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For: Reñé R, Campdelacreu J, Ferrer I, Escrig A, Povedano M, Gascón-Bayarri J, Moral E. Familial Creutzfeldt-Jakob disease with E200K mutation presenting with neurosensorial hypoacusis. J Neurol Neurosurg Psychiatry 2007;78:103-4. [PMID: 17172576 DOI: 10.1136/jnnp.2006.095588] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]
Number Citing Articles
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2 Baiardi S, Capellari S, Bartoletti Stella A, Parchi P. Unusual Clinical Presentations Challenging the Early Clinical Diagnosis of Creutzfeldt-Jakob Disease. J Alzheimers Dis 2018;64:1051-65. [PMID: 30010123 DOI: 10.3233/JAD-180123] [Cited by in Crossref: 17] [Cited by in F6Publishing: 8] [Article Influence: 5.7] [Reference Citation Analysis]
3 Cohen OS, Kimiagar I, Korczyn AD, Nitsan Z, Appel S, Hoffmann C, Rosenmann H, Kahana E, Chapman J. Unusual presentations in patients with E200K familial Creutzfeldt-Jakob disease. Eur J Neurol 2016;23:871-7. [PMID: 26806765 DOI: 10.1111/ene.12955] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 1.7] [Reference Citation Analysis]
4 Fulbright RK, Hoffmann C, Lee H, Pozamantir A, Chapman J, Prohovnik I. MR imaging of familial Creutzfeldt-Jakob disease: a blinded and controlled study. AJNR Am J Neuroradiol 2008;29:1638-43. [PMID: 18635614 DOI: 10.3174/ajnr.A1217] [Cited by in Crossref: 47] [Cited by in F6Publishing: 34] [Article Influence: 3.4] [Reference Citation Analysis]