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 *

797 related articles for article (PubMed ID: 9772474)

  • 21. Intrafamilial variability of Parkinson phenotype in SCAs: novel cases due to SCA2 and SCA3 expansions.
    Socal MP; Emmel VE; Rieder CR; Hilbig A; Saraiva-Pereira ML; Jardim LB
    Parkinsonism Relat Disord; 2009 Jun; 15(5):374-8. PubMed ID: 18990604
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. [Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes].
    Chen P; Ma M; Shang H; Su D; Zhang S; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):626-33. PubMed ID: 19953483
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxia.
    Lorenzetti D; Bohlega S; Zoghbi HY
    Neurology; 1997 Oct; 49(4):1009-13. PubMed ID: 9339681
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations.
    Takano H; Cancel G; Ikeuchi T; Lorenzetti D; Mawad R; Stevanin G; Didierjean O; Dürr A; Oyake M; Shimohata T; Sasaki R; Koide R; Igarashi S; Hayashi S; Takiyama Y; Nishizawa M; Tanaka H; Zoghbi H; Brice A; Tsuji S
    Am J Hum Genet; 1998 Oct; 63(4):1060-6. PubMed ID: 9758625
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients.
    Sułek-Piatkowska A; Zdzienicka E; Raczyńska-Rakowicz M; Krysa W; Rajkiewicz M; Szirkowiec W; Zaremba J
    Neurol Neurochir Pol; 2010; 44(3):238-45. PubMed ID: 20625959
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism.
    Lin CH; Hwu WL; Chiang SC; Tai CH; Wu RM
    Am J Med Genet B Neuropsychiatr Genet; 2007 Jun; 144B(4):434-8. PubMed ID: 17440947
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
    Yin XZ; Zhang BR; Wu DW; Tian J; Zhang H
    Yi Chuan; 2007 Jun; 29(6):688-92. PubMed ID: 17650485
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.
    Jiang H; Tang B; Xia K; Zhou Y; Xu B; Zhao G; Li H; Shen L; Pan Q; Cai F
    J Neurol Sci; 2005 Sep; 236(1-2):25-9. PubMed ID: 15979648
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Molecular and prenatal diagnosis of a pedigree with spinocerebellar ataxia].
    Cao DH; Ren MH; Liu XL; Jin CL; Meng ZY; Qiu GB
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Jun; 27(3):320-3. PubMed ID: 20533274
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic.
    Wang YG; Du J; Wang JL; Chen J; Chen C; Luo YY; Xiao ZQ; Jiang H; Yan XX; Xia K; Pan Q; Tang BS; Shen L
    J Neurol Sci; 2009 Oct; 285(1-2):121-4. PubMed ID: 19608203
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia.
    Ranum LP; Lundgren JK; Schut LJ; Ahrens MJ; Perlman S; Aita J; Bird TD; Gomez C; Orr HT
    Am J Hum Genet; 1995 Sep; 57(3):603-8. PubMed ID: 7668288
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [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]  

  • 35. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
    Dürr A; Stevanin G; Cancel G; Duyckaerts C; Abbas N; Didierjean O; Chneiweiss H; Benomar A; Lyon-Caen O; Julien J; Serdaru M; Penet C; Agid Y; Brice A
    Ann Neurol; 1996 Apr; 39(4):490-9. PubMed ID: 8619527
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Gene diagnosis and CAG repeat analysis of spinocerebellar ataxia cases of Guangxi region].
    Tan JQ; Wang P; Hu QP; Li SF; Shu W; Ma J; Fang L; Hua R; Ding Y; Yuan ZG
    Yi Chuan; 2009 Jun; 31(6):605-10. PubMed ID: 19586860
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.
    de Castilhos RM; Furtado GV; Gheno TC; Schaeffer P; Russo A; Barsottini O; Pedroso JL; Salarini DZ; Vargas FR; de Lima MA; Godeiro C; Santana-da-Silva LC; Toralles MB; Santos S; van der Linden H; Wanderley HY; de Medeiros PF; Pereira ET; Ribeiro E; Saraiva-Pereira ML; Jardim LB;
    Cerebellum; 2014 Feb; 13(1):17-28. PubMed ID: 23943520
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 families.
    Zhou YX; Qiao WH; Gu WH; Xie H; Tang BS; Zhou LS; Yang BX; Takiyama Y; Tsuji S; He HY; Deng CX; Goldfarb LG; Wang GX
    Arch Neurol; 2001 May; 58(5):789-94. PubMed ID: 11346374
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.
    Leggo J; Dalton A; Morrison PJ; Dodge A; Connarty M; Kotze MJ; Rubinsztein DC
    J Med Genet; 1997 Dec; 34(12):982-5. PubMed ID: 9429138
    [TBL] [Abstract][Full Text] [Related]  

  • 40. SCA2 trinucleotide expansion in German SCA patients.
    Riess O; Laccone FA; Gispert S; Schöls L; Zühlke C; Vieira-Saecker AM; Herlt S; Wessel K; Epplen JT; Weber BH; Kreuz F; Chahrokh-Zadeh S; Meindl A; Lunkes A; Aguiar J; Macek M; Krebsová A; Macek M; Bürk K; Tinschert S; Schreyer I; Pulst SM; Auburger G
    Neurogenetics; 1997 May; 1(1):59-64. PubMed ID: 10735276
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 40.