These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 21856206)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 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 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]  

  • 6. Mutation analysis of the parkin and PINK1 genes in American Caucasian early-onset Parkinson disease families.
    Deng H; Le W; Shahed J; Xie W; Jankovic J
    Neurosci Lett; 2008 Jan; 430(1):18-22. PubMed ID: 18068301
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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. PubMed ID: 16606767
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Heterogeneous phenotype in a family with compound heterozygous parkin gene mutations.
    Deng H; Le WD; Hunter CB; Ondo WG; Guo Y; Xie WJ; Jankovic J
    Arch Neurol; 2006 Feb; 63(2):273-7. PubMed ID: 16476817
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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; 129A(1):44-50. PubMed ID: 15266615
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.
    Sun M; Latourelle JC; Wooten GF; Lew MF; Klein C; Shill HA; Golbe LI; Mark MH; Racette BA; Perlmutter JS; Parsian A; Guttman M; Nicholson G; Xu G; Wilk JB; Saint-Hilaire MH; DeStefano AL; Prakash R; Williamson S; Suchowersky O; Labelle N; Growdon JH; Singer C; Watts RL; Goldwurm S; Pezzoli G; Baker KB; Pramstaller PP; Burn DJ; Chinnery PF; Sherman S; Vieregge P; Litvan I; Gillis T; MacDonald ME; Myers RH; Gusella JF
    Arch Neurol; 2006 Jun; 63(6):826-32. PubMed ID: 16769863
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rare and novel variants of PRKN and PINK1 genes in Vietnamese patients with early-onset Parkinson's disease.
    Ton ND; Thuan ND; Thuong MTH; Ngoc TTB; Nhung VP; Hoa NTT; Nam NH; Dung HT; Son ND; Ba NV; Bac ND; Tai TN; Dung LTK; Hung NT; Duong NT; Ha NH; Hai NV
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1463. PubMed ID: 32856414
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Parkin dosage mutations in patients with early-onset sporadic and familial Parkinson's disease in Chinese: an independent pathogenic role.
    Wang C; Ma H; Feng X; Xie S; Chan P
    Brain Res; 2010 Oct; 1358():30-8. PubMed ID: 20800584
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations.
    Pankratz N; Kissell DK; Pauciulo MW; Halter CA; Rudolph A; Pfeiffer RF; Marder KS; Foroud T; Nichols WC;
    Neurology; 2009 Jul; 73(4):279-86. PubMed ID: 19636047
    [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]
    of 9.