Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Report
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Failure to ameliorate Creutzfeldt-Jakob disease with amphotericin B therapyMasullo, C ; Macchi, G ; Xi, Y G ; Pocchiari, MThe Journal of infectious diseases, 1992, Vol.165 (4), p.784-785Texto completo disponível |
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Material Type: Report
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A Rare Case of Creutzfeldt-Jakob Disease With Alcohol Use Disorder and Review of LiteratureJoseph, Abraham ; Mushtaq, Hisham ; Zakhia, George ; Rohde, Jonathan ; Whiting, Adria ; Jama, Abbas B ; Khedr, Anwar ; Jain, Nitesh K ; Khan, Syed AnjumCureus, 2022, Vol.14 (5), p.e24812-e24812Texto completo disponível |
3 |
Material Type: Report
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The first reported case of Creutzfeldt-Jakob disease from NepalKharel, Himal ; Adhikari, Pabitra ; Pokhrel, Nishan B ; Kharel, Zeni ; Nepal, GauravClinical case reports, 2020, Vol.8 (1), p.198-202Texto completo disponível |
4 |
Material Type: Report
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Creutzfeldt-Jakob Disease Presenting with Abducens Nerve PalsyAnthony, Christopher M ; Giles, Gregory B ; Justin, Grant A ; Wedel, Marissa L ; Grant, Aaron DCureus, 2019, Vol.11 (9), p.e5564-e5564Texto completo disponível |
5 |
Material Type: Report
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Creutzfeldt-Jakob Disease Presenting as Expressive Aphasia and Nonconvulsive Status EpilepticusMahboob, Hafiz B ; Kaokaf, Kazi H ; Gonda, Jeremy MCase reports in critical care, 2018, Vol.2018, p.5053175-5053175Texto completo disponível |
6 |
Material Type: Report
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A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptomNagata, Tomoyuki ; Shinagawa, Shunichiro ; Kobayashi, Nobuyuki ; Kondo, Kazuhiro ; Shigeta, MasahiroPrion, 2022, Vol.16 (1), p.7-13Taylor & FrancisTexto completo disponível |
7 |
Material Type: Report
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Atypical and early symptoms of sporadic Creutzfeldt - Jakob disease: case series and review of the literatureKatsikaki, Grammatiki ; Dagklis, Ioannis E. ; Angelopoulos, Petros ; Ntantos, Dimitrios ; Prevezianou, Angeliki ; Bostantjopoulou, SevastiInternational Journal of Neuroscience, 2021, Vol.131 (9), p.927-938Taylor & FrancisTexto completo disponível |
8 |
Material Type: Report
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Creutzfeldt-Jakob disease associated with a T188K homozygous mutation in the prion protein gene: a case report and review of the literatureShan, Yuheng ; Zhang, Jiatang ; Cen, Yuying ; Xu, Xiaojiao ; Tan, Ruishu ; Zhao, Jiahua ; Yu, ShengyuanPrion, 2022, Vol.16 (1), p.14-18Taylor & FrancisTexto completo disponível |
9 |
Material Type: Report
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Long-term preservation of pharyngeal swallowing function in MM2-cortical-type sporadic Creutzfeldt-Jakob diseaseHayashi, Yuichi ; Kunieda, Kenjiro ; Kudo, Takuya ; Kimura, Akio ; Fujishima, Ichiro ; Shimohata, TakayoshiPrion, 2021, Vol.15 (1), p.82-86Taylor & FrancisTexto completo disponível |
10 |
Material Type: Report
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Visual hallucinations: an unusual manifestation of sporadic Creutzfeldt-Jakob disease termed the 'Heidenhain variant'Gooriah, R ; Dafalla, B E A ; Tun, S ; Venugopalan, T C ; Lwin, K KJournal of neurology, 2014, Vol.261 (11), p.2228-2229Texto completo disponível |