286 related articles for article (PubMed ID: 9225982)
1. Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South african families.
Ramesar RS; Bardien S; Beighton P; Bryer A
Hum Genet; 1997 Jul; 100(1):131-7. PubMed ID: 9225982
[TBL] [Abstract][Full Text] [Related]
2. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.
Silveira I; Coutinho P; Maciel P; Gaspar C; Hayes S; Dias A; Guimarães J; Loureiro L; Sequeiros J; Rouleau GA
Am J Med Genet; 1998 Mar; 81(2):134-8. PubMed ID: 9613852
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. 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]
6. 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]
7. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
Tang B; Xia J; Wang D; Tang X; Shen L; Liu C; Dai H; Yan X; Pan Q; Xiao J; Zhang B; Ou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
[TBL] [Abstract][Full Text] [Related]
8. Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients.
Lopes-Cendes I; Teive HG; Calcagnotto ME; Da Costa JC; Cardoso F; Viana E; Maciel JA; Radvany J; Arruda WO; Trevisol-Bittencourt PC; Rosa Neto P; Silveira I; Steiner CE; Pinto Júnior W; Santos AS; Correa Neto Y; Werneck LC; Araújo AQ; Carakushansky G; Mello LR; Jardim LB; Rouleau GA
Arq Neuropsiquiatr; 1997 Sep; 55(3B):519-29. PubMed ID: 9629399
[TBL] [Abstract][Full Text] [Related]
9. Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients.
Silveira I; Lopes-Cendes I; Kish S; Maciel P; Gaspar C; Coutinho P; Botez MI; Teive H; Arruda W; Steiner CE; Pinto-Júnior W; Maciel JA; Jerin S; Sack G; Andermann E; Sudarsky L; Rosenberg R; MacLeod P; Chitayat D; Babul R; Sequeiros J; Rouleau GA
Neurology; 1996 Jan; 46(1):214-8. PubMed ID: 8559378
[TBL] [Abstract][Full Text] [Related]
10. Machado Joseph disease is not an allele of the spinocerebellar ataxia 2 locus.
Twist EC; Farrer LA; Macleod PM; Radvany J; Chamberlain S; Rosenberg RN; Rouleau GA
Hum Genet; 1994 Mar; 93(3):335-8. PubMed ID: 8125487
[TBL] [Abstract][Full Text] [Related]
11. The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1).
Carson WJ; Radvany J; Farrer LA; Vincent D; Rosenberg RN; MacLeod PM; Rouleau GA
Genomics; 1992 Jul; 13(3):852-5. PubMed ID: 1639414
[TBL] [Abstract][Full Text] [Related]
12. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
Geschwind DH; Perlman S; Figueroa CP; Treiman LJ; Pulst SM
Am J Hum Genet; 1997 Apr; 60(4):842-50. PubMed ID: 9106530
[TBL] [Abstract][Full Text] [Related]
13. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.
Tsai HF; Liu CS; Leu TM; Wen FC; Lin SJ; Liu CC; Yang DK; Li C; Hsieh M
Acta Neurol Scand; 2004 May; 109(5):355-60. PubMed ID: 15080863
[TBL] [Abstract][Full Text] [Related]
14. Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1.
Lopes-Cendes I; Steiner CE; Silveira I; Pinto Júnior W; Maciel JA; Rouleau GA
Arq Neuropsiquiatr; 1996 Sep; 54(3):412-8. PubMed ID: 9109985
[TBL] [Abstract][Full Text] [Related]
15. A survey of spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease-causing mutations.
Jardim LB; Silveira I; Pereira ML; Ferro A; Alonso I; do Céu Moreira M; Mendonça P; Ferreirinha F; Sequeiros J; Giugliani R
J Neurol; 2001 Oct; 248(10):870-6. PubMed ID: 11697524
[TBL] [Abstract][Full Text] [Related]
16. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
Dürr A; Stevanin G; Cancel G; Duyckaerts C; Abbas N; Didierjean O; Chneiweiss H; Benomar A; Lyon-Caen O; Julien J; Serdaru M; Penet C; Agid Y; Brice A
Ann Neurol; 1996 Apr; 39(4):490-9. PubMed ID: 8619527
[TBL] [Abstract][Full Text] [Related]
17. [Clinico-genetic study of type I spinocerebelllar ataxia].
Svetel M; Culjković B; Sternić N; Dragasević B; Stojković I; Romac S; Kostić VS
Srp Arh Celok Lek; 1999; 127(5-6):157-62. PubMed ID: 10500422
[TBL] [Abstract][Full Text] [Related]
18. Spinocerebellar ataxia, type 3 (SCA3) is genetically identical to Machado-Joseph disease (MJD).
Haberhausen G; Damian MS; Leweke F; Müller U
J Neurol Sci; 1995 Sep; 132(1):71-5. PubMed ID: 8523034
[TBL] [Abstract][Full Text] [Related]
19. Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of Walworth.
Giunti P; Sweeney MG; Harding AE
Brain; 1995 Oct; 118 ( Pt 5)():1077-85. PubMed ID: 7496771
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
