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Results: 1 to 20 of 102

1.

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. doi: 10.1002/gcc.21995. Epub 2012 Aug 24.

PMID:
22927236
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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. doi: 10.1001/archneurol.2010.95.

PMID:
20558392
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

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. doi: 10.1017/S1355617710001190. Epub 2010 Nov 24.

PMID:
21092386
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

[Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].

Hattori N.

Rinsho Shinkeigaku. 2004 Apr-May;44(4-5):241-62. Review. Japanese.

PMID:
15287506
[PubMed - indexed for MEDLINE]
5.

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 15;129A(1):44-50. Erratum in: Am J Med Genet A. 2005 Nov 15;139(1):56.

PMID:
15266615
[PubMed - indexed for MEDLINE]
6.

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.

PMID:
16606767
[PubMed - indexed for MEDLINE]
7.

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 3;430(1):18-22.

PMID:
18068301
[PubMed - indexed for MEDLINE]
8.

Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control.

Brooks J, Ding J, Simon-Sanchez J, Paisan-Ruiz C, Singleton AB, Scholz SW.

J Med Genet. 2009 Jun;46(6):375-81. doi: 10.1136/jmg.2008.063917. Epub 2009 Apr 6.

PMID:
19351622
[PubMed - indexed for MEDLINE]
9.

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.

Abbas N, Lücking CB, Ricard S, Dürr A, Bonifati V, De Michele G, Bouley S, Vaughan JR, Gasser T, Marconi R, Broussolle E, Brefel-Courbon C, Harhangi BS, Oostra BA, Fabrizio E, Böhme GA, Pradier L, Wood NW, Filla A, Meco G, Denefle P, Agid Y, Brice A.

Hum Mol Genet. 1999 Apr;8(4):567-74.

PMID:
10072423
[PubMed - indexed for MEDLINE]
Free Article
10.

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.

PMID:
20424582
[PubMed - indexed for MEDLINE]
11.

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 15;22(7):932-7.

PMID:
17415800
[PubMed - indexed for MEDLINE]
12.

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.

PMID:
16476817
[PubMed - indexed for MEDLINE]
13.

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; French Parkinson's Disease Genetics Study Group.

Neurology. 2009 Jan 13;72(2):110-6. doi: 10.1212/01.wnl.0000327098.86861.d4. Epub 2008 Nov 5.

PMID:
18987353
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Association between early-onset Parkinson's disease and mutations in the parkin gene.

Lücking CB, Dürr A, Bonifati V, Vaughan J, De Michele G, Gasser T, Harhangi BS, Meco G, Denèfle P, Wood NW, Agid Y, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.

N Engl J Med. 2000 May 25;342(21):1560-7.

PMID:
10824074
[PubMed - indexed for MEDLINE]
Free Article
15.

Mutation screening and association analysis of the parkin gene in Parkinson's disease patients from South-West China.

Peng R, Gou Y, Yuan Q, Li T, Latsoudis H, Yuan G, Luo D, Liu X, Collier DA.

Eur Neurol. 2003;49(2):85-9.

PMID:
12584415
[PubMed - indexed for MEDLINE]
16.

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 14;477(1):19-22. doi: 10.1016/j.neulet.2010.04.026. Epub 2010 Apr 23.

PMID:
20399249
[PubMed - indexed for MEDLINE]
17.

Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism.

Myhre R, Steinkjer S, Stormyr A, Nilsen GL, Abu Zayyad H, Horany K, Nusier MK, Klungland H.

BMC Neurol. 2008 Dec 16;8:47. doi: 10.1186/1471-2377-8-47.

PMID:
19087301
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Genetic analysis of Parkin in early onset Parkinson's disease (PD): Novel intron 9 g > a single nucleotide polymorphism and risk of Taiwanese PD.

Wu YR, Wu CH, Chao CY, Kuan CC, Zhang WL, Wang CK, Chang CY, Chang YC, Lee-Chen GJ, Chen CM.

Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):229-34. doi: 10.1002/ajmg.b.30977.

PMID:
19475582
[PubMed - indexed for MEDLINE]
19.

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. doi: 10.1007/s00415-011-6110-1. Epub 2011 May 29.

PMID:
21625934
[PubMed - indexed for MEDLINE]
20.

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 28;1358:30-8. doi: 10.1016/j.brainres.2010.08.060. Epub 2010 Aug 26.

PMID:
20800584
[PubMed - indexed for MEDLINE]
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