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5. Clinical features and diagnosis of the MM2 cortical subtype of sporadic Creutzfeldt-Jakob disease. Krasnianski A; Meissner B; Schulz-Schaeffer W; Kallenberg K; Bartl M; Heinemann U; Varges D; Kretzschmar HA; Zerr I Arch Neurol; 2006 Jun; 63(6):876-80. PubMed ID: 16769870 [TBL] [Abstract][Full Text] [Related]
6. An unusually presenting case of sCJD--the VV1 subtype. Tanev KS; Yilma M Clin Neurol Neurosurg; 2009 Apr; 111(3):282-91. PubMed ID: 18995952 [TBL] [Abstract][Full Text] [Related]
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8. Clinical course in young patients with sporadic Creutzfeldt-Jakob disease. Boesenberg C; Schulz-Schaeffer WJ; Meissner B; Kallenberg K; Bartl M; Heinemann U; Krasnianski A; Stoeck K; Varges D; Windl O; Kretzschmar HA; Zerr I Ann Neurol; 2005 Oct; 58(4):533-43. PubMed ID: 16037975 [TBL] [Abstract][Full Text] [Related]
9. MM2-cortical-type sporadic Creutzfeldt-Jakob disease with early stage cerebral cortical pathology presenting with a rapidly progressive clinical course. Niimi Y; Iwasaki Y; Umemura T; Tanaka F; Yoshida M; Hashizume Y; Kitamoto T; Hirayama M; Sobue G Neuropathology; 2008 Dec; 28(6):645-51. PubMed ID: 18410280 [TBL] [Abstract][Full Text] [Related]
10. [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; 27(2):194-7. PubMed ID: 11407273 [TBL] [Abstract][Full Text] [Related]
11. MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology. Hoshino A; Iwasaki Y; Izumi M; Kimura S; Ibi T; Kitamoto T; Yoshida M; Hashizume Y; Sahashi K Neuropathology; 2008 Jun; 28(3):326-32. PubMed ID: 18248577 [TBL] [Abstract][Full Text] [Related]
12. MRI in the diagnosis of sporadic Creutzfeldt-Jakob disease: a study on inter-observer agreement. Tschampa HJ; Kallenberg K; Urbach H; Meissner B; Nicolay C; Kretzschmar HA; Knauth M; Zerr I Brain; 2005 Sep; 128(Pt 9):2026-33. PubMed ID: 15958503 [TBL] [Abstract][Full Text] [Related]
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15. Magnetic resonance spectroscopy and measurement of tau epitopes of autopsy proven sporadic Creutzfeldt-Jakob disease in a patient with non-specific initial EEG, MRI and negative 14-3-3 immunoblot. Sarac H; Hajnsek S; Basić S; Henigsberg N; Rados M; Simić G Coll Antropol; 2008 Jan; 32 Suppl 1():199-204. PubMed ID: 18405083 [TBL] [Abstract][Full Text] [Related]
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17. Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles. Lewis V; Hill AF; Klug GM; Boyd A; Masters CL; Collins SJ Neurology; 2005 Jul; 65(1):113-8. PubMed ID: 16009895 [TBL] [Abstract][Full Text] [Related]
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20. 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; 37(3-4):193-202. PubMed ID: 22067221 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]