148 related articles for article (PubMed ID: 7847859)
21. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
Oda M; Maruyama H; Komure O; Morino H; Terasawa H; Izumi Y; Imamura T; Yasuda M; Ichikawa K; Ogawa M; Matsumoto M; Kawakami H
Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767
[TBL] [Abstract][Full Text] [Related]
22. The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias.
Giunti P; Sweeney MG; Spadaro M; Jodice C; Novelletto A; Malaspina P; Frontali M; Harding AE
Brain; 1994 Aug; 117 ( Pt 4)():645-9. PubMed ID: 7922453
[TBL] [Abstract][Full Text] [Related]
23. [Spinocerebellar ataxia: advances in genetic research and its clinical implication].
Sasaki H
Hokkaido Igaku Zasshi; 1997 Jan; 72(1):13-20. PubMed ID: 9086358
[TBL] [Abstract][Full Text] [Related]
24. Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
Stevanin G; Hahn V; Lohmann E; Bouslam N; Gouttard M; Soumphonphakdy C; Welter ML; Ollagnon-Roman E; Lemainque A; Ruberg M; Brice A; Durr A
Arch Neurol; 2004 Aug; 61(8):1242-8. PubMed ID: 15313841
[TBL] [Abstract][Full Text] [Related]
25. A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families.
Warner TT; Williams LD; Walker RW; Flinter F; Robb SA; Bundey SE; Honavar M; Harding AE
Ann Neurol; 1995 Apr; 37(4):452-9. PubMed ID: 7717681
[TBL] [Abstract][Full Text] [Related]
26. Uncloned expanded CAG/CTG repeat sequences in autosomal dominant cerebellar ataxia (ADCA) detected by the repeat expansion detection (RED) method.
Pujana MA; Volpini V; Gratacós M; Corral J; Banchs I; Sánchez A; Genís D; Cervera C; Estivill X
J Med Genet; 1998 Feb; 35(2):99-102. PubMed ID: 9507387
[TBL] [Abstract][Full Text] [Related]
27. [Clinical and genetic characteristics of SCA1].
Abe K
Nihon Rinsho; 1999 Apr; 57(4):796-800. PubMed ID: 10222768
[TBL] [Abstract][Full Text] [Related]
28. Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia.
Ranum LP; Lundgren JK; Schut LJ; Ahrens MJ; Perlman S; Aita J; Bird TD; Gomez C; Orr HT
Am J Hum Genet; 1995 Sep; 57(3):603-8. PubMed ID: 7668288
[TBL] [Abstract][Full Text] [Related]
29. Dominantly inherited ataxias.
Subramony SH; Vig PJ; McDaniel DO
Semin Neurol; 1999; 19(4):419-25. PubMed ID: 10716664
[TBL] [Abstract][Full Text] [Related]
30. Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.
Ranum LP; Chung MY; Banfi S; Bryer A; Schut LJ; Ramesar R; Duvick LA; McCall A; Subramony SH; Goldfarb L
Am J Hum Genet; 1994 Aug; 55(2):244-52. PubMed ID: 8037204
[TBL] [Abstract][Full Text] [Related]
31. Analysis of CAG trinucleotide expansion associated with Machado-Joseph disease.
Watanabe M; Abe K; Aoki M; Kameya T; Kaneko J; Shoji M; Ikeda M; Shizuka M; Ikeda Y; Iizuka T; Hirai S; Itoyama Y
J Neurol Sci; 1996 Mar; 136(1-2):101-7. PubMed ID: 8815156
[TBL] [Abstract][Full Text] [Related]
32. Machado-Joseph disease.
Sudarsky L; Coutinho P
Clin Neurosci; 1995; 3(1):17-22. PubMed ID: 7614089
[TBL] [Abstract][Full Text] [Related]
33. Genetic anticipation. Expanding tandem repeats.
Carpenter NJ
Neurol Clin; 1994 Nov; 12(4):683-97. PubMed ID: 7845337
[TBL] [Abstract][Full Text] [Related]
34. [Clinical study of two families with late-onset autosomal dominant spinal-cerebellar ataxia linked with HLA. Preliminary results].
Giunti P; Spadaro M; Frontali M; Bianco F; Morocutti C
Riv Neurol; 1990; 60(5):176-9. PubMed ID: 2100035
[TBL] [Abstract][Full Text] [Related]
35. SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene.
Koht J; Stevanin G; Durr A; Mundwiller E; Brice A; Tallaksen CM
Acta Neurol Scand; 2012 Feb; 125(2):116-22. PubMed ID: 21434874
[TBL] [Abstract][Full Text] [Related]
36. [Genetic diagnosis, classification and clinical hereditary ataxia disease entities].
Schöls L; Riess O; Amoiridis G; Riess A; Przuntek H; Epplen JT
Fortschr Neurol Psychiatr; 1997 Feb; 65(2):79-89. PubMed ID: 9157050
[TBL] [Abstract][Full Text] [Related]
37. Autosomal dominant cerebellar ataxias in the Kinki area of Japan.
Matsumura R; Takayanagi T; Murata K; Futamura N; Fujimoto Y
Jpn J Hum Genet; 1996 Dec; 41(4):399-406. PubMed ID: 9088110
[TBL] [Abstract][Full Text] [Related]
38. Trinucleotide repeat expansion of spinocerebellar ataxia (SCA1) found in a Chinese family.
Cai T; Yu P; Chen X; Lopa M
Chin Med J (Engl); 1998 Feb; 111(2):160-2. PubMed ID: 10374379
[TBL] [Abstract][Full Text] [Related]
39. Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan.
Kameya T; Abe K; Aoki M; Sahara M; Tobita M; Konno H; Itoyama Y
Neurology; 1995 Aug; 45(8):1587-94. PubMed ID: 7543989
[TBL] [Abstract][Full Text] [Related]
40. Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.
Ishikawa K; Tanaka H; Saito M; Ohkoshi N; Fujita T; Yoshizawa K; Ikeuchi T; Watanabe M; Hayashi A; Takiyama Y; Nishizawa M; Nakano I; Matsubayashi K; Miwa M; Shoji S; Kanazawa I; Tsuji S; Mizusawa H
Am J Hum Genet; 1997 Aug; 61(2):336-46. PubMed ID: 9311738
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
