BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 7424977)

  • 1. Linkage studies in spinocerebellar ataxia (SCA).
    Morton NE; Lalouel JM; Jackson JF; Currier RD; Yee S
    Am J Med Genet; 1980; 6(3):251-7. PubMed ID: 7424977
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Linkage study of hereditary olivopontocerebellar atrophy: genetic evidence for locus heterogeneity in Japanese cases].
    Sasaki H; Wakisaka A; Tashiro K; Hamada T; Shima K
    Rinsho Shinkeigaku; 1992 Jan; 32(1):17-22. PubMed ID: 1628432
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Linkage study of Machado-Joseph disease: genetic evidence for the locus different from SCA1].
    Sasaki H; Wakisaka A; Tashiro K; Hamada T; Katoh T
    Rinsho Shinkeigaku; 1992 Jan; 32(1):13-6. PubMed ID: 1628431
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic heterogeneity of dominantly inherited olivopontocerebellar atrophy (OPCA) in the Japanese: linkage study of two pedigrees and evidence for the disease locus on chromosome 12q (SCA2).
    Ihara T; Sasaki H; Wakisaka A; Takada A; Yoshiki T; Matsuura T; Hamada T; Suzuki Y; Tashiro K
    Jpn J Hum Genet; 1994 Sep; 39(3):305-13. PubMed ID: 7841441
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing.
    Jackson JF; Currier RD; Terasaki PI; Morton NE
    N Engl J Med; 1977 May; 296(20):1138-41. PubMed ID: 857157
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A clinical study of a family affected with HLA-linked hereditary spinocerebellar ataxia].
    Sasaki H; Hamada T; Wakisaka A; Tashiro K
    No To Shinkei; 1990 Nov; 42(11):1103-11. PubMed ID: 2076357
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.
    Verbeek DS; Schelhaas JH; Ippel EF; Beemer FA; Pearson PL; Sinke RJ
    Hum Genet; 2002 Oct; 111(4-5):388-93. PubMed ID: 12384780
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2).
    Dürr A; Brice A; Lepage-Lezin A; Cancel G; Smadja D; Vernant JC; Agid Y
    Clin Neurosci; 1995; 3(1):12-6. PubMed ID: 7614088
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I.
    Benomar A; Le Guern E; Dürr A; Ouhabi H; Stevanin G; Yahyaoui M; Chkili T; Agid Y; Brice A
    Ann Neurol; 1994 Apr; 35(4):439-44. PubMed ID: 8154871
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic linkage with HLA in spinocerebellar ataxia.
    Noreen HJ; Nino HE; Dubey DP; Resch JA; Namboodiri K; Elston RC; Yunis EJ
    Transplant Proc; 1979 Dec; 11(4):1729-31. PubMed ID: 531925
    [No Abstract]   [Full Text] [Related]  

  • 11. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
    Brkanac Z; Fernandez M; Matsushita M; Lipe H; Wolff J; Bird TD; Raskind WH
    Am J Med Genet; 2002 May; 114(4):450-7. PubMed ID: 11992570
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.
    Gispert S; Twells R; Orozco G; Brice A; Weber J; Heredero L; Scheufler K; Riley B; Allotey R; Nothers C
    Nat Genet; 1993 Jul; 4(3):295-9. PubMed ID: 8358438
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Spinocerebellar ataxia 1--clinical study of 17 patients in a large pedigree].
    Sasaki H; Wakisaka A; Koyama T; Hamada T; Shima K; Tashiro K; Hashimoto K; Miyagishi T
    No To Shinkei; 1993 Jun; 45(6):502-8. PubMed ID: 8363844
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Clinical study of two families with late-onset autosomal dominant spinal-cerebellar ataxia linked with HLA. Preliminary results].
    Giunti P; Spadaro M; Frontali M; Bianco F; Morocutti C
    Riv Neurol; 1990; 60(5):176-9. PubMed ID: 2100035
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic approaches to the nosology of nervous system defects.
    Becker PE
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):10-22. PubMed ID: 5173354
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Clinical study of gene locus heterogeneity in hereditary olivopontocerebellar atrophy (OPCA)--report of 2 pedigrees affected with non SCA1 type OPCA].
    Sasaki H; Wakisaka A; Tashiro K; Hamada T; Shima K
    Rinsho Shinkeigaku; 1991 Nov; 31(11):1170-6. PubMed ID: 1813183
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
    Stevanin G; Bouslam N; Thobois S; Azzedine H; Ravaux L; Boland A; Schalling M; Broussolle E; Dürr A; Brice A
    Ann Neurol; 2004 Jan; 55(1):97-104. PubMed ID: 14705117
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6.
    Haines JL; Trofatter JA
    Genet Epidemiol; 1986; 3(6):399-405. PubMed ID: 3468044
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetics of the SCA6 gene in a large family segregating an autosomal dominant "pure" cerebellar ataxia.
    García-Planells J; Cuesta A; Vilchez JJ; Martínez F; Prieto F; Palau F
    J Med Genet; 1999 Feb; 36(2):148-51. PubMed ID: 10051016
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.
    Thiffault I; Rioux MF; Tetreault M; Jarry J; Loiselle L; Poirier J; Gros-Louis F; Mathieu J; Vanasse M; Rouleau GA; Bouchard JP; Lesage J; Brais B
    Brain; 2006 Sep; 129(Pt 9):2332-40. PubMed ID: 16672289
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.