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Journal Abstract Search

204 related items for PubMed ID: 23467330

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  • 3. 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; 8(5):336-8. PubMed ID: 25495585
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  • 7. [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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  • 11. Iatrogenic and sporadic Creutzfeldt-Jakob disease in 2 sisters without mutation in the prion protein gene.
    Frontzek K, Moos R, Schaper E, Jann L, Herfs G, Zimmermann DR, Aguzzi A, Budka H.
    Prion; 2015 Nov 30; 9(6):444-8. PubMed ID: 26634863
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  • 12. [Genetic background of human prion diseases].
    Kovács GG.
    Ideggyogy Sz; 2007 Nov 30; 60(11-12):438-46. PubMed ID: 18198790
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  • 14. [A case of Creutzfeldt-Jakob disease with a double mutation (V180I/M232R) in the PRNP gene].
    Koh K, Takaki R, Miwa M, Nagasaka T, Shindo K, Takiyama Y.
    Rinsho Shinkeigaku; 2015 Nov 30; 55(6):424-7. PubMed ID: 26103817
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  • 16. Novel PRNP mutation in a patient with a slow progressive dementia syndrome.
    Heinemann U, Krasnianski A, Meissner B, Grasbon-Frodl EM, Kretzschmar HA, Zerr I.
    Med Sci Monit; 2008 May 30; 14(5):CS41-43. PubMed ID: 18443555
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  • 17. Reduced cerebral blood flow in genetic prion disease with PRNP D178N-129M mutation: an arterial spin labeling MRI study.
    Chen S, Guan M, Shang JK, He S, Zhang ML, Ma MM, Zhang JW.
    J Clin Neurosci; 2015 Jan 30; 22(1):204-6. PubMed ID: 25220284
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  • 19. Genetic Prion Disease: Insight from the Features and Experience of China National Surveillance for Creutzfeldt-Jakob Disease.
    Shi Q, Chen C, Xiao K, Zhou W, Gao LP, Chen DD, Wu YZ, Wang Y, Hu C, Gao C, Dong XP.
    Neurosci Bull; 2021 Nov 30; 37(11):1570-1582. PubMed ID: 34487324
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