149 related articles for article (PubMed ID: 9710044)
1. Spinocerebellar ataxia type 2 in China: molecular analysis and genotype-phenotype correlation in nine families.
Zhou YX; Wang GX; Tang BS; Li WD; Wang DA; Lee HS; Sambuughin N; Zhou LS; Tsuji S; Yang BX; Goldfarb LG
Neurology; 1998 Aug; 51(2):595-8. PubMed ID: 9710044
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. 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]
4. 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]
5. The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.
Giunti P; Sabbadini G; Sweeney MG; Davis MB; Veneziano L; Mantuano E; Federico A; Plasmati R; Frontali M; Wood NW
Brain; 1998 Mar; 121 ( Pt 3)():459-67. PubMed ID: 9549522
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms.
Choudhry S; Mukerji M; Srivastava AK; Jain S; Brahmachari SK
Hum Mol Genet; 2001 Oct; 10(21):2437-46. PubMed ID: 11689490
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 families.
Zhou YX; Qiao WH; Gu WH; Xie H; Tang BS; Zhou LS; Yang BX; Takiyama Y; Tsuji S; He HY; Deng CX; Goldfarb LG; Wang GX
Arch Neurol; 2001 May; 58(5):789-94. PubMed ID: 11346374
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. [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]
14. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats.
Imbert G; Saudou F; Yvert G; Devys D; Trottier Y; Garnier JM; Weber C; Mandel JL; Cancel G; Abbas N; Dürr A; Didierjean O; Stevanin G; Agid Y; Brice A
Nat Genet; 1996 Nov; 14(3):285-91. PubMed ID: 8896557
[TBL] [Abstract][Full Text] [Related]
15. Spinocerebellar ataxia type 6. Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion.
Matsumura R; Futamura N; Fujimoto Y; Yanagimoto S; Horikawa H; Suzumura A; Takayanagi T
Neurology; 1997 Nov; 49(5):1238-43. PubMed ID: 9371900
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families.
Filla A; Mariotti C; Caruso G; Coppola G; Cocozza S; Castaldo I; Calabrese O; Salvatore E; De Michele G; Riggio MC; Pareyson D; Gellera C; Di Donato S
Eur Neurol; 2000; 44(1):31-6. PubMed ID: 10894992
[TBL] [Abstract][Full Text] [Related]
18. Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1.
Goldfarb LG; Vasconcelos O; Platonov FA; Lunkes A; Kipnis V; Kononova S; Chabrashvili T; Vladimirtsev VA; Alexeev VP; Gajdusek DC
Ann Neurol; 1996 Apr; 39(4):500-6. PubMed ID: 8619528
[TBL] [Abstract][Full Text] [Related]
19. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
Pulst SM; Nechiporuk A; Nechiporuk T; Gispert S; Chen XN; Lopes-Cendes I; Pearlman S; Starkman S; Orozco-Diaz G; Lunkes A; DeJong P; Rouleau GA; Auburger G; Korenberg JR; Figueroa C; Sahba S
Nat Genet; 1996 Nov; 14(3):269-76. PubMed ID: 8896555
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
