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100 related items for PubMed ID: 19444286
1. 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; 54(7):377-81. PubMed ID: 19444286 [Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
6. 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 Oct 10; 48(3):111-8. PubMed ID: 12624721 [Abstract] [Full Text] [Related]
7. 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 Oct 10; 46(4):167-71. PubMed ID: 11322654 [Abstract] [Full Text] [Related]
8. Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of Japan. Yoshida K, Shimizu Y, Morita H, Okano T, Sakai H, Ohata T, Matsumoto N, Nakamura K, Tazawa K, Ohara S, Tabata K, Inoue A, Sato S, Shimojima Y, Hattori T, Ushiyama M, Ikeda S. Cerebellum; 2009 Mar 10; 8(1):46-51. PubMed ID: 18855094 [Abstract] [Full Text] [Related]
18. Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12. Sato K, Yabe I, Fukuda Y, Soma H, Nakahara Y, Tsuji S, Sasaki H. Arch Neurol; 2010 Oct 15; 67(10):1257-62. PubMed ID: 20937954 [Abstract] [Full Text] [Related]
20. Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families. Basri R, Yabe I, Soma H, Sasaki H. J Hum Genet; 2007 Oct 15; 52(10):848-855. PubMed ID: 17805477 [Abstract] [Full Text] [Related] Page: [Next] [New Search]