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Cited by in F6Publishing
For: Long L, Cai X, Shu Y, Lu Z. A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Straussler-Scheinker syndrome with P102L mutation in PRNP gene. Neurosciences (Riyadh). 2017;22:138-142. [PMID: 28416787 DOI: 10.17712/nsj.2017.2.20160522] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Lambert ZJ, Greenlee JJ, Cassmann ED, West Greenlee MH. Differential Accumulation of Misfolded Prion Strains in Natural Hosts of Prion Diseases. Viruses 2021;13:2453. [PMID: 34960722 DOI: 10.3390/v13122453] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
2 Tesar A, Matej R, Kukal J, Johanidesova S, Rektorova I, Vyhnalek M, Keller J, Eliasova I, Parobkova E, Smetakova M, Musova Z, Rusina R. Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome. Ann Neurol 2019;86:643-52. [PMID: 31397917 DOI: 10.1002/ana.25579] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
3 Zhao MM, Feng LS, Hou S, Shen PP, Cui L, Feng JC. Gerstmann-Sträussler-Scheinker disease: A case report. World J Clin Cases 2019; 7(3): 389-395 [PMID: 30746381 DOI: 10.12998/wjcc.v7.i3.389] [Reference Citation Analysis]