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Journal Abstract Search

251 related items for PubMed ID: 22499312

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  • 2. Creutzfeldt-Jakob disease: case report and review of the literature.
    Spero M, Lazibat I.
    Acta Clin Croat; 2010 Jun; 49(2):181-7. PubMed ID: 21086738
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  • 3. [Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case].
    Dervaux A, Vicart S, Lopes F, Le Borgne MH.
    Encephale; 2001 Jun; 27(2):194-7. PubMed ID: 11407273
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  • 8. Creutzfeldt-Jakob disease: report of four cases and review of the literature.
    Atalay FÖ, Tolunay Ş, Özgün G, Bekar A, Zarifoğlu M.
    Turk Patoloji Derg; 2015 Jun; 31(2):148-52. PubMed ID: 24272930
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  • 14. Autopsy-proven Creutzfeldt-Jakob disease in a patient with a negative 14-3-3 assay and nonspecific EEG and MRI.
    Donahue JE, Hanna PA, Hariharan S.
    Neurol Sci; 2004 Feb; 24(6):411-3. PubMed ID: 14767688
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  • 16. Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.
    Begué C, Martinetto H, Schultz M, Rojas E, Romero C, D'Giano C, Sevlever G, Somoza M, Taratuto AL.
    Neuroepidemiology; 2011 Feb; 37(3-4):193-202. PubMed ID: 22067221
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  • 17. A Heidenhain variant of Creutzfeldt-Jakob disease: forensic implication.
    Rizzo M, Bruni A, Barberio C, Magro G, Foncin JF.
    Forensic Sci Int; 2004 Dec 02; 146 Suppl():S51-4. PubMed ID: 15639587
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  • 19. Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 type.
    Meissner B, Westner IM, Kallenberg K, Krasnianski A, Bartl M, Varges D, Bösenberg C, Kretzschmar HA, Knauth M, Schulz-Schaeffer WJ, Zerr I.
    Neurology; 2005 Nov 22; 65(10):1544-50. PubMed ID: 16221949
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  • 20. An autopsied case of V180I Creutzfeldt-Jakob disease presenting with panencephalopathic-type pathology and a characteristic prion protein type.
    Iwasaki Y, Mori K, Ito M, Nagaoka M, Ieda T, Kitamoto T, Yoshida M, Hashizume Y.
    Neuropathology; 2011 Oct 22; 31(5):540-8. PubMed ID: 21269331
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