova L; Prochazkova J; Matejckova M; Martasek P; Novakova L; Roth J; Ruzicka E
Neuro Endocrinol Lett; 2010; 31(2):187-92. PubMed ID: 20424582
[TBL] [Abstract][Full Text] [Related]
20. Mutation analysis of parkin and PINK1 genes in early-onset Parkinson's disease in China.
Zhang BR; Hu ZX; Yin XZ; Cai M; Zhao GH; Liu ZR; Luo W
Neurosci Lett; 2010 Jun; 477(1):19-22. PubMed ID: 20399249
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]