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Results: 1 to 20 of 118

1.

PARK2 gene mutations in early onset Parkinson's disease patients of South India.

Padmaja MV, Jayaraman M, Srinivasan AV, Srisailapathy CR, Ramesh A.

Neurosci Lett. 2012 Aug 15;523(2):145-7. doi: 10.1016/j.neulet.2012.06.062. Epub 2012 Jul 3.

PMID:
22766139
[PubMed - indexed for MEDLINE]
2.

Analysis of PARK2 gene exon rearrangements in Russian patients with sporadic Parkinson's disease.

Semenova EV, Shadrina MI, Slominsky PA, Ivanova-Smolenskaya IA, Bagyeva G, Illarioshkin SN, Limborska SA.

Mov Disord. 2012 Jan;27(1):139-42. doi: 10.1002/mds.23901. Epub 2011 Sep 13.

PMID:
21915905
[PubMed - indexed for MEDLINE]
3.

[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]
4.

Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease.

Madegowda RH, Kishore A, Anand A.

J Neurol Neurosurg Psychiatry. 2005 Nov;76(11):1588-90.

PMID:
16227559
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients.

Aguiar Pde C, Lessa PS, Godeiro C Jr, Barsottini O, Felício AC, Borges V, Silva SM, Saba RA, Ferraz HB, Moreira-Filho CA, Andrade LA.

Mov Disord. 2008 Jul 15;23(9):1228-33. doi: 10.1002/mds.22032.

PMID:
18464276
[PubMed - indexed for MEDLINE]
6.

Low frequency of the PARK2 gene mutations in Polish patients with the early-onset form of Parkinson disease.

Koziorowski D, Hoffman-Zacharska D, Sławek J, Szirkowiec W, Janik P, Bal J, Friedman A.

Parkinsonism Relat Disord. 2010 Feb;16(2):136-8. doi: 10.1016/j.parkreldis.2009.06.010. Epub 2009 Jul 22.

PMID:
19628420
[PubMed - indexed for MEDLINE]
7.

PARK2 mutations and clinical features in a Chinese population with early-onset Parkinson's disease.

Chan DK, Mok V, Ng PW, Yeung J, Kwok JB, Fang ZM, Clarke R, Wong L, Schofield PR, Hattori N.

J Neural Transm. 2008 May;115(5):715-9. doi: 10.1007/s00702-007-0011-6. Epub 2008 Jan 11.

PMID:
18188499
[PubMed - indexed for MEDLINE]
8.

Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease.

Hertz JM, Ostergaard K, Juncker I, Pedersen S, Romstad A, Møller LB, Güttler F, Dupont E.

Eur J Neurol. 2006 Apr;13(4):385-90.

PMID:
16643317
[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.

Occurrence of PARK2 mutations in a never-smoker population with Parkinson's disease in North India.

Prabhakar S, Vinish M, Das CP, Anand A.

Neuroepidemiology. 2010 Aug;35(2):152-9. doi: 10.1159/000313855. Epub 2010 Jun 23.

PMID:
20571283
[PubMed - indexed for MEDLINE]
11.

Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients.

Koziorowski D, Hoffman-Zacharska D, Sławek J, Jamrozik Z, Janik P, Potulska-Chromik A, Roszmann A, Tataj R, Bal J, Friedman A.

Neurol Neurochir Pol. 2013 Jul-Aug;47(4):319-24.

PMID:
23986421
[PubMed - indexed for MEDLINE]
12.

PARK2 variability in Polish Parkinson's disease patients--interaction with mitochondrial haplogroups.

Gaweda-Walerych K, Safranow K, Jasinska-Myga B, Bialecka M, Klodowska-Duda G, Rudzinska M, Czyzewski K, Cobb SA, Slawek J, Styczynska M, Opala G, Drozdzik M, Nishioka K, Farrer MJ, Ross OA, Wszolek ZK, Barcikowska M, Zekanowski C.

Parkinsonism Relat Disord. 2012 Jun;18(5):520-4. doi: 10.1016/j.parkreldis.2012.01.021. Epub 2012 Feb 22.

PMID:
22361577
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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.

PMID:
16769863
[PubMed - indexed for MEDLINE]
14.

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]
15.

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]
16.

Genetic analysis of PARK2 and PINK1 genes in Brazilian patients with early-onset Parkinson's disease.

Moura KC, Campos Junior M, de Rosso AL, Nicaretta DH, Pereira JS, Silva DJ, dos Santos FL, Rodrigues Fda C, Santos-Rebouças CB, Pimentel MM.

Dis Markers. 2013;35(3):181-5. doi: 10.1155/2013/597158. Epub 2013 Aug 14.

PMID:
24167364
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Phase analysis identifies compound heterozygous deletions of the PARK2 gene in patients with early-onset Parkinson disease.

Kim SY, Seong MW, Jeon BS, Kim SY, Ko HS, Kim JY, Park SS.

Clin Genet. 2012 Jul;82(1):77-82. doi: 10.1111/j.1399-0004.2011.01693.x. Epub 2011 May 29.

PMID:
21534944
[PubMed - indexed for MEDLINE]
18.

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]
19.

A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2.

Kay DM, Stevens CF, Hamza TH, Montimurro JS, Zabetian CP, Factor SA, Samii A, Griffith A, Roberts JW, Molho ES, Higgins DS, Gancher S, Moses L, Zareparsi S, Poorkaj P, Bird T, Nutt J, Schellenberg GD, Payami H.

Neurology. 2010 Sep 28;75(13):1189-94. doi: 10.1212/WNL.0b013e3181f4d832.

PMID:
20876472
[PubMed - indexed for MEDLINE]
Free PMC Article
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 14;477(1):19-22. doi: 10.1016/j.neulet.2010.04.026. Epub 2010 Apr 23.

PMID:
20399249
[PubMed - indexed for MEDLINE]

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