BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

305 related articles for article (PubMed ID: 10323319)

  • 21. [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]  

  • 22. A review of the inherited ataxias: recent advances in genetic, clinical and neuropathologic aspects.
    Furtado S; Das S; Suchowersky O
    Parkinsonism Relat Disord; 1998 Dec; 4(4):161-9. PubMed ID: 18591106
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Clinical and genetic analysis of spinocerebellar ataxia in Mali.
    Traoré M; Coulibaly T; Meilleur KG; La Pean A; Sangaré M; Landouré G; Mochel F; Karambé M; Guinto CO; Fischbeck KH
    Eur J Neurol; 2011 Oct; 18(10):1269-71. PubMed ID: 21418439
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese].
    Ikeuchi T
    Nihon Rinsho; 1999 Apr; 57(4):891-5. PubMed ID: 10222785
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
    Wolf NI; Koenig M
    Handb Clin Neurol; 2013; 113():1869-78. PubMed ID: 23622410
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. [Triplet repeat disorder, dentatorubral and pallidoluysian atrophy DRPLA)].
    Yamada M
    Nihon Rinsho; 1995 Apr; 53(4):1024-32. PubMed ID: 7752462
    [TBL] [Abstract][Full Text] [Related]  

  • 29. SCA-LSVD: a repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.
    Faruq M; Scaria V; Singh I; Tyagi S; Srivastava AK; Mukerji M
    Hum Mutat; 2009 Jul; 30(7):1037-42. PubMed ID: 19370769
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch families.
    Sinke RJ; Ippel EF; Diepstraten CM; Beemer FA; Wokke JH; van Hilten BJ; Knoers NV; van Amstel HK; Kremer HP
    Arch Neurol; 2001 Nov; 58(11):1839-44. PubMed ID: 11708993
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Growing genes cause neurological diseases].
    Johansson J; Holmgren G; Forsgren L; Holmberg M
    Lakartidningen; 1999 Feb; 96(8):897-900. PubMed ID: 10089735
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Asymptomatic CTG expansion at the SCA8 locus is associated with cerebellar atrophy on MRI.
    Ikeda Y; Shizuka-Ikeda M; Watanabe M; Schmitt M; Okamoto K; Shoji M
    J Neurol Sci; 2000 Dec; 182(1):76-9. PubMed ID: 11102643
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations.
    Geschwind DH; Perlman S; Figueroa KP; Karrim J; Baloh RW; Pulst SM
    Neurology; 1997 Nov; 49(5):1247-51. PubMed ID: 9371902
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Molecular basis of heterogeneities of clinical presentation of dentatorubral pallidoluysian atrophy (DRPLA)].
    Tsuji S
    Rinsho Shinkeigaku; 1994 Dec; 34(12):1227-9. PubMed ID: 7774119
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia.
    Topisirovic I; Dragasevic N; Savic D; Ristic A; Keckarevic M; Keckarevic D; Culjkovic B; Petrovic I; Romac S; Kostic VS
    Clin Genet; 2002 Oct; 62(4):321-4. PubMed ID: 12372061
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Focal dystonia as a presenting sign of spinocerebellar ataxia 17.
    Hagenah JM; Zühlke C; Hellenbroich Y; Heide W; Klein C
    Mov Disord; 2004 Feb; 19(2):217-20. PubMed ID: 14978680
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The CAG repeats number of spinocerebellar ataxia type 1 gene in normal Taiwanese and in patients with dominant inherited ataxia.
    Hsieh ML; Yang CY; Tsai HF; Chen YY; Li C; Li SY
    Proc Natl Sci Counc Repub China B; 1997 Jul; 21(3):91-5. PubMed ID: 9309871
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Infantile onset spinocerebellar ataxia 2 (SCA2): a clinical report with review of previous cases.
    Singh A; Faruq M; Mukerji M; Dwivedi MK; Pruthi S; Kapoor S
    J Child Neurol; 2014 Jan; 29(1):139-44. PubMed ID: 24300164
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Dentatorubral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLA.
    Ikeuchi T; Koide R; Onodera O; Tanaka H; Oyake M; Takano H; Tsuji S
    Clin Neurosci; 1995; 3(1):23-7. PubMed ID: 7614090
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.