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E Uyama

Showing results (1-10 of 91) with videos related to

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Ryoikibetsu Shokogun Shirizu|September 15, 2001
[Oculopharyngeal muscular dystrophy(OPMD)/oculopharyngeal myopathy]E Uyama
Rinsho Shinkeigaku = Clinical Neurology|January 1, 1992
[Some questions and comments for the original article entitled "autosomal recessive oculopharyngeal 'muscular dystrophy'"]E Uyama
Neurology|September 12, 2000
Gaucher disease with oculomotor apraxia and cardiovascular calcificationE Uyama
Ryoikibetsu Shokogun Shirizu|October 13, 2001
[Scapuloperoneal syndrome]E Uyama
Ryoikibetsu Shokogun Shirizu|October 13, 2001
[Oculopharyngodistal myopathy]M Uchino, E Uyama
Journal of the Neurological Sciences|December 1, 1996
Exacerbation of myasthenia gravis during interferon-alpha treatmentE Uyama, N Fujiki, M Uchino
Rinsho Shinkeigaku = Clinical Neurology|June 23, 1999
[Identification of Notch 3 mutation in the first Japanese CADASIL family]E Uyama, M Uchino, T Tabira
Neurology|November 1, 1995
Balint's syndromeE Uyama, M Uchino, M Ando
Journal of Neurology|March 1, 1996
Comments on "type 3 GM1 gangliosidosis: clinical and neuroradiological findings in an 11-year-old girl"E Uyama, M Uchino, M Ando
Annals of the New York Academy of Sciences|December 14, 2002
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and CADASIL-like disorders in JapanM Uchino, T Hirano, E Uyama, et al.
Pageof 10

Showing results (1-10 of 91) with videos related to

Sort By:
Pageof 10
Ryoikibetsu Shokogun Shirizu|September 15, 2001
[Oculopharyngeal muscular dystrophy(OPMD)/oculopharyngeal myopathy]E Uyama
Rinsho Shinkeigaku = Clinical Neurology|January 1, 1992
[Some questions and comments for the original article entitled "autosomal recessive oculopharyngeal 'muscular dystrophy'"]E Uyama
Neurology|September 12, 2000
Gaucher disease with oculomotor apraxia and cardiovascular calcificationE Uyama
Ryoikibetsu Shokogun Shirizu|October 13, 2001
[Scapuloperoneal syndrome]E Uyama
Ryoikibetsu Shokogun Shirizu|October 13, 2001
[Oculopharyngodistal myopathy]M Uchino, E Uyama
Journal of the Neurological Sciences|December 1, 1996
Exacerbation of myasthenia gravis during interferon-alpha treatmentE Uyama, N Fujiki, M Uchino
Rinsho Shinkeigaku = Clinical Neurology|June 23, 1999
[Identification of Notch 3 mutation in the first Japanese CADASIL family]E Uyama, M Uchino, T Tabira
Neurology|November 1, 1995
Balint's syndromeE Uyama, M Uchino, M Ando
Journal of Neurology|March 1, 1996
Comments on "type 3 GM1 gangliosidosis: clinical and neuroradiological findings in an 11-year-old girl"E Uyama, M Uchino, M Ando
Annals of the New York Academy of Sciences|December 14, 2002
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and CADASIL-like disorders in JapanM Uchino, T Hirano, E Uyama, et al.
Pageof 10