126 related articles for article (PubMed ID: 15641013)
41. Clinical and genetic studies on familial parkinsonism: the first report on a parkin gene mutation in a Taiwanese family.
Lu CS; Wu JC; Tsai CH; Chen RS; Chou YH; Hattori N; Yoshino H; Mizuno Y
Mov Disord; 2001 Jan; 16(1):164-6. PubMed ID: 11215581
[No Abstract] [Full Text] [Related]
42. A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion.
Dogu O; Johnson J; Hernandez D; Hanson M; Hardy J; Apaydin H; Özekmekçi S; Sevim S; Gwinn-Hardy K; Singleton A
Mov Disord; 2004 Jul; 19(7):812-816. PubMed ID: 15254940
[TBL] [Abstract][Full Text] [Related]
43. Exon dosage variations in Brazilian patients with Parkinson's disease: analysis of SNCA, PARKIN, PINK1 and DJ-1 genes.
Moura KC; Junior MC; de Rosso AL; Nicaretta DH; Pereira JS; José Silva D; Santos-Rebouças CB; Pimentel MM
Dis Markers; 2012; 32(3):173-8. PubMed ID: 22377733
[TBL] [Abstract][Full Text] [Related]
44. Expanding phenotype and clinical heterogeneity in patients with identical mutation of the parkin gene.
Kunishige M; Mitsui T; Kuroda Y; Yoshida S; Kosaka M; Matsumoto T
Eur Neurol; 2004; 51(3):183-5. PubMed ID: 15073448
[No Abstract] [Full Text] [Related]
45. Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease.
Clarimon J; Johnson J; Dogu O; Horta W; Khan N; Lees AJ; Hardy J; Singleton A
Am J Med Genet B Neuropsychiatr Genet; 2005 Feb; 133B(1):120-3. PubMed ID: 15635662
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism.
Li Y; Tomiyama H; Sato K; Hatano Y; Yoshino H; Atsumi M; Kitaguchi M; Sasaki S; Kawaguchi S; Miyajima H; Toda T; Mizuno Y; Hattori N
Neurology; 2005 Jun; 64(11):1955-7. PubMed ID: 15955953
[TBL] [Abstract][Full Text] [Related]
48. Marked diurnal fluctuation and rest benefit in a patient with parkin mutation.
Chung SJ; Park HK; Ki CS; Kim MJ; Lee MC
Mov Disord; 2008 Mar; 23(4):624-6. PubMed ID: 18228570
[No Abstract] [Full Text] [Related]
49. [Exon rearrangement analysis of parkin gene in patients with isolated early-onset parkinsonism using semi-quantitative PCR].
Guo JF; Tang BS; Li J; Zhang YH; Zhang XW; Chen T; Xia K; Yan XX; Cao L; Cai F; Pan Q; Shen L; Jiang H
Zhonghua Yi Xue Za Zhi; 2006 Jun; 86(21):1447-9. PubMed ID: 16842693
[TBL] [Abstract][Full Text] [Related]
50. [Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism].
Guo JF; Tang BS; Zhang YH; Liu HJ; Yan XX; Chen T; Shen L; Jiang H; Xia K; Cai F; Pan Q
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Feb; 23(1):70-3. PubMed ID: 16456791
[TBL] [Abstract][Full Text] [Related]
51. Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin gene.
Nisipeanu P; Inzelberg R; Blumen SC; Carasso RL; Hattori N; Matsumine H; Mizuno Y
Neurology; 1999 Oct; 53(7):1602-4. PubMed ID: 10534280
[TBL] [Abstract][Full Text] [Related]
52. 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]
53. 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]
54. Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome.
Wickremaratchi MM; Majounie E; Morris HR; Williams NM; Lewis H; Gill SS; Khan S; Heywood P; Hardy J; Wiles CM; Singleton AB; Quinn NP
Mov Disord; 2009 Jan; 24(1):138-40. PubMed ID: 18942080
[No Abstract] [Full Text] [Related]
55. Exercise-induced dystonia as a preceding symptom of familial Parkinson's disease.
Bruno MK; Ravina B; Garraux G; Hallett M; Ptacek L; Singleton A; Johnson J; Singleton A; Hanson M; Considine E; Gwinn-Hardy K
Mov Disord; 2004 Feb; 19(2):228-30. PubMed ID: 14978684
[TBL] [Abstract][Full Text] [Related]
56. Distribution, type, and origin of Parkin mutations: review and case studies.
Hedrich K; Eskelson C; Wilmot B; Marder K; Harris J; Garrels J; Meija-Santana H; Vieregge P; Jacobs H; Bressman SB; Lang AE; Kann M; Abbruzzese G; Martinelli P; Schwinger E; Ozelius LJ; Pramstaller PP; Klein C; Kramer P
Mov Disord; 2004 Oct; 19(10):1146-57. PubMed ID: 15390068
[TBL] [Abstract][Full Text] [Related]
57. Decades of delayed diagnosis in 4 levodopa-responsive young-onset monogenetic parkinsonism patients.
Ling H; Braschinsky M; Taba P; Lüüs SM; Doherty K; Hotter A; Poewe W; Lees AJ
Mov Disord; 2011 Jun; 26(7):1337-40. PubMed ID: 21449012
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. 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]
60. T313M PINK1 mutation in an extended highly consanguineous Saudi family with early-onset Parkinson disease.
Chishti MA; Bohlega S; Ahmed M; Loualich A; Carroll P; Sato C; St George-Hyslop P; Westaway D; Rogaeva E
Arch Neurol; 2006 Oct; 63(10):1483-5. PubMed ID: 17030667
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
