Similar articles for PMID: 21760536

Year	Number of Results
1980	1
1982	1
1986	1
1989	4
1990	4
1991	13
1992	11
1993	10
1994	8
1995	13
1996	6
1997	5
1998	8
1999	8
2000	9
2001	8
2002	2
2003	5
2004	2
2005	4
2006	6
2007	4
2008	8
2009	10
2010	11
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2012	9
2013	7
2014	8
2015	4
2016	14
2017	10
2018	9
2019	9
2020	9
2021	10
2022	6
2023	2
2024	0

1

A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.

Jansen C, Parchi P, Capellari S, Strammiello R, Dopper EG, van Swieten JC, Kamphorst W, Rozemuller AJ. Jansen C, et al. J Neuropathol Exp Neurol. 2011 Aug;70(8):698-702. doi: 10.1097/NEN.0b013e3182270c54. J Neuropathol Exp Neurol. 2011. PMID: 21760536

2

A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease.

Panegyres PK, Toufexis K, Kakulas BA, Cernevakova L, Brown P, Ghetti B, Piccardo P, Dlouhy SR. Panegyres PK, et al. Arch Neurol. 2001 Nov;58(11):1899-902. doi: 10.1001/archneur.58.11.1899. Arch Neurol. 2001. PMID: 11709001

3

Unusual clinical and molecular-pathological profile of gerstmann-Sträussler-Scheinker disease associated with a novel PRNP mutation (V176G).

Simpson M, Johanssen V, Boyd A, Klug G, Masters CL, Li QX, Pamphlett R, McLean C, Lewis V, Collins SJ. Simpson M, et al. JAMA Neurol. 2013 Sep 1;70(9):1180-5. doi: 10.1001/jamaneurol.2013.165. JAMA Neurol. 2013. PMID: 23857164

4

A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature.

Jansen C, Voet W, Head MW, Parchi P, Yull H, Verrips A, Wesseling P, Meulstee J, Baas F, van Gool WA, Ironside JW, Rozemuller AJ. Jansen C, et al. Acta Neuropathol. 2011 Jan;121(1):59-68. doi: 10.1007/s00401-010-0656-3. Epub 2010 Mar 3. Acta Neuropathol. 2011. PMID: 20198483 Free PMC article. Review.

5

[Gerstmann-Straüssler-Scheinker syndrome].

Tranchant C, Warter JM. Tranchant C, et al. Rev Neurol (Paris). 1998 Feb;154(2):152-7. Rev Neurol (Paris). 1998. PMID: 9773036 Review. French.

6

Hyperphosphorylated tau deposition parallels prion protein burden in a case of Gerstmann-Sträussler-Scheinker syndrome P102L mutation complicated with dementia.

Ishizawa K, Komori T, Shimazu T, Yamamoto T, Kitamoto T, Shimazu K, Hirose T. Ishizawa K, et al. Acta Neuropathol. 2002 Oct;104(4):342-50. doi: 10.1007/s00401-002-0547-3. Epub 2002 May 14. Acta Neuropathol. 2002. PMID: 12200619

7

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.

Hsiao K, Dlouhy SR, Farlow MR, Cass C, Da Costa M, Conneally PM, Hodes ME, Ghetti B, Prusiner SB. Hsiao K, et al. Nat Genet. 1992 Apr;1(1):68-71. doi: 10.1038/ng0492-68. Nat Genet. 1992. PMID: 1363810

8

Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits.

Colucci M, Moleres FJ, Xie ZL, Ray-Chaudhury A, Gutti S, Butefisch CM, Cervenakova L, Wang W, Goldfarb LG, Kong Q, Ghetti B, Chen SG, Gambetti P. Colucci M, et al. J Neuropathol Exp Neurol. 2006 Jul;65(7):642-51. doi: 10.1097/01.jnen.0000228198.81797.4d. J Neuropathol Exp Neurol. 2006. PMID: 16825951

9

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene.

Dlouhy SR, Hsiao K, Farlow MR, Foroud T, Conneally PM, Johnson P, Prusiner SB, Hodes ME, Ghetti B. Dlouhy SR, et al. Nat Genet. 1992 Apr;1(1):64-7. doi: 10.1038/ng0492-64. Nat Genet. 1992. PMID: 1363809

10

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

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