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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

153 related items for PubMed ID: 18293026

  • 1. Spinocerebellar ataxia type 4 and 16q22.1-linked Japanese ataxia are not allelic.
    Hellenbroich Y, Bernard V, Zühlke C.
    J Neurol; 2008 Apr; 255(4):612-3. PubMed ID: 18293026
    [No Abstract] [Full Text] [Related]

  • 2. An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.
    Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H.
    Am J Hum Genet; 2005 Aug; 77(2):280-96. PubMed ID: 16001362
    [Abstract] [Full Text] [Related]

  • 3. The (-16C > T) substitution in the PLEKHG4 gene is not present among European ADCA patients.
    Cagnoli C, Brussino A, Di Gregorio E, Brusco A, Stevanin G, Durr A, Brice A.
    Mov Disord; 2007 Apr 15; 22(5):752-3. PubMed ID: 17290458
    [No Abstract] [Full Text] [Related]

  • 4. Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan.
    Hayashi M, Adachi Y, Mori M, Nakano T, Nakashima K.
    Acta Neurol Scand; 2007 Aug 15; 116(2):123-7. PubMed ID: 17661799
    [Abstract] [Full Text] [Related]

  • 5. New gene of spinocerebellar ataxia.
    Teive HA, Munhoz RP, Ashizawa T.
    Brain; 2011 Jul 15; 134(Pt 7):e179. PubMed ID: 21357611
    [No Abstract] [Full Text] [Related]

  • 6. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese.
    Onodera Y, Aoki M, Mizuno H, Warita H, Shiga Y, Itoyama Y.
    Neurology; 2006 Oct 10; 67(7):1300-2. PubMed ID: 17030774
    [Abstract] [Full Text] [Related]

  • 7. Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.
    Nozaki H, Ikeuchi T, Kawakami A, Kimura A, Koide R, Tsuchiya M, Nakmura Y, Mutoh T, Yamamoto H, Nakao N, Sahashi K, Nishizawa M, Onodera O.
    Mov Disord; 2007 Apr 30; 22(6):857-62. PubMed ID: 17357132
    [Abstract] [Full Text] [Related]

  • 8. Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.
    Hirano R, Takashima H, Okubo R, Tajima K, Okamoto Y, Ishida S, Tsuruta K, Arisato T, Arata H, Nakagawa M, Osame M, Arimura K.
    Neurogenetics; 2004 Dec 30; 5(4):215-21. PubMed ID: 15455264
    [Abstract] [Full Text] [Related]

  • 9. Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.
    Amino T, Ishikawa K, Toru S, Ishiguro T, Sato N, Tsunemi T, Murata M, Kobayashi K, Inazawa J, Toda T, Mizusawa H.
    J Hum Genet; 2007 Dec 30; 52(8):643-649. PubMed ID: 17611710
    [Abstract] [Full Text] [Related]

  • 10. Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population.
    Wieczorek S, Arning L, Alheite I, Epplen JT.
    J Hum Genet; 2006 Dec 30; 51(4):363-367. PubMed ID: 16491300
    [Abstract] [Full Text] [Related]

  • 11. [Study on the single-nucleotide substitution (c.-16C to T) of the PURATROPHIN-1 gene in Chinese patients with spinocerebellar ataxia].
    Zhou Y, Song X, Yi J, Jiang H, Wang J, Liao S, Tang B.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec 30; 25(6):646-8. PubMed ID: 19065522
    [Abstract] [Full Text] [Related]

  • 12. 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 30; 58(5):789-94. PubMed ID: 11346374
    [Abstract] [Full Text] [Related]

  • 13. Predisposing chromosome for spinocerebellar ataxia type 6 (SCA6) in Japanese.
    Yabe I, Sasaki H, Yamashita I, Tashiro K, Takei A, Suzuki Y, Kida H, Takiyama Y, Nishizawa M, Hokezu Y, Nagamatsu K, Oda T, Ohnishi A, Inoue I, Hata A.
    J Med Genet; 2001 May 30; 38(5):328-33. PubMed ID: 11403042
    [No Abstract] [Full Text] [Related]

  • 14. [Molecular genetic approach to spinocerebellar ataxias].
    Ishikawa K, Ishiguro T, Takahashi M, Sato N, Amino T, Niimi Y, Mizusawa H.
    Rinsho Shinkeigaku; 2009 Nov 30; 49(11):907-9. PubMed ID: 20030245
    [Abstract] [Full Text] [Related]

  • 15. A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.
    Ohata T, Yoshida K, Sakai H, Hamanoue H, Mizuguchi T, Shimizu Y, Okano T, Takada F, Ishikawa K, Mizusawa H, Yoshiura KI, Fukushima Y, Ikeda SI, Matsumoto N.
    J Hum Genet; 2006 Nov 30; 51(5):461-466. PubMed ID: 16614795
    [Abstract] [Full Text] [Related]

  • 16. TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
    Wang JL, Yang X, Xia K, Hu ZM, Weng L, Jin X, Jiang H, Zhang P, Shen L, Guo JF, Li N, Li YR, Lei LF, Zhou J, Du J, Zhou YF, Pan Q, Wang J, Wang J, Li RQ, Tang BS.
    Brain; 2010 Dec 30; 133(Pt 12):3510-8. PubMed ID: 21106500
    [Abstract] [Full Text] [Related]

  • 17. Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
    Hiramoto K, Kawakami H, Inoue K, Seki T, Maruyama H, Morino H, Matsumoto M, Kurisu K, Sakai N.
    Mov Disord; 2006 Sep 30; 21(9):1355-60. PubMed ID: 16763984
    [Abstract] [Full Text] [Related]

  • 18. Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan.
    Sakai H, Yoshida K, Shimizu Y, Morita H, Ikeda S, Matsumoto N.
    Neurogenetics; 2010 Oct 30; 11(4):409-15. PubMed ID: 20424877
    [Abstract] [Full Text] [Related]

  • 19. [Spinocerebellar ataxia type 31].
    Ishikawa K, Sato N, Niimi Y, Amino T, Mizusawa H.
    Rinsho Shinkeigaku; 2010 Nov 30; 50(11):985-7. PubMed ID: 21921537
    [Abstract] [Full Text] [Related]

  • 20. Two dominantly inherited ataxias linked to chromosome 16q22.1: SCA4 and SCA31 are not allelic.
    Edener U, Bernard V, Hellenbroich Y, Gillessen-Kaesbach G, Zühlke C.
    J Neurol; 2011 Jul 30; 258(7):1223-7. PubMed ID: 21267591
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.