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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. Yoshida K, et al. Among authors: morita h. Cerebellum. 2009 Mar;8(1):46-51. doi: 10.1007/s12311-008-0062-8. Cerebellum. 2009. PMID: 18855094
Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study.
Nakamura K, Yoshida K, Matsushima A, Shimizu Y, Sato S, Yahikozawa H, Ohara S, Yazawa M, Ushiyama M, Sato M, Morita H, Inoue A, Ikeda SI. Nakamura K, et al. Among authors: morita h. Cerebellum. 2017 Apr;16(2):518-524. doi: 10.1007/s12311-016-0833-6. Cerebellum. 2017. PMID: 27830516
A Japanese case of SCA14 with the Gly128Asp mutation.
Morita H, Yoshida K, Suzuki K, Ikeda SI. Morita H, et al. J Hum Genet. 2006;51(12):1118-1121. doi: 10.1007/s10038-006-0063-8. Epub 2006 Sep 22. J Hum Genet. 2006. PMID: 17024314
[Dementia due to sarcoidosis].
Morita H, Ikeda S. Morita H, et al. Nihon Rinsho. 2004 Jan;62 Suppl:441-4. Nihon Rinsho. 2004. PMID: 15011402 Review. Japanese. No abstract available.
Adult or late-onset triple A syndrome: case report and literature review.
Nakamura K, Yoshida K, Yoshinaga T, Kodaira M, Shimojima Y, Takei Y, Morita H, Kayanuma K, Ikeda S. Nakamura K, et al. Among authors: morita h. J Neurol Sci. 2010 Oct 15;297(1-2):85-8. doi: 10.1016/j.jns.2010.07.006. Epub 2010 Aug 1. J Neurol Sci. 2010. PMID: 20674935 Review.
2,848 results