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For: Jankovska N, Rusina R, Bruzova M, Parobkova E, Olejar T, Matej R. Human Prion Disorders: Review of the Current Literature and a Twenty-Year Experience of the National Surveillance Center in the Czech Republic. Diagnostics (Basel) 2021;11:1821. [PMID: 34679519 DOI: 10.3390/diagnostics11101821] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Nakaie M, Katayama F, Nakagaki T, Yoshida S, Kawasaki M, Nishi K, Ogawa K, Toriba A, Nishida N, Nakayama M, Fuchigami T. Synthesis and Biological Evaluation of Novel 2-(Benzofuran-2-yl)-chromone Derivatives for In Vivo Imaging of Prion Deposits in the Brain. ACS Infect Dis 2022;8:1869-82. [PMID: 35969484 DOI: 10.1021/acsinfecdis.2c00142] [Reference Citation Analysis]
2 Antonioni A, Raho EM, Gozzi A, Cotta Ramusino N, Cesnik E, Padroni M, De Vito A, Pugliatti M, Tugnoli V. Case Report: A Case of Creutzfeldt–Jakob Heidenhain Variant Simulating PRES. Diagnostics 2022;12:1558. [DOI: 10.3390/diagnostics12071558] [Reference Citation Analysis]
3 Jankovska N, Rusina R, Keller J, Kukal J, Bruzova M, Parobkova E, Olejar T, Matej R. Biomarkers Analysis and Clinical Manifestations in Comorbid Creutzfeldt–Jakob Disease: A Retrospective Study in 215 Autopsy Cases. Biomedicines 2022;10:680. [DOI: 10.3390/biomedicines10030680] [Reference Citation Analysis]
4 Jankovska N, Matej R, Olejar T. Extracellular Prion Protein Aggregates in Nine Gerstmann–Sträussler–Scheinker Syndrome Subjects with Mutation P102L: A Micromorphological Study and Comparison with Literature Data. IJMS 2021;22:13303. [DOI: 10.3390/ijms222413303] [Reference Citation Analysis]