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T Kitamoto

Showing results (71-80 of 183) with videos related to

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Neurology|February 1, 1996
Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodentsJ Tateishi, T Kitamoto, M Z Hoque, et al.
Rinsho Shinkeigaku = Clinical Neurology|November 1, 1996
[A case of Creutzfeldt-Jakob disease (CJD) started with monoparesis of the left arm]T Obi, M Takatsu, T Kitamoto, et al.
Rinsho Shinkeigaku = Clinical Neurology|June 1, 1994
[Creutzfeldt-Jakob disease with a point mutation at codon 232 of prion protein--a case report]T Shimizu, K Tanaka, N Tanahashi, et al.
Lancet (London, England)|January 7, 1995
Apolipoprotein E in Creutzfeldt-Jakob diseaseY Nakagawa, T Kitamoto, H Furukawa, et al.
Bioscience Reports|May 1, 1986
Scrapie-associated fibrils (SAF) purification method yields amyloid proteins from systemic and cerebral amyloidosisT Kitamoto, K Hikita, T Tashima, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|June 1, 1984
[Bulbospinal muscular atrophy with endocrinological abnormalities (Kennedy-Alter-Sung syndrome), with special reference to hypothalamo-pituitary dysfunction]T Kitamoto, R Kakigi, Y Kuroda, et al.
Journal of Neurobiology|January 20, 2000
Isolation and characterization of mutants for the vesicular acetylcholine transporter gene in Drosophila melanogasterT Kitamoto, X Xie, C F Wu, et al.
Rinsho Shinkeigaku = Clinical Neurology|September 1, 1983
[Case of alexia with agraphia caused by hematoma of the right temporal lobe]R Neshige, Y Kuroda, R Kakigi, et al.
Neuroscience Letters|March 10, 1995
Allelic variation of apolipoprotein E in Japanese sporadic Creutzfeldt-Jakob disease patientsY Nakagawa, T Kitamoto, H Furukawa, et al.
Brain Research|April 5, 1991
N-terminal sequence of prion protein is also integrated into kuru plaques in patients with Gerstmann-Sträussler syndromeT Kitamoto, T Muramoto, C Hilbich, et al.
Pageof 19

Showing results (71-80 of 183) with videos related to

Sort By:
Pageof 19
Neurology|February 1, 1996
Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodentsJ Tateishi, T Kitamoto, M Z Hoque, et al.
Rinsho Shinkeigaku = Clinical Neurology|November 1, 1996
[A case of Creutzfeldt-Jakob disease (CJD) started with monoparesis of the left arm]T Obi, M Takatsu, T Kitamoto, et al.
Rinsho Shinkeigaku = Clinical Neurology|June 1, 1994
[Creutzfeldt-Jakob disease with a point mutation at codon 232 of prion protein--a case report]T Shimizu, K Tanaka, N Tanahashi, et al.
Lancet (London, England)|January 7, 1995
Apolipoprotein E in Creutzfeldt-Jakob diseaseY Nakagawa, T Kitamoto, H Furukawa, et al.
Bioscience Reports|May 1, 1986
Scrapie-associated fibrils (SAF) purification method yields amyloid proteins from systemic and cerebral amyloidosisT Kitamoto, K Hikita, T Tashima, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|June 1, 1984
[Bulbospinal muscular atrophy with endocrinological abnormalities (Kennedy-Alter-Sung syndrome), with special reference to hypothalamo-pituitary dysfunction]T Kitamoto, R Kakigi, Y Kuroda, et al.
Journal of Neurobiology|January 20, 2000
Isolation and characterization of mutants for the vesicular acetylcholine transporter gene in Drosophila melanogasterT Kitamoto, X Xie, C F Wu, et al.
Rinsho Shinkeigaku = Clinical Neurology|September 1, 1983
[Case of alexia with agraphia caused by hematoma of the right temporal lobe]R Neshige, Y Kuroda, R Kakigi, et al.
Neuroscience Letters|March 10, 1995
Allelic variation of apolipoprotein E in Japanese sporadic Creutzfeldt-Jakob disease patientsY Nakagawa, T Kitamoto, H Furukawa, et al.
Brain Research|April 5, 1991
N-terminal sequence of prion protein is also integrated into kuru plaques in patients with Gerstmann-Sträussler syndromeT Kitamoto, T Muramoto, C Hilbich, et al.
Pageof 19