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Journal Abstract Search

261 related items for PubMed ID: 10932276

  • 1. Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene.
    Rossi G, Giaccone G, Giampaolo L, Iussich S, Puoti G, Frigo M, Cavaletti G, Frattola L, Bugiani O, Tagliavini F.
    Neurology; 2000 Aug 08; 55(3):405-10. PubMed ID: 10932276
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  • 2. Rapidly progressive dementia syndrome associated with a novel four extra repeat mutation in the prion protein gene.
    Yanagihara C, Yasuda M, Maeda K, Miyoshi K, Nishimura Y.
    J Neurol Neurosurg Psychiatry; 2002 Jun 08; 72(6):788-91. PubMed ID: 12023426
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  • 3. Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene.
    Pietrini V, Puoti G, Limido L, Rossi G, Di Fede G, Giaccone G, Mangieri M, Tedeschi F, Bondavalli A, Mancia D, Bugiani O, Tagliavini F.
    Neurology; 2003 Nov 11; 61(9):1288-91. PubMed ID: 14610142
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  • 4. A patient with Creutzfeldt-Jakob disease with an insertion of 7 octa-repeats in the PRNP gene: molecular characteristics and clinical features.
    Guo YJ, Wang XF, Han J, Zhang BY, Zhao WQ, Shi Q, Wan YZ, Gao C, Li JM, Wang DX, Dong XP.
    Am J Med Sci; 2008 Dec 11; 336(6):519-23. PubMed ID: 19092329
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  • 6. Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
    Marcon G, Indaco A, Di Fede G, Suardi S, Finato N, Moretti V, Micoli S, Fociani P, Zerbi P, Pincherle A, Redaelli V, Tagliavini F, Giaccone G.
    Brain Pathol; 2014 Mar 11; 24(2):148-51. PubMed ID: 24118545
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  • 8. [Molecular genetics in Creutzfeldt-Jakob disease].
    Kitamoto T.
    Rinsho Shinkeigaku; 1994 Dec 11; 34(12):1222-3. PubMed ID: 7774117
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  • 11. 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 Dec 11; 8(5):336-8. PubMed ID: 25495585
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  • 14. A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob disease.
    Furukawa H, Doh-ura K, Kikuchi H, Tateishi J, Iwaki T.
    J Neurol Sci; 1998 Jun 11; 158(1):71-5. PubMed ID: 9667781
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  • 17. Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology.
    Jansen C, van Swieten JC, Capellari S, Strammiello R, Parchi P, Rozemuller AJ.
    J Neurol Neurosurg Psychiatry; 2009 Dec 11; 80(12):1386-9. PubMed ID: 19917818
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  • 20. Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.
    Gelpi E, Kovacs GG, Ströbel T, Koperek O, Voigtländer T, Liberski PP, Budka H.
    Acta Neuropathol; 2005 Nov 11; 110(5):513-9. PubMed ID: 16155763
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