Similar articles for PMID: 8461023

Year	Number of Results
1986	1
1989	3
1990	8
1991	19
1992	12
1993	11
1994	13
1995	12
1996	13
1997	8
1998	8
1999	13
2000	14
2001	8
2002	5
2003	5
2004	5
2005	3
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2007	5
2008	9
2009	10
2010	9
2011	6
2012	6
2013	10
2014	5
2015	1
2016	3
2017	4
2018	3
2019	7
2020	4
2021	4
2022	5
2023	2
2024	0

1

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

2

[Molecular genetics in Creutzfeldt-Jakob disease].

Kitamoto T. Kitamoto T. Rinsho Shinkeigaku. 1994 Dec;34(12):1222-3. Rinsho Shinkeigaku. 1994. PMID: 7774117 Review. Japanese.

3

A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene.

Liberski PP, Barcikowska M, Cervenakova L, Bratosiewicz J, Marczewska M, Brown P, Gajdusek DC. Liberski PP, et al. Acta Neuropathol. 1998 Oct;96(4):425-30. doi: 10.1007/s004010050915. Acta Neuropathol. 1998. PMID: 9797009

4

New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome.

Furukawa H, Kitamoto T, Tanaka Y, Tateishi J. Furukawa H, et al. Brain Res Mol Brain Res. 1995 Jun;30(2):385-8. doi: 10.1016/0169-328x(95)00034-p. Brain Res Mol Brain Res. 1995. PMID: 7637591

5

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

6

Insertions in the prion protein gene in atypical dementias.

Owen F, Poulter M, Collinge J, Leach M, Shah T, Lofthouse R, Chen YF, Crow TJ, Harding AE, Hardy J, et al. Owen F, et al. Exp Neurol. 1991 May;112(2):240-2. doi: 10.1016/0014-4886(91)90075-n. Exp Neurol. 1991. PMID: 1674696

7

[Genetic background of human prion diseases].

Kovács GG. Kovács GG. Ideggyogy Sz. 2007 Nov 30;60(11-12):438-46. Ideggyogy Sz. 2007. PMID: 18198790 Review. Hungarian.

8

Detecting prion protein gene mutations by denaturing gradient gel electrophoresis.

Fink JK, Peacock ML, Warren JT Jr, Roses AD, Prusiner SB. Fink JK, et al. Hum Mutat. 1994;4(1):42-50. doi: 10.1002/humu.1380040106. Hum Mutat. 1994. PMID: 7951257 Free article.

9

An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques.

Kitamoto T, Iizuka R, Tateishi J. Kitamoto T, et al. Biochem Biophys Res Commun. 1993 Apr 30;192(2):525-31. doi: 10.1006/bbrc.1993.1447. Biochem Biophys Res Commun. 1993. PMID: 8097911

10

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

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