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Journal Abstract Search

390 related items for PubMed ID: 23289175

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  • 4. Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2.
    Samman I, Schulz-Schaeffer WJ, Wöhrle JC, Sommer A, Kretzschmar HA, Hennerici M.
    J Neurol Neurosurg Psychiatry; 1999 Nov; 67(5):678-81. PubMed ID: 10519881
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  • 6. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease.
    Collins SJ, Sanchez-Juan P, Masters CL, Klug GM, van Duijn C, Poleggi A, Pocchiari M, Almonti S, Cuadrado-Corrales N, de Pedro-Cuesta J, Budka H, Gelpi E, Glatzel M, Tolnay M, Hewer E, Zerr I, Heinemann U, Kretszchmar HA, Jansen GH, Olsen E, Mitrova E, Alpérovitch A, Brandel JP, Mackenzie J, Murray K, Will RG.
    Brain; 2006 Sep; 129(Pt 9):2278-87. PubMed ID: 16816392
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  • 9. Early-onset spastic paraparesis as presenting sign of familial Creutzfeldt-Jakob disease.
    Conte F, Giordano A, Tortora F, Caiazzo G, Ladogana A, Tedeschi G, Tessitore A.
    Parkinsonism Relat Disord; 2015 Dec; 21(12):1479-80. PubMed ID: 26578040
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  • 10. Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease.
    Hamaguchi T, Kitamoto T, Sato T, Mizusawa H, Nakamura Y, Noguchi M, Furukawa Y, Ishida C, Kuji I, Mitani K, Murayama S, Kohriyama T, Katayama S, Yamashita M, Yamamoto T, Udaka F, Kawakami A, Ihara Y, Nishinaka T, Kuroda S, Suzuki N, Shiga Y, Arai H, Maruyama M, Yamada M.
    Neurology; 2005 Feb 22; 64(4):643-8. PubMed ID: 15728285
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  • 11. Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.
    Shi Q, Shen XJ, Zhou W, Xiao K, Zhang XM, Zhang BY, Dong XP.
    Prion; 2014 Feb 22; 8(6):411-4. PubMed ID: 25482600
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  • 13. Creutzfeldt-Jakob disease: updated diagnostic criteria, treatment algorithm, and the utility of brain biopsy.
    Manix M, Kalakoti P, Henry M, Thakur J, Menger R, Guthikonda B, Nanda A.
    Neurosurg Focus; 2015 Nov 22; 39(5):E2. PubMed ID: 26646926
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  • 14. Familial Creutzfeldt-Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD.
    Cohen OS, Chapman J, Korczyn AD, Nitsan Z, Appel S, Hoffmann C, Rosenmann H, Kahana E, Lee H.
    J Neurol; 2015 Mar 22; 262(3):604-13. PubMed ID: 25522698
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  • 15. Novel prion protein gene mutation at codon 196 (E196A) in a septuagenarian with Creutzfeldt-Jakob disease.
    Zhang H, Wang M, Wu L, Zhang H, Jin T, Wu J, Sun L.
    J Clin Neurosci; 2014 Jan 22; 21(1):175-8. PubMed ID: 23787189
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  • 18. 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 22; 63(6):876-80. PubMed ID: 16769870
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  • 20. Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
    Kretzschmar HA, Ironside JW, DeArmond SJ, Tateishi J.
    Arch Neurol; 1996 Sep 22; 53(9):913-20. PubMed ID: 8815857
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