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Identification of a SACS gene missense mutation in ARSACS.
Ogawa T, Takiyama Y, Sakoe K, Mori K, Namekawa M, Shimazaki H, Nakano I, Nishizawa M. Ogawa T, et al. Neurology. 2004 Jan 13;62(1):107-9. doi: 10.1212/01.wnl.0000099371.14478.73. Neurology. 2004. PMID: 14718708
[Diabetic amyotrophy].
Ogawa T, Nakano I. Ogawa T, et al. Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):69-71. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11031897 Review. Japanese. No abstract available.
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. Ouyang Y, et al. Among authors: ogawa t. J Neurol Sci. 2006 Sep 25;247(2):180-6. doi: 10.1016/j.jns.2006.04.009. Epub 2006 Jun 15. J Neurol Sci. 2006. PMID: 16780885
Single sperm analysis of the CAG repeats in the gene for Machado-Joseph disease (MJD1): evidence for non-Mendelian transmission of the MJD1 gene and for the effect of the intragenic CGG/GGG polymorphism on the intergenerational instability.
Takiyama Y, Sakoe K, Soutome M, Namekawa M, Ogawa T, Nakano I, Igarashi S, Oyake M, Tanaka H, Tsuji S, Nishizawa M. Takiyama Y, et al. Among authors: ogawa t. Hum Mol Genet. 1997 Jul;6(7):1063-8. doi: 10.1093/hmg/6.7.1063. Hum Mol Genet. 1997. PMID: 9215676
A case of McLeod syndrome with unusually severe myopathy.
Kawakami T, Takiyama Y, Sakoe K, Ogawa T, Yoshioka T, Nishizawa M, Reid ME, Kobayashi O, Nonaka I, Nakano I. Kawakami T, et al. Among authors: ogawa t. J Neurol Sci. 1999 Jun 15;166(1):36-9. doi: 10.1016/s0022-510x(99)00108-2. J Neurol Sci. 1999. PMID: 10465497
5,904 results