197 related articles for article (PubMed ID: 9588855)
1. Analysis of spinocerebellar ataxia type 2 in Gunma Prefecture in Japan: CAG trinucleotide expansion and clinical characteristics.
Mizushima K; Watanabe M; Abe K; Aoki M; Itoyama Y; Shizuka M; Okamoto K; Shoji M
J Neurol Sci; 1998 Apr; 156(2):180-5. PubMed ID: 9588855
[TBL] [Abstract][Full Text] [Related]
2. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
[TBL] [Abstract][Full Text] [Related]
3. [Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese].
Ikeuchi T
Nihon Rinsho; 1999 Apr; 57(4):891-5. PubMed ID: 10222785
[TBL] [Abstract][Full Text] [Related]
4. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.
Matilla T; McCall A; Subramony SH; Zoghbi HY
Ann Neurol; 1995 Jul; 38(1):68-72. PubMed ID: 7611728
[TBL] [Abstract][Full Text] [Related]
5. Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.
Schöls L; Gispert S; Vorgerd M; Menezes Vieira-Saecker AM; Blanke P; Auburger G; Amoiridis G; Meves S; Epplen JT; Przuntek H; Pulst SM; Riess O
Arch Neurol; 1997 Sep; 54(9):1073-80. PubMed ID: 9311350
[TBL] [Abstract][Full Text] [Related]
6. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.
Hashida H; Goto J; Kurisaki H; Mizusawa H; Kanazawa I
Ann Neurol; 1997 Apr; 41(4):505-11. PubMed ID: 9124808
[TBL] [Abstract][Full Text] [Related]
7. Identification of five spinocerebellar ataxia type 2 pedigrees in patients with autosomal dominant cerebellar ataxia in Taiwan.
Hsieh M; Li SY; Tsai CJ; Chen YY; Liu CS; Chang CY; Ro LS; Chen DF; Chen SS; Li C
Acta Neurol Scand; 1999 Sep; 100(3):189-94. PubMed ID: 10478584
[TBL] [Abstract][Full Text] [Related]
8. [The phenotype variation correlates with the size of CAG repeat in SCA2].
Sasaki H; Sanpei K
Nihon Rinsho; 1999 Apr; 57(4):818-21. PubMed ID: 10222772
[TBL] [Abstract][Full Text] [Related]
9. Phenotype variation correlates with CAG repeat length in SCA2--a study of 28 Japanese patients.
Sasaki H; Wakisaka A; Sanpei K; Takano H; Igarashi S; Ikeuchi T; Iwabuchi K; Fukazawa T; Hamada T; Yuasa T; Tsuji S; Tashiro K
J Neurol Sci; 1998 Aug; 159(2):202-8. PubMed ID: 9741408
[TBL] [Abstract][Full Text] [Related]
10. Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6.
Watanabe H; Tanaka F; Matsumoto M; Doyu M; Ando T; Mitsuma T; Sobue G
Clin Genet; 1998 Jan; 53(1):13-9. PubMed ID: 9550356
[TBL] [Abstract][Full Text] [Related]
11. [SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
Tang B; Wang D; Xia J
Zhonghua Yi Xue Za Zhi; 1997 Nov; 77(11):819-22. PubMed ID: 9772474
[TBL] [Abstract][Full Text] [Related]
12. The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxia.
Lorenzetti D; Bohlega S; Zoghbi HY
Neurology; 1997 Oct; 49(4):1009-13. PubMed ID: 9339681
[TBL] [Abstract][Full Text] [Related]
13. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
Pujana MA; Corral J; Gratacòs M; Combarros O; Berciano J; Genís D; Banchs I; Estivill X; Volpini V
Hum Genet; 1999 Jun; 104(6):516-22. PubMed ID: 10453742
[TBL] [Abstract][Full Text] [Related]
14. Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.
Ikeuchi T; Takano H; Koide R; Horikawa Y; Honma Y; Onishi Y; Igarashi S; Tanaka H; Nakao N; Sahashi K; Tsukagoshi H; Inoue K; Takahashi H; Tsuji S
Ann Neurol; 1997 Dec; 42(6):879-84. PubMed ID: 9403480
[TBL] [Abstract][Full Text] [Related]
15. Infantile onset spinocerebellar ataxia 2 (SCA2): a clinical report with review of previous cases.
Singh A; Faruq M; Mukerji M; Dwivedi MK; Pruthi S; Kapoor S
J Child Neurol; 2014 Jan; 29(1):139-44. PubMed ID: 24300164
[TBL] [Abstract][Full Text] [Related]
16. Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1-2 polymorphism and contribution to founder effect.
Mizushima K; Watanabe M; Kondo I; Okamoto K; Shizuka M; Abe K; Aoki M; Shoji M
J Med Genet; 1999 Feb; 36(2):112-4. PubMed ID: 10051008
[TBL] [Abstract][Full Text] [Related]
17. A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees. The significance of slow saccades in diagnosis.
Wadia N; Pang J; Desai J; Mankodi A; Desai M; Chamberlain S
Brain; 1998 Dec; 121 ( Pt 12)():2341-55. PubMed ID: 9874485
[TBL] [Abstract][Full Text] [Related]
18. [Molecular analyses of intergenerational instability of CAG repeat in SCA2 gene].
Igarashi S; Tsuji S
Nihon Rinsho; 1999 Apr; 57(4):811-7. PubMed ID: 10222771
[TBL] [Abstract][Full Text] [Related]
19. Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
Schöls L; Krüger R; Amoiridis G; Przuntek H; Epplen JT; Riess O
J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):67-73. PubMed ID: 9436730
[TBL] [Abstract][Full Text] [Related]
20. Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease.
Lopes-Cendes I; Maciel P; Kish S; Gaspar C; Robitaille Y; Clark HB; Koeppen AH; Nance M; Schut L; Silveira I; Coutinho P; Sequeiros J; Rouleau GA
Ann Neurol; 1996 Aug; 40(2):199-206. PubMed ID: 8773601
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
