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Nihon Rinsho. Japanese Journal of Clinical Medicine|May 1, 1999
[Frequencies of triplet repeat disorders in dominantly inherited spinocerebellar ataxia (SCA) in the Japanese]H Sasaki, K TashiroCytogenetic and Genome Research|October 4, 2003
The hereditary spinocerebellar ataxias in JapanH Sasaki, I Yabe, K TashiroJournal of the Neurological Sciences|April 28, 2000
Prevalence of triplet repeat expansion in ataxia patients from Hokkaido, the northernmost island of JapanH Sasaki, I Yabe, I Yamashita, et al.No to Shinkei = Brain and Nerve|November 1, 1990
[A clinical study of a family affected with HLA-linked hereditary spinocerebellar ataxia]H Sasaki, T Hamada, A Wakisaka, et al.Psychiatry and Clinical Neurosciences|December 1, 1996
Serum carnitine and disabling fatigue in multiple sclerosisT Fukazawa, H Sasaki, S Kikuchi, et al.Rinsho Shinkeigaku = Clinical Neurology|December 16, 1998
[Periodic alternating nystagmus in spinocerebellar ataxia type 6 (SCA 6)]I Yabe, H Sasaki, I Yamashita, et al.Neurology|July 1, 1987
Skeletal myoclonus in olivopontocerebellar atrophy: treatment with trihexyphenidylH Sasaki, K Sudoh, K Hamada, et al.Rinsho Shinkeigaku = Clinical Neurology|November 1, 1991
[Clinical study of gene locus heterogeneity in hereditary olivopontocerebellar atrophy (OPCA)--report of 2 pedigrees affected with non SCA1 type OPCA]H Sasaki, A Wakisaka, K Tashiro, et al.Rinsho Shinkeigaku = Clinical Neurology|January 1, 1992
[Linkage study of hereditary olivopontocerebellar atrophy: genetic evidence for locus heterogeneity in Japanese cases]H Sasaki, A Wakisaka, K Tashiro, et al.Rinsho Shinkeigaku = Clinical Neurology|January 1, 1992
[Linkage study of Machado-Joseph disease: genetic evidence for the locus different from SCA1]H Sasaki, A Wakisaka, K Tashiro, et al.Pageof 234