These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 7902323)

  • 21. Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population.
    Auburger G; Diaz GO; Capote RF; Sanchez SG; Perez MP; del Cueto ME; Meneses MG; Farrall M; Williamson R; Chamberlain S
    Am J Hum Genet; 1990 Jun; 46(6):1163-77. PubMed ID: 1971152
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family.
    Martin JJ; Van Regemorter N; Krols L; Brucher JM; de Barsy T; Szliwowski H; Evrard P; Ceuterick C; Tassignon MJ; Smet-Dieleman H
    Acta Neuropathol; 1994; 88(4):277-86. PubMed ID: 7839819
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.
    Cancel G; Abbas N; Stevanin G; Dürr A; Chneiweiss H; Néri C; Duyckaerts C; Penet C; Cann HM; Agid Y
    Am J Hum Genet; 1995 Oct; 57(4):809-16. PubMed ID: 7573040
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.
    Vale J; Bugalho P; Silveira I; Sequeiros J; Guimarães J; Coutinho P
    Eur J Neurol; 2010 Jan; 17(1):124-8. PubMed ID: 19659750
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locus.
    Lopes-Cendes I; Andermann E; Rouleau GA
    Genomics; 1994 May; 21(1):270-4. PubMed ID: 8088802
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [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]  

  • 30. Search for the chromosomal location of autosomal dominant cerebellar ataxia from Holguin, Cuba: exclusion from candidate regions on chromosome 4 and 11q.
    Gispert S; Nothers C; Orozco G; Auburger G
    Hum Hered; 1993; 43(1):12-20. PubMed ID: 8514320
    [TBL] [Abstract][Full Text] [Related]  

  • 31. DNA marker studies show that Machado Joseph disease is not an allele of the Huntington disease locus.
    Forse RA; MacLeod P; Holden JJ; White BN
    J Neurogenet; 1989 May; 5(2):155-8. PubMed ID: 2525613
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. Machado-Joseph disease.
    Sudarsky L; Coutinho P
    Clin Neurosci; 1995; 3(1):17-22. PubMed ID: 7614089
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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]  

  • 37. Machado-Joseph disease: clinical, molecular, and metabolic characterization in Chinese kindreds.
    Soong B; Cheng C; Liu R; Shan D
    Ann Neurol; 1997 Apr; 41(4):446-52. PubMed ID: 9124801
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease.
    Lopes-Cendes I; Maciel P; Kish S; Gaspar C; Robitaille Y; Clark HB; Koeppen AH; Nance M; Schut L; Silveira I; Coutinho P; Sequeiros J; Rouleau GA
    Ann Neurol; 1996 Aug; 40(2):199-206. PubMed ID: 8773601
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Origins and Spread of Machado-Joseph Disease Ancestral Mutations Events.
    Martins S; Sequeiros J
    Adv Exp Med Biol; 2018; 1049():243-254. PubMed ID: 29427107
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias.
    Stevanin G; Trottier Y; Cancel G; Dürr A; David G; Didierjean O; Bürk K; Imbert G; Saudou F; Abada-Bendib M; Gourfinkel-An I; Benomar A; Abbas N; Klockgether T; Grid D; Agid Y; Mandel JL; Brice A
    Hum Mol Genet; 1996 Dec; 5(12):1887-92. PubMed ID: 8968739
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.