[1] Fadili H, Tazi R, El Oury H, El Aidaoui K, Hazim A. Report of a case of Creutzfeldt-Jakob disease with an unusual quick evolution[J]. Cureus, 2022, 14:e22982. [2] Bakal JA, Charlton CL, Hlavay B, Jansen GH, Svenson LW, Power C. Progressive multifocal leukoencephalopathy and Creutzfeldt-Jakob disease:population-wide incidences, comorbidities, costs of care, and outcomes[J]. J Neurovirol, 2021, 27:476-481. [3] Bittar J, Joshi P, Genova J, Yeboah K, Kafaie J. Creutzfeldt-Jakob disease presenting as posterior reversible encephalopathy syndrome[J]. Cureus, 2020, 12:e7211. [4] Yang J, Kuang H, Wang Q, Liu J, Chen X, Shang H. Analysis of Chinese patients with sporadic Creutzfeldt-Jakob disease[J]. Prion, 2020, 14:137-142. [5] Bizzi A, Peoc'h K. Amended diagnostic protocol increases the early diagnosis of sporadic Creutzfeldt-Jakob disease[J]. Neurology, 2018, 91:155-156. [6] Salehi P, Clark M, Pinzon J, Patil A. Sporadic Creutzfeldt-Jakob disease[J]. Am J Emerg Med, 2022, 52:267.e1-e3. [7] Katsikaki G, Dagklis IE, Angelopoulos P, Ntantos D, Prevezianou A, Bostantjopoulou S. Atypical and early symptoms of sporadic Creutzfeldt-Jakob disease:case series and review of the literature[J]. Int J Neurosci, 2021, 131:927-938. [8] Baiardi S, Redaelli V, Ripellino P, Rossi M, Franceschini A, Moggio M, Sola P, Ladogana A, Fociani P, Magherini A, Capellari S, Giese A, Caughey B, Caroppo P, Parchi P. Prion-related peripheral neuropathy in sporadic Creutzfeldt-Jakob disease[J]. J Neurol Neurosurg Psychiatry, 2019, 90:424-427. [9] Lahiri D, Pattnaik S, Bhat A, Dubey S, Biswas A, Roy BK. Young-onset sporadic Creutzfeldt-Jakob disease with atypical phenotypic features:a case report[J]. J Med Case Rep, 2019, 13:163. [10] Geschwind MD. Prion diseases[J]. Continuum (Minneap Minn), 2015, 21(6 Neuroinfectious Disease):1612-1638. [11] Appel S, Cohen OS, Chapman J, Gilat S, Rosenmann H, Nitsan Z, Kahan E, Blatt I. The association of quantitative EEG and MRI in Creutzfeldt-Jakob disease[J]. Acta Neurol Scand, 2019, 140:366-371. [12] Appel S, Cohen OS, Chapman J, Gilat S, Rosenmann H, Nitsan Z, Kahana E, Blatt I. Spatial distribution of abnormal EEG activity in Creutzfeldt-Jakob disease[J]. Neurophysiol Clin, 2021, 51:219-224. [13] Kharel H, Adhikari P, Pokhrel NB, Kharel Z, Nepal G. The first reported case of Creutzfeldt-Jakob disease from Nepal[J]. Clin Case Rep, 2019, 8:198-202. [14] Bucelli RC, Ances BM. Diagnosis and evaluation of a patient with rapidly progressive dementia[J]. Mo Med, 2013, 110:422-428. [15] Lu AJ, Hu HQ. Update and changes in diagnostic criteria for paraneoplastic syndrome of the nervous system[J]. Zhongguo Shen Jing Mian Yi Xue He Shen Jing Bing Xue Za Zhi, 2022, 29:501-505.[路爱军, 胡怀强. 神经系统副肿瘤综合征诊断标准的更新与变化[J]. 中国神经免疫学和神经病学杂志, 2022, 29:501-505.] [16] Graus F, Vogrig A, Muñiz-Castrillo S, Antoine JG, Desestret V, Dubey D, Giometto B, Irani SR, Joubert B, Leypoldt F, McKeon A, Prüss H, Psimaras D, Thomas L, Titulaer MJ, Vedeler CA, Verschuuren JJ, Dalmau J, Honnorat J. Updated diagnostic criteria for paraneoplastic neurologic syndromes[J]. Neurol Neuroimmunol Neuroinflamm, 2021, 8:e1014. [17] Blaes F. Pathogenesis, diagnosis and treatment of paraneoplastic neurologic syndromes[J]. Expert Rev Neurother, 2021, 21:675-686. [18] Flanagan EP. Paraneoplastic disorders of the nervous system[J]. Continuum (Minneap Minn), 2020, 26:1602-1628. [19] Cheng G, Zhang J. Imaging features (CT, MRI, MRS, and PET/CT) of primary central nervous system lymphoma in immunocompetent patients[J]. Neurol Sci, 2019, 40:535-542. [20] Zoccarato M, Gastaldi M, Zuliani L, Biagioli T, Brogi M, Bernardi G, Corsini E, Bazzigaluppi E, Fazio R, Giannotta C, Nobile-Orazio E, Costa G, Iorio R, Evoli A, Mariotto S, Ferrari S, Galloni E, De Riva V, Zardini E, Franciotta D, Giometto B. Diagnostics of paraneoplastic neurological syndromes[J]. Neurol Sci, 2017, 38(Suppl 2):237-242. |