Doh-ura K - Search Results

1

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. Neurology. 1994 Feb;44(2):299-301. doi: 10.1212/wnl.44.2.299. Neurology. 1994. PMID: 7906019

2

Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations.

Miyazono M, Kitamoto T, Doh-ura K, Iwaki T, Tateishi J. Miyazono M, et al. Acta Neuropathol. 1992;84(4):349-54. doi: 10.1007/BF00227660. Acta Neuropathol. 1992. PMID: 1359725

3

A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann-Sträussler syndrome.

Kitamoto T, Yamaguchi K, Doh-ura K, Tateishi J. Kitamoto T, et al. Neurology. 1991 Feb;41(2 ( Pt 1)):306-10. doi: 10.1212/wnl.41.2_part_1.306. Neurology. 1991. PMID: 1671530

4

Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease.

Kitamoto T, Muramoto T, Mohri S, Doh-Ura K, Tateishi J. Kitamoto T, et al. J Virol. 1991 Nov;65(11):6292-5. doi: 10.1128/JVI.65.11.6292-6295.1991. J Virol. 1991. PMID: 1681118 Free PMC article.

5

Clustering of three cases of Creutzfeldt-Jakob disease near Fukuoka City, Japan.

Arakawa K, Nagara H, Itoyama Y, Doh-ura K, Tomokane N, Tateishi J, Goto I. Arakawa K, et al. Acta Neurol Scand. 1991 Nov;84(5):445-7. doi: 10.1111/j.1600-0404.1991.tb04986.x. Acta Neurol Scand. 1991. PMID: 1685612

6

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Sträussler-Scheinker syndrome.

Tateishi J, Kitamoto T, Doh-ura K, Sakaki Y, Steinmetz G, Tranchant C, Warter JM, Heldt N. Tateishi J, et al. Neurology. 1990 Oct;40(10):1578-81. doi: 10.1212/wnl.40.10.1578. Neurology. 1990. PMID: 1699173

7

Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome.

Doh-ura K, Tateishi J, Kitamoto T, Sasaki H, Sakaki Y. Doh-ura K, et al. Ann Neurol. 1990 Feb;27(2):121-6. doi: 10.1002/ana.410270205. Ann Neurol. 1990. PMID: 2180366

8

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome.

Kitamoto T, Ohta M, Doh-ura K, Hitoshi S, Terao Y, Tateishi J. Kitamoto T, et al. Biochem Biophys Res Commun. 1993 Mar 15;191(2):709-14. doi: 10.1006/bbrc.1993.1275. Biochem Biophys Res Commun. 1993. PMID: 8461023

9

[Prion diseases and a new variant of Creutzfeldt-Jakob disease].

Doh-ura K, Kitamoto T. Doh-ura K, et al. Rinsho Shinkeigaku. 1996 Dec;36(12):1370-2. Rinsho Shinkeigaku. 1996. PMID: 9128415 Japanese.

10

Clinical features of Creutzfeldt-Jakob disease with V180I mutation.

Jin K, Shiga Y, Shibuya S, Chida K, Sato Y, Konno H, Doh-ura K, Kitamoto T, Itoyama Y. Jin K, et al. Neurology. 2004 Feb 10;62(3):502-5. doi: 10.1212/01.wnl.0000106954.54011.80. Neurology. 2004. PMID: 14872044

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