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

233 related items for PubMed ID: 16780885

  • 1. 16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.
    Ouyang Y, Sakoe K, Shimazaki H, Namekawa M, Ogawa T, Ando Y, Kawakami T, Kaneko J, Hasegawa Y, Yoshizawa K, Amino T, Ishikawa K, Mizusawa H, Nakano I, Takiyama Y.
    J Neurol Sci; 2006 Sep 25; 247(2):180-6. PubMed ID: 16780885
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan.
    Hirano R, Takashima H, Okubo R, Okamoto Y, Maki Y, Ishida S, Suehara M, Hokezu Y, Arimura K.
    J Hum Genet; 2009 Jul 30; 54(7):377-81. PubMed ID: 19444286
    [Abstract] [Full Text] [Related]

  • 5. 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 30; 116(2):123-7. PubMed ID: 17661799
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. 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 30; 77(2):280-96. PubMed ID: 16001362
    [Abstract] [Full Text] [Related]

  • 9. A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.
    Owada K, Ishikawa K, Toru S, Ishida G, Gomyoda M, Tao O, Noguchi Y, Kitamura K, Kondo I, Noguchi E, Arinami T, Mizusawa H.
    Neurology; 2005 Aug 23; 65(4):629-32. PubMed ID: 16116133
    [Abstract] [Full Text] [Related]

  • 10. 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 Aug 23; 52(8):643-649. PubMed ID: 17611710
    [Abstract] [Full Text] [Related]

  • 11. Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.
    Li M, Ishikawa K, Toru S, Tomimitsu H, Takashima M, Goto J, Takiyama Y, Sasaki H, Imoto I, Inazawa J, Toda T, Kanazawa I, Mizusawa H.
    J Hum Genet; 2003 Aug 23; 48(3):111-8. PubMed ID: 12624721
    [Abstract] [Full Text] [Related]

  • 12. 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 Aug 23; 51(5):461-466. PubMed ID: 16614795
    [Abstract] [Full Text] [Related]

  • 13. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I.
    Benomar A, Le Guern E, Dürr A, Ouhabi H, Stevanin G, Yahyaoui M, Chkili T, Agid Y, Brice A.
    Ann Neurol; 1994 Apr 23; 35(4):439-44. PubMed ID: 8154871
    [Abstract] [Full Text] [Related]

  • 14. 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 23; 5(4):215-21. PubMed ID: 15455264
    [Abstract] [Full Text] [Related]

  • 15. A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan.
    Takashima M, Ishikawa K, Nagaoka U, Shoji S, Mizusawa H.
    J Hum Genet; 2001 Dec 23; 46(4):167-71. PubMed ID: 11322654
    [Abstract] [Full Text] [Related]

  • 16. The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell: The 50th Anniversary of Japanese Society of Neuropathology.
    Ishikawa K, Mizusawa H.
    Neuropathology; 2010 Oct 23; 30(5):490-4. PubMed ID: 20667009
    [Abstract] [Full Text] [Related]

  • 17. [Autosomal dominant cortical cerebellar atrophy (ADCCA) linked to chromosome 16q].
    Ishikawa K.
    Rinsho Shinkeigaku; 2001 Dec 23; 41(12):1117-9. PubMed ID: 12235813
    [Abstract] [Full Text] [Related]

  • 18. 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 23; 51(4):363-367. PubMed ID: 16491300
    [Abstract] [Full Text] [Related]

  • 19. Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.
    Verbeek DS, Schelhaas JH, Ippel EF, Beemer FA, Pearson PL, Sinke RJ.
    Hum Genet; 2002 Oct 23; 111(4-5):388-93. PubMed ID: 12384780
    [Abstract] [Full Text] [Related]

  • 20. Cerebellar ataxia with spasmodic cough: a new form of dominant ataxia.
    Coutinho P, Cruz VT, Tuna A, Silva SE, Guimarães J.
    Arch Neurol; 2006 Apr 23; 63(4):553-5. PubMed ID: 16606768
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.