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Page 1
Ataxia with isolated vitamin E deficiency and retinitis pigmentosa.
Shimohata T, Date H, Ishiguro H, Suzuki T, Takano H, Tanaka H, Tsuji S, Hirota K. Shimohata T, et al. Among authors: ishiguro h. Ann Neurol. 1998 Feb;43(2):273. doi: 10.1002/ana.410430222. Ann Neurol. 1998. PMID: 9485073 No abstract available.
Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families.
Hara K, Shiga A, Nozaki H, Mitsui J, Takahashi Y, Ishiguro H, Yomono H, Kurisaki H, Goto J, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O. Hara K, et al. Among authors: ishiguro h. Neurology. 2008 Aug 19;71(8):547-51. doi: 10.1212/01.wnl.0000311277.71046.a0. Epub 2008 Jun 25. Neurology. 2008. PMID: 18579805
Pontine atrophy in spinocerebellar ataxia type 6.
Sugawara M, Toyoshima I, Wada C, Kato K, Ishikawa K, Hirota K, Ishiguro H, Kagaya H, Hirata Y, Imota T, Ogasawara M, Masamune O. Sugawara M, et al. Among authors: ishiguro h. Eur Neurol. 2000;43(1):17-22. doi: 10.1159/000008123. Eur Neurol. 2000. PMID: 10601803
[Hereditary ataxias in Akita prefecture].
Sugawara M, Toyoshima I, Kato K, Wada C, Imota T, Hirota K, Ishiguro H, Kagaya H, Hirata A, Ogasawara M, Masamune O. Sugawara M, et al. Among authors: ishiguro h. Rinsho Shinkeigaku. 1999 Jul;39(7):763-6. Rinsho Shinkeigaku. 1999. PMID: 10548917 Japanese.
924 results