BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]
    of 6.