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Journal Abstract Search

420 related items for PubMed ID: 12733424

  • 1. Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia.
    Gambetti P, Parchi P, Chen SG.
    Clin Lab Med; 2003 Mar; 23(1):43-64. PubMed ID: 12733424
    [Abstract] [Full Text] [Related]

  • 2. Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
    Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, Ruf V, Windl O, Capellari S, Parchi P.
    Acta Neuropathol; 2021 Oct; 142(4):707-728. PubMed ID: 34324063
    [Abstract] [Full Text] [Related]

  • 3. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
    Schmitz M, Lüllmann K, Zafar S, Ebert E, Wohlhage M, Oikonomou P, Schlomm M, Mitrova E, Beekes M, Zerr I.
    Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565
    [Abstract] [Full Text] [Related]

  • 4. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.
    Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E.
    Brain Pathol; 1995 Jan; 5(1):43-51. PubMed ID: 7767490
    [Abstract] [Full Text] [Related]

  • 5. Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.
    Pastore M, Chin SS, Bell KL, Dong Z, Yang Q, Yang L, Yuan J, Chen SG, Gambetti P, Zou WQ.
    Am J Pathol; 2005 Dec; 167(6):1729-38. PubMed ID: 16314483
    [Abstract] [Full Text] [Related]

  • 6. Virus Infection, Genetic Mutations, and Prion Infection in Prion Protein Conversion.
    Hara H, Sakaguchi S.
    Int J Mol Sci; 2021 Nov 18; 22(22):. PubMed ID: 34830321
    [Abstract] [Full Text] [Related]

  • 7. Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures.
    Cassard H, Huor A, Espinosa JC, Douet JY, Lugan S, Aron N, Vilette D, Delisle MB, Marín-Moreno A, Peran P, Beringue V, Torres JM, Ironside JW, Andreoletti O.
    mBio; 2020 Jun 16; 11(3):. PubMed ID: 32546613
    [Abstract] [Full Text] [Related]

  • 8. Clinical features of sporadic fatal insomnia.
    Barash JA.
    Rev Neurol Dis; 2009 Jun 16; 6(3):E87-93. PubMed ID: 19898273
    [Abstract] [Full Text] [Related]

  • 9. Transgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease.
    Bouybayoune I, Mantovani S, Del Gallo F, Bertani I, Restelli E, Comerio L, Tapella L, Baracchi F, Fernández-Borges N, Mangieri M, Bisighini C, Beznoussenko GV, Paladini A, Balducci C, Micotti E, Forloni G, Castilla J, Fiordaliso F, Tagliavini F, Imeri L, Chiesa R.
    PLoS Pathog; 2015 Apr 16; 11(4):e1004796. PubMed ID: 25880443
    [Abstract] [Full Text] [Related]

  • 10. Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis.
    Capellari S, Strammiello R, Saverioni D, Kretzschmar H, Parchi P.
    Acta Neuropathol; 2011 Jan 16; 121(1):21-37. PubMed ID: 20978903
    [Abstract] [Full Text] [Related]

  • 11. Towards authentic transgenic mouse models of heritable PrP prion diseases.
    Watts JC, Giles K, Bourkas ME, Patel S, Oehler A, Gavidia M, Bhardwaj S, Lee J, Prusiner SB.
    Acta Neuropathol; 2016 Oct 16; 132(4):593-610. PubMed ID: 27350609
    [Abstract] [Full Text] [Related]

  • 12. Transgenic mice recapitulate the phenotypic heterogeneity of genetic prion diseases without developing prion infectivity: Role of intracellular PrP retention in neurotoxicity.
    Chiesa R, Restelli E, Comerio L, Del Gallo F, Imeri L.
    Prion; 2016 Mar 03; 10(2):93-102. PubMed ID: 26864450
    [Abstract] [Full Text] [Related]

  • 13. Comparison of the pathologic and pathogenic features in six different regions of postmortem brains of three patients with fatal familial insomnia.
    Xie WL, Shi Q, Xia SL, Zhang BY, Gong HS, Wang SB, Xu Y, Guo Y, Tian C, Zhang J, Xu BL, Liu Y, Dong XP.
    Int J Mol Med; 2013 Jan 03; 31(1):81-90. PubMed ID: 23175354
    [Abstract] [Full Text] [Related]

  • 14. Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene.
    Di Fede G, Catania M, Atzori C, Moda F, Pasquali C, Indaco A, Grisoli M, Zuffi M, Guaita MC, Testi R, Taraglio S, Sessa M, Gusmaroli G, Spinelli M, Salzano G, Legname G, Tarletti R, Godi L, Pocchiari M, Tagliavini F, Imperiale D, Giaccone G.
    Acta Neuropathol Commun; 2019 Jan 03; 7(1):1. PubMed ID: 30606247
    [Abstract] [Full Text] [Related]

  • 15. An overview of human prion diseases.
    Imran M, Mahmood S.
    Virol J; 2011 Dec 24; 8():559. PubMed ID: 22196171
    [Abstract] [Full Text] [Related]

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  • 17. The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients.
    Moore RA, Head MW, Ironside JW, Ritchie DL, Zanusso G, Choi YP, Priola SA.
    PLoS Pathog; 2016 Feb 24; 12(2):e1005416. PubMed ID: 26840342
    [Abstract] [Full Text] [Related]

  • 18. Allelic origin of the abnormal prion protein isoform in familial prion diseases.
    Chen SG, Parchi P, Brown P, Capellari S, Zou W, Cochran EJ, Vnencak-Jones CL, Julien J, Vital C, Mikol J, Lugaresi E, Autilio-Gambetti L, Gambetti P.
    Nat Med; 1997 Sep 24; 3(9):1009-15. PubMed ID: 9288728
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