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For: Smid J, Studart A Neto, Landemberger MC, Machado CF, Nóbrega PR, Canedo NHS, Schultz RR, Naslavsky MS, Rosemberg S, Kok F, Chimelli L, Martins VR, Nitrini R. High phenotypic variability in Gerstmann-Sträussler-Scheinker disease. Arq Neuropsiquiatr 2017;75:331-8. [PMID: 28658400 DOI: 10.1590/0004-282X20170049] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.4] [Reference Citation Analysis]
Number Citing Articles
1 Ota K, Nakazato Y, Yokoyama R, Kawasaki H, Tamura N, Ohtake A, Saito-Tsuruoka M, Yamamoto T. A Japanese family with P102L Gerstmann-Sträussler-Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report. eNeurologicalSci 2021;25:100380. [PMID: 34841096 DOI: 10.1016/j.ensci.2021.100380] [Reference Citation Analysis]
2 Sousa IP Jr, Dos Santos FB, de Paula VS, Vieira TCRG, Dias HG, Barros CA, da Silva EE. Viral and Prion Infections Associated with Central Nervous System Syndromes in Brazil. Viruses 2021;13:1370. [PMID: 34372576 DOI: 10.3390/v13071370] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
3 Anderson K, Overcast W, Brosch J, Graner B, Veronesi M. Prionopathies and Prionlike Protein Aberrations in Neurodegenerative Diseases. neurograph 2021;11:127-148. [DOI: 10.3174/ng.2000035] [Reference Citation Analysis]
4 Mbizvo GK, Ziso B, Larner AJ. Epilepsy and prion diseases: A narrative review. Epilepsy Behav 2021;115:107630. [PMID: 33309427 DOI: 10.1016/j.yebeh.2020.107630] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
5 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]
6 Ghetti B, Piccardo P, Zanusso G. Dominantly inherited prion protein cerebral amyloidoses - a modern view of Gerstmann-Sträussler-Scheinker. Handb Clin Neurol 2018;153:243-69. [PMID: 29887140 DOI: 10.1016/B978-0-444-63945-5.00014-3] [Cited by in Crossref: 25] [Cited by in F6Publishing: 13] [Article Influence: 6.3] [Reference Citation Analysis]
7 Araújo AQC. Unveiling the mysteries of hereditary prion diseases in Brazil. Arq Neuro-Psiquiatr 2017;75:329-330. [DOI: 10.1590/0004-282x20170057] [Reference Citation Analysis]