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Results: 1 to 20 of 88

1.

Primary progressive multiple sclerosis developing in the context of young onset Parkinson's disease.

Sadnicka A, Sheerin UM, Kaplan C, Molloy S, Muraro PA.

Mult Scler. 2013 Jan;19(1):123-5. doi: 10.1177/1352458512445942. Epub 2012 Apr 20.

PMID:
22523156
[PubMed - indexed for MEDLINE]
2.

[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]
3.

Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil.

Chien HF, Rohé CF, Costa MD, Breedveld GJ, Oostra BA, Barbosa ER, Bonifati V.

Neurogenetics. 2006 Mar;7(1):13-9. Epub 2005 Nov 22.

PMID:
16328510
[PubMed - indexed for MEDLINE]
4.

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. doi: 10.1016/j.parkreldis.2012.02.017. Epub 2012 Mar 24.

PMID:
22445249
[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.

Onset and progression of disease in familial and sporadic Parkinson's disease.

Inzelberg R, Schecthman E, Paleacu D, Zach L, Bonwitt R, Carasso RL, Nisipeanu P.

Am J Med Genet A. 2004 Jan 30;124A(3):255-8.

PMID:
14708097
[PubMed - indexed for MEDLINE]
7.

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]
8.

Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers.

Pramstaller PP, Schlossmacher MG, Jacques TS, Scaravilli F, Eskelson C, Pepivani I, Hedrich K, Adel S, Gonzales-McNeal M, Hilker R, Kramer PL, Klein C.

Ann Neurol. 2005 Sep;58(3):411-22.

PMID:
16130111
[PubMed - indexed for MEDLINE]
9.

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]
10.

Parkin polymorphisms and environmental exposure: decrease in age at onset of Parkinson's disease.

Ghione I, Di Fonzo A, Saladino F, Del Bo R, Bresolin N, Comi GP, Rango M.

Neurotoxicology. 2007 May;28(3):698-701. Epub 2007 Jan 20.

PMID:
17335904
[PubMed - indexed for MEDLINE]
11.

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]
13.

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]
14.

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
15.

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]
16.

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]
17.

Molecular pathogenesis of Parkinson's disease: identification of mutations in the Parkin gene in Indian patients.

Biswas A, Gupta A, Naiya T, Das G, Neogi R, Datta S, Mukherjee S, Das SK, Ray K, Ray J.

Parkinsonism Relat Disord. 2006 Oct;12(7):420-6. Epub 2006 Jun 21.

PMID:
16793319
[PubMed - indexed for MEDLINE]
18.

Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease.

Sinha R, Racette B, Perlmutter JS, Parsian A.

Parkinsonism Relat Disord. 2005 Sep;11(6):341-7.

PMID:
16019250
[PubMed - indexed for MEDLINE]
19.

Parkinson's disease in Ireland: clinical presentation and genetic heterogeneity in patients with parkin mutations.

Wiley J, Lynch T, Lincoln S, Skipper L, Hulihan M, Gosal D, Bisceglio G, Kachergus J, Hardy J, Farrer MJ.

Mov Disord. 2004 Jun;19(6):677-81.

PMID:
15197707
[PubMed - indexed for MEDLINE]
20.

Parkin gene variations in late-onset Parkinson's disease: comparison between Norwegian and German cohorts.

Schlitter AM, Kurz M, Larsen JP, Woitalla D, Müller T, Epplen JT, Dekomien G.

Acta Neurol Scand. 2006 Jan;113(1):9-13.

PMID:
16367892
[PubMed - indexed for MEDLINE]

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