353 related articles for article (PubMed ID: 10894217)
1. Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.
Klein C; Pramstaller PP; Kis B; Page CC; Kann M; Leung J; Woodward H; Castellan CC; Scherer M; Vieregge P; Breakefield XO; Kramer PL; Ozelius LJ
Ann Neurol; 2000 Jul; 48(1):65-71. PubMed ID: 10894217
[TBL] [Abstract][Full Text] [Related]
2. Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.
Valente EM; Bentivoglio AR; Dixon PH; Ferraris A; Ialongo T; Frontali M; Albanese A; Wood NW
Am J Hum Genet; 2001 Apr; 68(4):895-900. PubMed ID: 11254447
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 10072423
[TBL] [Abstract][Full Text] [Related]
4. 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; ;
N Engl J Med; 2000 May; 342(21):1560-7. PubMed ID: 10824074
[TBL] [Abstract][Full Text] [Related]
5. Clinical findings in a large family with a parkin ex3delta40 mutation.
Munhoz RP; Sa DS; Rogaeva E; Salehi-Rad S; Sato C; Medeiros H; Farrer M; Lang AE
Arch Neurol; 2004 May; 61(5):701-4. PubMed ID: 15148147
[TBL] [Abstract][Full Text] [Related]
6. Homozygous exon 4 deletion in parkin gene in a Korean family with autosomal recessive early onset parkinsonism.
Kim JS; Lee KS; Kim YI; Lee KH; Kim HT
Yonsei Med J; 2003 Apr; 44(2):336-9. PubMed ID: 12728478
[TBL] [Abstract][Full Text] [Related]
7. Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.
Wu RM; Bounds R; Lincoln S; Hulihan M; Lin CH; Hwu WL; Chen J; Gwinn-Hardy K; Farrer M
Arch Neurol; 2005 Jan; 62(1):82-7. PubMed ID: 15642853
[TBL] [Abstract][Full Text] [Related]
8. Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene.
Hilker R; Klein C; Ghaemi M; Kis B; Strotmann T; Ozelius LJ; Lenz O; Vieregge P; Herholz K; Heiss WD; Pramstaller PP
Ann Neurol; 2001 Mar; 49(3):367-76. PubMed ID: 11261512
[TBL] [Abstract][Full Text] [Related]
9. Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.
Gouider-Khouja N; Larnaout A; Amouri R; Sfar S; Belal S; Ben Hamida C; Ben Hamida M; Hattori N; Mizuno Y; Hentati F
Parkinsonism Relat Disord; 2003 Jun; 9(5):247-51. PubMed ID: 12781588
[TBL] [Abstract][Full Text] [Related]
10. Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa.
Ibáñez P; Lesage S; Lohmann E; Thobois S; De Michele G; Borg M; Agid Y; Dürr A; Brice A;
Brain; 2006 Mar; 129(Pt 3):686-94. PubMed ID: 16401616
[TBL] [Abstract][Full Text] [Related]
11. Detection of compound heterozygous deletions in the parkin gene of fibroblasts in patients with autosomal recessive hereditary parkinsonism (PARK2).
Nakaso K; Adachi Y; Yasui K; Sakuma K; Nakashima K
Neurosci Lett; 2006 May; 400(1-2):44-7. PubMed ID: 16517073
[TBL] [Abstract][Full Text] [Related]
12. 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; 8():47. PubMed ID: 19087301
[TBL] [Abstract][Full Text] [Related]
13. Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism.
Lesage S; Magali P; Lohmann E; Lacomblez L; Teive H; Janin S; Cousin PY; Dürr A; Brice A;
Hum Mutat; 2007 Jan; 28(1):27-32. PubMed ID: 17068781
[TBL] [Abstract][Full Text] [Related]
14. [Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].
Hattori N
Rinsho Shinkeigaku; 2004; 44(4-5):241-62. PubMed ID: 15287506
[TBL] [Abstract][Full Text] [Related]
15. Relative high frequency of the c.255delA parkin gene mutation in Spanish patients with autosomal recessive parkinsonism.
Muñoz E; Tolosa E; Pastor P; Martí MJ; Valldeoriola F; Campdelacreu J; Oliva R
J Neurol Neurosurg Psychiatry; 2002 Nov; 73(5):582-4. PubMed ID: 12397156
[TBL] [Abstract][Full Text] [Related]
16. Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7.
Bonifati V; Dekker MC; Vanacore N; Fabbrini G; Squitieri F; Marconi R; Antonini A; Brustenghi P; Dalla Libera A; De Mari M; Stocchi F; Montagna P; Gallai V; Rizzu P; van Swieten JC; Oostra B; van Duijn CM; Meco G; Heutink P;
Neurol Sci; 2002 Sep; 23 Suppl 2():S59-60. PubMed ID: 12548343
[TBL] [Abstract][Full Text] [Related]
17. Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.
Hattori N; Kitada T; Matsumine H; Asakawa S; Yamamura Y; Yoshino H; Kobayashi T; Yokochi M; Wang M; Yoritaka A; Kondo T; Kuzuhara S; Nakamura S; Shimizu N; Mizuno Y
Ann Neurol; 1998 Dec; 44(6):935-41. PubMed ID: 9851438
[TBL] [Abstract][Full Text] [Related]
18. Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism.
Bonifati V; Lücking CB; Fabrizio E; Periquet M; Meco G; Brice A
J Neurol Neurosurg Psychiatry; 2001 Oct; 71(4):531-4. PubMed ID: 11561042
[TBL] [Abstract][Full Text] [Related]
19. Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism.
Illarioshkin SN; Periquet M; Rawal N; Lücking CB; Zagorovskaya TB; Slominsky PA; Miloserdova OV; Markova ED; Limborska SA; Ivanova-Smolenskaya IA; Brice A
Mov Disord; 2003 Aug; 18(8):914-9. PubMed ID: 12889082
[TBL] [Abstract][Full Text] [Related]
20. The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Bonifati V; De Michele G; Lücking CB; Dürr A; Fabrizio E; Ambrosio G; Vanacore N; De Mari M; Marconi R; Capus L; Breteler MM; Gasser T; Oostra B; Wood N; Agid Y; Filla A; Meco G; Brice A;
Neurol Sci; 2001 Feb; 22(1):51-2. PubMed ID: 11487197
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
