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T Kitamoto

Showing results (161-170 of 183) with videos related to

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Neurology|December 30, 2009
Discordant clinicopathologic phenotypes in a Japanese kindred of fatal familial insomniaY Saitoh, M Ogawa, Y Naito, et al.
Neuropathology and Applied Neurobiology|February 13, 2003
An atypical form of sporadic panencephalopathic Creutzfeldt-Jakob disease in JapanS Yamamoto, H Furukawa, T Kitamoto, et al.
Neurology|October 1, 1990
Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Sträussler-Scheinker syndromeJ Tateishi, T Kitamoto, K Doh-ura, et al.
Archives of Neurology|April 6, 1999
Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater graftingS Shimizu, K Hoshi, T Muramoto, et al.
Neurology|February 12, 2004
Clinical features of Creutzfeldt-Jakob disease with V180I mutationK Jin, Y Shiga, S Shibuya, et al.
Neurology|December 1, 1993
A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker diseaseM Yamada, Y Itoh, H Fujigasaki, et al.
Journal of Human Genetics|July 14, 2001
Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase familiesA Iida, S Saito, A Sekine, et al.
Neurology|February 13, 2003
Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaquesC Ishida, A Kakishima, S Okino, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 15, 1994
TNF-beta produced by human T lymphotropic virus type I-infected cells influences the proliferation of human endothelial cells and fibroblastsF Yu, Y Itoyama, J Kira, et al.
Acta Neuropathologica|January 1, 1995
Prion disease with 144 base pair insertion in a Japanese family lineT Oda, T Kitamoto, J Tateishi, et al.
Pageof 19

Showing results (161-170 of 183) with videos related to

Sort By:
Pageof 19
Neurology|December 30, 2009
Discordant clinicopathologic phenotypes in a Japanese kindred of fatal familial insomniaY Saitoh, M Ogawa, Y Naito, et al.
Neuropathology and Applied Neurobiology|February 13, 2003
An atypical form of sporadic panencephalopathic Creutzfeldt-Jakob disease in JapanS Yamamoto, H Furukawa, T Kitamoto, et al.
Neurology|October 1, 1990
Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Sträussler-Scheinker syndromeJ Tateishi, T Kitamoto, K Doh-ura, et al.
Archives of Neurology|April 6, 1999
Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater graftingS Shimizu, K Hoshi, T Muramoto, et al.
Neurology|February 12, 2004
Clinical features of Creutzfeldt-Jakob disease with V180I mutationK Jin, Y Shiga, S Shibuya, et al.
Neurology|December 1, 1993
A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker diseaseM Yamada, Y Itoh, H Fujigasaki, et al.
Journal of Human Genetics|July 14, 2001
Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase familiesA Iida, S Saito, A Sekine, et al.
Neurology|February 13, 2003
Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaquesC Ishida, A Kakishima, S Okino, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 15, 1994
TNF-beta produced by human T lymphotropic virus type I-infected cells influences the proliferation of human endothelial cells and fibroblastsF Yu, Y Itoyama, J Kira, et al.
Acta Neuropathologica|January 1, 1995
Prion disease with 144 base pair insertion in a Japanese family lineT Oda, T Kitamoto, J Tateishi, et al.
Pageof 19