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Journal of the Neurological Sciences|October 1, 1994
Cognitive event-related potentials and brain magnetic resonance imaging in HTLV-1 associated myelopathy (HAM)T Fukushima, T Ikeda, E Uyama, et al.Alzheimer Disease and Associated Disorders|December 28, 1999
Identification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyK Kamimura, K Takahashi, E Uyama, et al.Headache|September 1, 1995
Headache associated with aseptic meningeal reaction as clinical onset of Fabry's diseaseE Uyama, N Ueno, M Uchino, et al.Muscle & Nerve|May 16, 2001
A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotonia congenitaR Sasaki, N Ito, M Shimamura, et al.Journal of the Neurological Sciences|July 1, 1994
PCR and immunoblot analyses of dystrophin in Becker muscular dystrophyM Uchino, T Miike, H Iwashita, et al.Stroke|June 1, 1989
Progressing ischemic stroke in a homozygote with variant antithrombin IIIH Ueyama, Y Hashimoto, M Uchino, et al.Internal Medicine (Tokyo, Japan)|March 1, 1995
Involvement of the central nervous system in rheumatoid arthritis: its clinical manifestations and analysis by magnetic resonance imagingY Ando, S Kai, E Uyama, et al.Internal Medicine (Tokyo, Japan)|September 2, 2000
Arg133Cys mutation of Notch3 in two unrelated Japanese families with CADASILE Uyama, M Tokunaga, A Suenaga, et al.Acta Neurologica Scandinavica|March 1, 1994
Adult Chédiak-Higashi syndrome presenting as parkinsonism and dementiaE Uyama, T Hirano, K Ito, et al.Neuroradiology|April 18, 2001
High signal in the spinal cord on T2-weighted images in rapidly progressive tropical spastic paraparesisM Watanabe, T Yamashita, A Hara, et al.Pageof 24