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Journal Abstract Search

232 related items for PubMed ID: 9847664

  • 21. Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
    Schöls L, Krüger R, Amoiridis G, Przuntek H, Epplen JT, Riess O.
    J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):67-73. PubMed ID: 9436730
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  • 22. [Spinocerebellar ataxias in infancy: pathogenesis of potassium and calcium channels' diseases, clinical features and therapeutical approach].
    Bozzola E, Savasta S, Peruzzi C, Bozzola M, Bona G.
    Minerva Pediatr; 2007 Apr; 59(2):149-56. PubMed ID: 17404565
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  • 23. 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; 61(2):209-12. PubMed ID: 14967767
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  • 24. Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).
    Matsuyama Z, Kawakami H, Maruyama H, Izumi Y, Komure O, Udaka F, Kameyama M, Nishio T, Kuroda Y, Nishimura M, Nakamura S.
    Hum Mol Genet; 1997 Aug; 6(8):1283-7. PubMed ID: 9259274
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  • 25. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
    Zhuchenko O, Bailey J, Bonnen P, Ashizawa T, Stockton DW, Amos C, Dobyns WB, Subramony SH, Zoghbi HY, Lee CC.
    Nat Genet; 1997 Jan; 15(1):62-9. PubMed ID: 8988170
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  • 27. Genetics of the SCA6 gene in a large family segregating an autosomal dominant "pure" cerebellar ataxia.
    García-Planells J, Cuesta A, Vilchez JJ, Martínez F, Prieto F, Palau F.
    J Med Genet; 1999 Feb; 36(2):148-51. PubMed ID: 10051016
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  • 28. Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6).
    Sasaki H, Kojima H, Yabe I, Tashiro K, Hamada T, Sawa H, Hiraga H, Nagashima K.
    Acta Neuropathol; 1998 Feb; 95(2):199-204. PubMed ID: 9498057
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  • 31. [A case of spinocerebellar ataxia 6 accompanied with schizophrenia].
    Nakanishi I, Miwa H, Hayata T, Kawada A, Kondo T.
    No To Shinkei; 2004 Jan; 56(1):49-52. PubMed ID: 15024829
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  • 32. SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene.
    Riess O, Schöls L, Bottger H, Nolte D, Vieira-Saecker AM, Schimming C, Kreuz F, Macek M, Krebsová A, Macek M Sen, Klockgether T, Zühlke C, Laccone FA.
    Hum Mol Genet; 1997 Aug; 6(8):1289-93. PubMed ID: 9259275
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  • 33. A Japanese family with spinocerebellar ataxia type 6 which includes three individuals homozygous for an expanded CAG repeat in the SCA6/CACNL1A4 gene.
    Takiyama Y, Sakoe K, Namekawa M, Soutome M, Esumi E, Ogawa T, Ishikawa K, Mizusawa H, Nakano I, Nishizawa M.
    J Neurol Sci; 1998 Jun 30; 158(2):141-7. PubMed ID: 9702684
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  • 34. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
    Yu GY, Howell MJ, Roller MJ, Xie TD, Gomez CM.
    Ann Neurol; 2005 Mar 30; 57(3):349-54. PubMed ID: 15732118
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  • 36. Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.
    Ishikawa K, Tanaka H, Saito M, Ohkoshi N, Fujita T, Yoshizawa K, Ikeuchi T, Watanabe M, Hayashi A, Takiyama Y, Nishizawa M, Nakano I, Matsubayashi K, Miwa M, Shoji S, Kanazawa I, Tsuji S, Mizusawa H.
    Am J Hum Genet; 1997 Aug 30; 61(2):336-46. PubMed ID: 9311738
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  • 37. Spinocerebellar ataxia type 6.
    Solodkin A, Gomez CM.
    Handb Clin Neurol; 2012 Aug 30; 103():461-73. PubMed ID: 21827907
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  • 38. [Siblings with spinocerebellar ataxia type 1 (SCA 1)--diagnosis by detecting the expansion of CAG repeat on chromosome 6p].
    Hanihara T, Takahashi T, Inoue K, Yamada Y, Iwabuchi K.
    Rinsho Shinkeigaku; 1994 May 30; 34(5):508-10. PubMed ID: 7924069
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