Kitamoto T - Search Results

1

The risk of iatrogenic Creutzfeldt-Jakob disease through medical and surgical procedures.

Hamaguchi T, Noguchi-Shinohara M, Nozaki I, Nakamura Y, Sato T, Kitamoto T, Mizusawa H, Yamada M. Hamaguchi T, et al. Among authors: kitamoto t. Neuropathology. 2009 Oct;29(5):625-31. doi: 10.1111/j.1440-1789.2009.01023.x. Epub 2009 Jul 29. Neuropathology. 2009. PMID: 19659942 Review.

2

[An autopsy-verified case of Creutzfeldt-Jakob disease with codon 129 polymorphism and codon 180 point mutation].

Matsumura T, Kojima S, Kuroiwa Y, Takagi A, Unakami M, Kitamoto T. Matsumura T, et al. Among authors: kitamoto t. Rinsho Shinkeigaku. 1995 Mar;35(3):282-5. Rinsho Shinkeigaku. 1995. PMID: 7614752 Japanese.

3

Allelic variation of apolipoprotein E in Japanese sporadic Creutzfeldt-Jakob disease patients.

Nakagawa Y, Kitamoto T, Furukawa H, Ogomori K, Tateishi J. Nakagawa Y, et al. Among authors: kitamoto t. Neurosci Lett. 1995 Mar 10;187(3):209-11. doi: 10.1016/0304-3940(95)11366-5. Neurosci Lett. 1995. PMID: 7624027

4

A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease.

Yamada M, Itoh Y, Fujigasaki H, Naruse S, Kaneko K, Kitamoto T, Tateishi J, Otomo E, Hayakawa M, Tanaka J, et al. Yamada M, et al. Among authors: kitamoto t. Neurology. 1993 Dec;43(12):2723-4. doi: 10.1212/wnl.43.12.2723-a. Neurology. 1993. PMID: 7902972 No abstract available.

5

Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene.

Inoue I, Kitamoto T, Doh-ura K, Shii H, Goto I, Tateishi J. Inoue I, et al. Among authors: kitamoto t. Neurology. 1994 Feb;44(2):299-301. doi: 10.1212/wnl.44.2.299. Neurology. 1994. PMID: 7906019

6

[Creutzfeldt-Jakob disease with a point mutation at codon 232 of prion protein--a case report].

Shimizu T, Tanaka K, Tanahashi N, Fukuuchi Y, Kitamoto T. Shimizu T, et al. Among authors: kitamoto t. Rinsho Shinkeigaku. 1994 Jun;34(6):590-2. Rinsho Shinkeigaku. 1994. PMID: 7955719 Japanese.

7

Double mutations at codon 180 and codon 232 of the PRNP gene in an apparently sporadic case of Creutzfeldt-Jakob disease.

Hitoshi S, Nagura H, Yamanouchi H, Kitamoto T. Hitoshi S, et al. Among authors: kitamoto t. J Neurol Sci. 1993 Dec 15;120(2):208-12. doi: 10.1016/0022-510x(93)90275-4. J Neurol Sci. 1993. PMID: 8138811

8

Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents.

Tateishi J, Kitamoto T, Hoque MZ, Furukawa H. Tateishi J, et al. Among authors: kitamoto t. Neurology. 1996 Feb;46(2):532-7. doi: 10.1212/wnl.46.2.532. Neurology. 1996. PMID: 8614527

9

A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210.

Furukawa H, Kitamoto T, Hashiguchi H, Tateishi J. Furukawa H, et al. Among authors: kitamoto t. J Neurol Sci. 1996 Sep 15;141(1-2):120-2. doi: 10.1016/0022-510x(96)00157-8. J Neurol Sci. 1996. PMID: 8880705

10

Immunhistological evaluation of Creutzfeldt-Jakob disease with reference to the type PrPres deposition.

Tateishi J, Kitamoto T, Kretzschmar H, Mehraein P. Tateishi J, et al. Among authors: kitamoto t. Clin Neuropathol. 1996 Nov-Dec;15(6):358-60. Clin Neuropathol. 1996. PMID: 8937784

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