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Journal Abstract Search

294 related items for PubMed ID: 9086358

  • 1. [Spinocerebellar ataxia: advances in genetic research and its clinical implication].
    Sasaki H.
    Hokkaido Igaku Zasshi; 1997 Jan; 72(1):13-20. PubMed ID: 9086358
    [Abstract] [Full Text] [Related]

  • 2. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
    Tang B, Xia J, Wang D, Tang X, Shen L, Liu C, Dai H, Yan X, Pan Q, Xiao J, Zhang B, Ou Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.
    Silveira I, Coutinho P, Maciel P, Gaspar C, Hayes S, Dias A, Guimarães J, Loureiro L, Sequeiros J, Rouleau GA.
    Am J Med Genet; 1998 Mar 28; 81(2):134-8. PubMed ID: 9613852
    [Abstract] [Full Text] [Related]

  • 5. [Autosomal dominant spinocerebellar ataxia].
    Legros B, Manto MU.
    Rev Med Brux; 1999 Dec 28; 20(6):495-503. PubMed ID: 10672773
    [Abstract] [Full Text] [Related]

  • 6. [SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
    Tang B, Wang D, Xia J.
    Zhonghua Yi Xue Za Zhi; 1997 Nov 28; 77(11):819-22. PubMed ID: 9772474
    [Abstract] [Full Text] [Related]

  • 7. Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients.
    Lopes-Cendes I, Teive HG, Calcagnotto ME, Da Costa JC, Cardoso F, Viana E, Maciel JA, Radvany J, Arruda WO, Trevisol-Bittencourt PC, Rosa Neto P, Silveira I, Steiner CE, Pinto Júnior W, Santos AS, Correa Neto Y, Werneck LC, Araújo AQ, Carakushansky G, Mello LR, Jardim LB, Rouleau GA.
    Arq Neuropsiquiatr; 1997 Sep 28; 55(3B):519-29. PubMed ID: 9629399
    [Abstract] [Full Text] [Related]

  • 8. Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.
    Ikeuchi T, Takano H, Koide R, Horikawa Y, Honma Y, Onishi Y, Igarashi S, Tanaka H, Nakao N, Sahashi K, Tsukagoshi H, Inoue K, Takahashi H, Tsuji S.
    Ann Neurol; 1997 Dec 28; 42(6):879-84. PubMed ID: 9403480
    [Abstract] [Full Text] [Related]

  • 9. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.
    Matilla T, McCall A, Subramony SH, Zoghbi HY.
    Ann Neurol; 1995 Jul 28; 38(1):68-72. PubMed ID: 7611728
    [Abstract] [Full Text] [Related]

  • 10. [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 28; 26(6):626-33. PubMed ID: 19953483
    [Abstract] [Full Text] [Related]

  • 11. 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 28; 39(4):490-9. PubMed ID: 8619527
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  • 13. [Clinico-genetic study of type I spinocerebelllar ataxia].
    Svetel M, Culjković B, Sternić N, Dragasević B, Stojković I, Romac S, Kostić VS.
    Srp Arh Celok Lek; 1999 Apr 28; 127(5-6):157-62. PubMed ID: 10500422
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  • 16. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
    Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H.
    Arch Neurol; 2004 Feb 28; 61(2):209-12. PubMed ID: 14967767
    [Abstract] [Full Text] [Related]

  • 17. Molecular genetics of hereditary ataxias.
    Banfi S, Zoghbi HY.
    Baillieres Clin Neurol; 1994 Aug 28; 3(2):281-95. PubMed ID: 7952848
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