105 related articles for article (PubMed ID: 7852812)
1. [Genetic diagnosis of hereditary spinocerebellar degeneration].
Ikeuchi T; Tsuji S
Nihon Naika Gakkai Zasshi; 1994 Nov; 83(11):2000-6. PubMed ID: 7852812
[No Abstract] [Full Text] [Related]
2. [SAC1 and SAC2: disease loci, gene defect, and clinical phenotypes].
Sasaki H; Tashiro K; Wakisaka A
No To Shinkei; 1995 Feb; 47(2):109-16. PubMed ID: 7669409
[No Abstract] [Full Text] [Related]
3. Anticipation in spinocerebellar ataxia type 2.
Pulst SM; Nechiporuk A; Starkman S
Nat Genet; 1993 Sep; 5(1):8-10. PubMed ID: 8220431
[No Abstract] [Full Text] [Related]
4. [Linkage analysis of hereditary spinocerebellar degeneration].
Wakisaka A; Sasaki H
Tanpakushitsu Kakusan Koso; 1993 Feb; 38(3):346-53. PubMed ID: 8098158
[No Abstract] [Full Text] [Related]
5. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
Orr HT; Chung MY; Banfi S; Kwiatkowski TJ; Servadio A; Beaudet AL; McCall AE; Duvick LA; Ranum LP; Zoghbi HY
Nat Genet; 1993 Jul; 4(3):221-6. PubMed ID: 8358429
[TBL] [Abstract][Full Text] [Related]
6. [Recent progress of research on hereditary spinocerebellar degeneration].
Wakisaka A; Sasaki H
Nihon Rinsho; 1993 Sep; 51(9):2467-73. PubMed ID: 8411730
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Hereditary ataxias in Akita prefecture].
Sugawara M; Toyoshima I; Kato K; Wada C; Imota T; Hirota K; Ishiguro H; Kagaya H; Hirata A; Ogasawara M; Masamune O
Rinsho Shinkeigaku; 1999 Jul; 39(7):763-6. PubMed ID: 10548917
[TBL] [Abstract][Full Text] [Related]
9. [Classification and diagnosis of degenerative ataxias].
Klockgether T; Bürk K; Auburger G; Dichgans J
Nervenarzt; 1995 Aug; 66(8):571-81. PubMed ID: 7566268
[TBL] [Abstract][Full Text] [Related]
10. Spinocerebellar ataxia type 1.
Zoghbi HY
Clin Neurosci; 1995; 3(1):5-11. PubMed ID: 7614095
[TBL] [Abstract][Full Text] [Related]
11. [Siblings with spinocerebellar ataxia type 1 (SCA 1)--diagnosis by detecting the expansion of CAG repeat on chromosome 6p].
Hanihara T; Takahashi T; Inoue K; Yamada Y; Iwabuchi K
Rinsho Shinkeigaku; 1994 May; 34(5):508-10. PubMed ID: 7924069
[TBL] [Abstract][Full Text] [Related]
12. Spinocerebellar degeneration.
Phanthumchinda K; Srikiatkachorn A
J Med Assoc Thai; 1991 Feb; 74(2):71-9. PubMed ID: 2056261
[TBL] [Abstract][Full Text] [Related]
13. Early onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia.
Kumar D; Blank CE
Indian Pediatr; 1989 Oct; 26(10):1014-9. PubMed ID: 2630444
[TBL] [Abstract][Full Text] [Related]
14. [Genes for human brain diseases--dentatorubral-pallidoluysian atrophy].
Naito H; Tsuji S
Tanpakushitsu Kakusan Koso; 1995 Apr; 40(6):829-33. PubMed ID: 7754068
[No Abstract] [Full Text] [Related]
15. Analysis of the CAG repeat and gene product in spinocerebellar ataxia type 1.
Zoghbi HY
Proc Assoc Am Physicians; 1995 Jul; 107(2):231-6. PubMed ID: 8624857
[No Abstract] [Full Text] [Related]
16. [Autosomal dominant spinocerebellar ataxia].
Legros B; Manto MU
Rev Med Brux; 1999 Dec; 20(6):495-503. PubMed ID: 10672773
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations.
Iwabuchi K; Tsuchiya K; Uchihara T; Yagishita S
Rev Neurol (Paris); 1999 Apr; 155(4):255-70. PubMed ID: 10367323
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Informed consent to the patient with hereditary ataxia].
Takayanagi T; Matumura R; Murata K
No To Shinkei; 1996 May; 48(5):437-42. PubMed ID: 8672302
[No Abstract] [Full Text] [Related]
20. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
Ben Hamida M; Attia-Romdhane N; Triki CH; Oueslati S; Hentati F
Rev Neurol (Paris); 1991; 147(12):798-808. PubMed ID: 1780608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]