These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

596 related items for PubMed ID: 16923954

  • 1. Classification of sporadic Creutzfeldt-Jakob disease revisited.
    Cali I, Castellani R, Yuan J, Al-Shekhlee A, Cohen ML, Xiao X, Moleres FJ, Parchi P, Zou WQ, Gambetti P.
    Brain; 2006 Sep; 129(Pt 9):2266-77. PubMed ID: 16923954
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.
    Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, Ghetti B, Gambetti P, Kretzschmar H.
    Ann Neurol; 1999 Aug; 46(2):224-33. PubMed ID: 10443888
    [Abstract] [Full Text] [Related]

  • 4. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics.
    Cali I, Castellani R, Alshekhlee A, Cohen Y, Blevins J, Yuan J, Langeveld JP, Parchi P, Safar JG, Zou WQ, Gambetti P.
    Brain; 2009 Oct; 132(Pt 10):2643-58. PubMed ID: 19734292
    [Abstract] [Full Text] [Related]

  • 5. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.
    Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AA, Trojanowski JQ, Petersen RB, Gambetti P.
    Ann Neurol; 1996 Jun; 39(6):767-78. PubMed ID: 8651649
    [Abstract] [Full Text] [Related]

  • 6. Two-dimensional mapping of three phenotype-associated isoforms of the prion protein in sporadic Creutzfeldt-Jakob disease.
    Zanusso G, Righetti PG, Ferrari S, Terrin L, Farinazzo A, Cardone F, Pocchiari M, Rizzuto N, Monaco S.
    Electrophoresis; 2002 Jan; 23(2):347-55. PubMed ID: 11840543
    [Abstract] [Full Text] [Related]

  • 7. Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles.
    Lewis V, Hill AF, Klug GM, Boyd A, Masters CL, Collins SJ.
    Neurology; 2005 Jul 12; 65(1):113-8. PubMed ID: 16009895
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.
    Parchi P, Capellari S, Gambetti P.
    Microsc Res Tech; 2000 Jul 01; 50(1):16-25. PubMed ID: 10871544
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. MRI lesion profiles in sporadic Creutzfeldt-Jakob disease.
    Meissner B, Kallenberg K, Sanchez-Juan P, Collie D, Summers DM, Almonti S, Collins SJ, Smith P, Cras P, Jansen GH, Brandel JP, Coulthart MB, Roberts H, Van Everbroeck B, Galanaud D, Mellina V, Will RG, Zerr I.
    Neurology; 2009 Jun 09; 72(23):1994-2001. PubMed ID: 19506221
    [Abstract] [Full Text] [Related]

  • 15. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
    Faucheux BA, Morain E, Diouron V, Brandel JP, Salomon D, Sazdovitch V, Privat N, Laplanche JL, Hauw JJ, Haïk S.
    Neuropathol Appl Neurobiol; 2011 Aug 09; 37(5):500-12. PubMed ID: 21450052
    [Abstract] [Full Text] [Related]

  • 16. Different prion conformers target the olfactory pathway in sporadic Creutzfeldt-Jakob disease.
    Zanusso G, Ferrari S, Benedetti D, Sbriccoli M, Rizzuto N, Monaco S.
    Ann N Y Acad Sci; 2009 Jul 09; 1170():637-43. PubMed ID: 19686205
    [Abstract] [Full Text] [Related]

  • 17. MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology.
    Hoshino A, Iwasaki Y, Izumi M, Kimura S, Ibi T, Kitamoto T, Yoshida M, Hashizume Y, Sahashi K.
    Neuropathology; 2008 Jun 09; 28(3):326-32. PubMed ID: 18248577
    [Abstract] [Full Text] [Related]

  • 18. Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease.
    Polymenidou M, Stoeck K, Glatzel M, Vey M, Bellon A, Aguzzi A.
    Lancet Neurol; 2005 Dec 09; 4(12):805-14. PubMed ID: 16297838
    [Abstract] [Full Text] [Related]

  • 19. Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene.
    Capellari S, Cardone F, Notari S, Schininà ME, Maras B, Sità D, Baruzzi A, Pocchiari M, Parchi P.
    Neurology; 2005 Mar 08; 64(5):905-7. PubMed ID: 15753435
    [Abstract] [Full Text] [Related]

  • 20. Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type.
    Pan T, Li R, Kang SC, Pastore M, Wong BS, Ironside J, Gambetti P, Sy MS.
    J Neurochem; 2005 Jan 08; 92(1):132-42. PubMed ID: 15606903
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 30.