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Journal Abstract Search

207 related items for PubMed ID: 8008177

  • 41. Creutzfeldt-Jakob disease with homozygous M232R mutation: A case report.
    Kon T, Miki Y, Arai A, Funamizu Y, Ueno T, Haga R, Nishijima H, Suzuki C, Nunomura J, Baba M, Oyama Y, Shiga Y, Kitamoto T, Tomiyama M.
    J Neurol Sci; 2015 May 15; 352(1-2):108-9. PubMed ID: 25818675
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  • 42. Leads from the MMWR. Update: Creutzfeldt-Jakob disease in a patient receiving a cadaveric dura mater graft.
    JAMA; 1987 Jul 17; 258(3):309-10. PubMed ID: 3298705
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  • 43. Clinical experiences with Creutzfeldt-Jakob disease: three case studies.
    Szucs A, Várallyay P, Osztie E, Papp E, Sólyom A, Finta L, Varga D, Barcs G, Holló A, Kamondi A.
    Ideggyogy Sz; 2012 Nov 30; 65(11-12):401-10. PubMed ID: 23289175
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  • 45. Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene.
    Komatsu J, Sakai K, Hamaguchi T, Sugiyama Y, Iwasa K, Yamada M.
    Prion; 2014 Nov 30; 8(5):336-8. PubMed ID: 25495585
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  • 48. Probable Creutzfeldt-Jakob disease after a cadaveric dural graft.
    Lang CJ, Schüler P, Engelhardt A, Spring A, Brown P.
    Eur J Epidemiol; 1995 Feb 30; 11(1):79-81. PubMed ID: 7489777
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  • 50. Neurosurgery in a patient with Creutzfeldt-Jakob disease after pituitary derived growth hormone therapy in childhood.
    Holmes SJ, Ironside JW, Shalet SM.
    J Neurol Neurosurg Psychiatry; 1996 Mar 30; 60(3):333-5. PubMed ID: 8609514
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  • 51. Intracerebroventricular delivery of dominant negative prion protein in a mouse model of iatrogenic Creutzfeldt-Jakob disease after dura graft transplantation.
    Furuya K, Kawahara N, Yamakawa Y, Kishida H, Hachiya NS, Nishijima M, Kirino T, Kaneko K.
    Neurosci Lett; 2006 Jul 24; 402(3):222-6. PubMed ID: 16759805
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  • 52. Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.
    Head MW, Bunn TJ, Bishop MT, McLoughlin V, Lowrie S, McKimmie CS, Williams MC, McCardle L, MacKenzie J, Knight R, Will RG, Ironside JW.
    Ann Neurol; 2004 Jun 24; 55(6):851-9. PubMed ID: 15174020
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  • 53. Dura mater is a potential source of Aβ seeds.
    Kovacs GG, Lutz MI, Ricken G, Ströbel T, Höftberger R, Preusser M, Regelsberger G, Hönigschnabl S, Reiner A, Fischer P, Budka H, Hainfellner JA.
    Acta Neuropathol; 2016 Jun 24; 131(6):911-23. PubMed ID: 27016065
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  • 54. 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 24; 31(2):148-52. PubMed ID: 24272930
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  • 58. Insight into the frequent occurrence of dura mater graft-associated Creutzfeldt-Jakob disease in Japan.
    Hamaguchi T, Sakai K, Noguchi-Shinohara M, Nozaki I, Takumi I, Sanjo N, Sadakane A, Nakamura Y, Kitamoto T, Saito N, Mizusawa H, Yamada M.
    J Neurol Neurosurg Psychiatry; 2013 Oct 24; 84(10):1171-5. PubMed ID: 23595947
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  • 59. Creutzfeldt-Jakob disease: a case report and differential diagnoses.
    Kojima G, Tatsuno BK, Inaba M, Velligas S, Masaki K, Liow KK.
    Hawaii J Med Public Health; 2013 Apr 24; 72(4):136-9. PubMed ID: 23795314
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  • 60. [Human prion diseases: the Hungarian experience].
    Kovács GG, Bakos A, Mitrova E, Minárovits J, László L, Majtényi K.
    Ideggyogy Sz; 2007 Nov 30; 60(11-12):447-52. PubMed ID: 18200749
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