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Cited by in F6Publishing
For: Yang J, Kuang H, Wang Q, Liu J, Chen X, Shang H. Analysis of Chinese patients with sporadic Creutzfeldt-Jakob disease. Prion 2020;14:137-42. [PMID: 32378453 DOI: 10.1080/19336896.2020.1761515] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Tejedor-romero L, López-cuadrado T, Almazán-isla J, Calero M, García López FJ, de Pedro-cuesta J. Survival Patterns of Human Prion Diseases in Spain, 1998–2018: Clinical Phenotypes and Etiological Clues. Front Neurosci 2022;15:773727. [DOI: 10.3389/fnins.2021.773727] [Reference Citation Analysis]
2 Feng S, Zhao X, Zhou X, Ye X, Yu X, Jiang W, Deng Y, Zhou S, Ma L, Shan P, Zhou G. Epidemiological and Clinical Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Study in Eastern China. Front Neurol 2021;12:700485. [PMID: 34690910 DOI: 10.3389/fneur.2021.700485] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
3 Čiauškaitė J, Puleikytė I, Jesmanas S, Jurkevičienė G, Vaitkus A, Rastenytė D. Creutzfeldt-Jakob disease with neuroleptic malignant syndrome. Clin Case Rep 2021;9:e04699. [PMID: 34466255 DOI: 10.1002/ccr3.4699] [Cited by in F6Publishing: 1] [Reference Citation Analysis]