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Journal Abstract Search
405 related items for PubMed ID: 9403480
1. 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; 42(6):879-84. PubMed ID: 9403480 [Abstract] [Full Text] [Related]
2. [Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese]. Ikeuchi T. Nihon Rinsho; 1999 Apr; 57(4):891-5. PubMed ID: 10222785 [Abstract] [Full Text] [Related]
3. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1. Hashida H, Goto J, Kurisaki H, Mizusawa H, Kanazawa I. Ann Neurol; 1997 Apr; 41(4):505-11. PubMed ID: 9124808 [Abstract] [Full Text] [Related]
4. [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]
8. 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]
9. [Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)]. Ishikawa K, Mizusawa H. Nihon Rinsho; 1999 Apr 30; 57(4):880-5. PubMed ID: 10222783 [Abstract] [Full Text] [Related]
14. [Spinocerebellar ataxia: advances in genetic research and its clinical implication]. Sasaki H. Hokkaido Igaku Zasshi; 1997 Jan 30; 72(1):13-20. PubMed ID: 9086358 [Abstract] [Full Text] [Related]
15. 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]