BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 8655151)

  • 1. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families.
    Lezin A; Cancel G; Stevanin G; Smadja D; Vernant JC; Dürr A; Martial J; Buisson GG; Bellance R; Chneiweiss H; Agid Y; Brice A
    Hum Genet; 1996 May; 97(5):671-6. PubMed ID: 8655151
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus.
    Belal S; Cancel G; Stevanin G; Hentati F; Khati C; Ben Hamida C; Auburger G; Agid Y; Ben Hamida M; Brice A
    Neurology; 1994 Aug; 44(8):1423-6. PubMed ID: 8058142
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SCA2 is not a major locus for ADCA type I in French families.
    Cancel G; Stevanin G; Dürr A; Chneiweiss H; Penet C; Pothin Y; Agid Y; Brice A
    Am J Med Genet; 1995 Oct; 60(5):382-5. PubMed ID: 8546150
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12.
    Nechiporuk A; Lopes-Cendes I; Nechiporuk T; Starkman S; Andermann E; Rouleau GA; Weissenbach JS; Kort E; Pulst SM
    Neurology; 1996 Jun; 46(6):1731-5. PubMed ID: 8649579
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1.
    Hernández A; Magariño C; Gispert S; Santos N; Lunkes A; Orozco G; Heredero L; Beckmann J; Auburger G
    Genomics; 1995 Jan; 25(2):433-5. PubMed ID: 7789976
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
    Chung MY; Lu YC; Cheng NC; Soong BW
    Brain; 2003 Jun; 126(Pt 6):1293-9. PubMed ID: 12764052
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.
    Zu L; Figueroa KP; Grewal R; Pulst SM
    Am J Hum Genet; 1999 Feb; 64(2):594-9. PubMed ID: 9973298
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus.
    Twells R; Yenchitsomanus PT; Sirinavin C; Allotey R; Poungvarin N; Viriyavejakul A; Cemal C; Weber J; Farrall M; Rodprasert P
    Hum Mol Genet; 1994 Jan; 3(1):177-80. PubMed ID: 8162021
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus.
    Stevanin G; Le Guern E; Ravisé N; Chneiweiss H; Dürr A; Cancel G; Vignal A; Boch AL; Ruberg M; Penet C
    Am J Hum Genet; 1994 Jan; 54(1):11-20. PubMed ID: 8279460
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families.
    Dürr A; Smadja D; Cancel G; Lezin A; Stevanin G; Mikol J; Bellance R; Buisson GG; Chneiweiss H; Dellanave J
    Brain; 1995 Dec; 118 ( Pt 6)():1573-81. PubMed ID: 8595486
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family.
    Filla A; De Michele G; Banfi S; Santoro L; Perretti A; Cavalcanti F; Pianese L; Castaldo I; Barbieri F; Campanella G
    Neurology; 1995 Apr; 45(4):793-6. PubMed ID: 7723972
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.
    Ranum LP; Schut LJ; Lundgren JK; Orr HT; Livingston DM
    Nat Genet; 1994 Nov; 8(3):280-4. PubMed ID: 7874171
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2.
    Stevanin G; Cancel G; Dürr A; Chneiweiss H; Dubourg O; Weissenbach J; Cann HM; Agid Y; Brice A
    Am J Hum Genet; 1995 Jan; 56(1):193-201. PubMed ID: 7825578
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.