M Uchino|E Uyama - JoVE Visualize

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Journal of the Neurological Sciences|June 1, 1995

Dentatorubral-pallidoluysian atrophy (DRPLA): clinical, genetic, and neuroradiologic studies in a familyE Uyama, I Kondo, M Uchino, et al.

Neuromuscular Disorders : NMD|August 6, 2003

A Japanese family with FEOM1-linked congenital fibrosis of the extraocular muscles type 1 associated with spinal canal stenosis and refinement of the FEOM1 critical regionE Uyama, K Yamada, H Kawano, et al.

Acta Neuropathologica|January 1, 1995

Polymerase chain reaction fiber analysis and somatic mosaicism in autopsied tissue from a man with Duchenne muscular dystrophyM Uchino, M Tokunaga, T Yamashita, et al.

Neuromuscular Disorders : NMD|December 10, 1997

Oculopharyngeal muscular dystrophy in JapanE Uyama, O Nohira, F M Tomé, et al.

Neuromuscular Disorders : NMD|January 5, 2000

Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotoniaR Sasaki, H Ichiyasu, N Ito, et al.

Rinsho Shinkeigaku = Clinical Neurology|July 24, 2001

[CADASIL: clinical analysis of CADASIL and CADASIL-like disorders in Japan]M Uchino, E Uyama, Y Maeda, et al.

The Tohoku Journal of Experimental Medicine|March 5, 2002

Clinical investigation of the lesions responsible for sensory disturbance in Minamata diseaseM Uchino, S Mita, H Satoh, et al.

Journal of Medical Genetics|January 1, 1996

Benign adult familial myoclonus epilepsy (BAFME): an autosomal dominant form not linked to the dentatorubral pallidoluysian atrophy (DRPLA) geneA Kuwano, F Takakubo, Y Morimoto, et al.

Journal of the Neurological Sciences|April 30, 1998

Adult Sandhoff's disease: R505Q and I207V substitutions in the HEXB gene of the first Japanese caseA Hara, E Uyama, M Uchino, et al.

Internal Medicine (Tokyo, Japan)|March 1, 1996

Distribution of dystrophin and dystrophin-associated protein 43DAG (beta-dystroglycan) in the central nervous system of normal controls and patients with Duchenne muscular dystrophyM Uchino, A Hara, Y Mizuno, et al.

Pageof 24

Showing results (31-40 of 236) with videos related to

Sort By:

Pageof 24

Journal of the Neurological Sciences|June 1, 1995

Dentatorubral-pallidoluysian atrophy (DRPLA): clinical, genetic, and neuroradiologic studies in a familyE Uyama, I Kondo, M Uchino, et al.

Neuromuscular Disorders : NMD|August 6, 2003

A Japanese family with FEOM1-linked congenital fibrosis of the extraocular muscles type 1 associated with spinal canal stenosis and refinement of the FEOM1 critical regionE Uyama, K Yamada, H Kawano, et al.

Acta Neuropathologica|January 1, 1995

Polymerase chain reaction fiber analysis and somatic mosaicism in autopsied tissue from a man with Duchenne muscular dystrophyM Uchino, M Tokunaga, T Yamashita, et al.

Neuromuscular Disorders : NMD|December 10, 1997

Oculopharyngeal muscular dystrophy in JapanE Uyama, O Nohira, F M Tomé, et al.

Neuromuscular Disorders : NMD|January 5, 2000

Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotoniaR Sasaki, H Ichiyasu, N Ito, et al.

Rinsho Shinkeigaku = Clinical Neurology|July 24, 2001

[CADASIL: clinical analysis of CADASIL and CADASIL-like disorders in Japan]M Uchino, E Uyama, Y Maeda, et al.

The Tohoku Journal of Experimental Medicine|March 5, 2002

Clinical investigation of the lesions responsible for sensory disturbance in Minamata diseaseM Uchino, S Mita, H Satoh, et al.

Journal of Medical Genetics|January 1, 1996

Benign adult familial myoclonus epilepsy (BAFME): an autosomal dominant form not linked to the dentatorubral pallidoluysian atrophy (DRPLA) geneA Kuwano, F Takakubo, Y Morimoto, et al.

Journal of the Neurological Sciences|April 30, 1998

Adult Sandhoff's disease: R505Q and I207V substitutions in the HEXB gene of the first Japanese caseA Hara, E Uyama, M Uchino, et al.

Internal Medicine (Tokyo, Japan)|March 1, 1996

Distribution of dystrophin and dystrophin-associated protein 43DAG (beta-dystroglycan) in the central nervous system of normal controls and patients with Duchenne muscular dystrophyM Uchino, A Hara, Y Mizuno, et al.

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