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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

211 related articles for article (PubMed ID: 14966171)

  • 21. Serial magnetic resonance imaging changes in sporadic Creutzfeldt-Jakob disease with valine homozygosity at codon 129 of the prion protein gene.
    Furukawa F; Ishibashi S; Sanjo N; Yamashita H; Mizusawa H
    JAMA Neurol; 2014 Sep; 71(9):1186-7. PubMed ID: 25070174
    [No Abstract]   [Full Text] [Related]  

  • 22. MM2-thalamic-type sporadic Creutzfeldt-Jakob disease with widespread neocortical pathology.
    Hirose K; Iwasaki Y; Izumi M; Yoshida M; Hashizume Y; Kitamoto T; Sahashi K
    Acta Neuropathol; 2006 Oct; 112(4):503-11. PubMed ID: 16957926
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.
    Galeno R; Di Bari MA; Nonno R; Cardone F; Sbriccoli M; Graziano S; Ingrosso L; Fiorini M; Valanzano A; Pasini G; Poleggi A; Vinci R; Ladogana A; Puopolo M; Monaco S; Agrimi U; Zanusso G; Pocchiari M
    J Virol; 2017 Jun; 91(11):. PubMed ID: 28298604
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation.
    Watts JC; Giles K; Serban A; Patel S; Oehler A; Bhardwaj S; Guan S; Greicius MD; Miller BL; DeArmond SJ; Geschwind MD; Prusiner SB
    Ann Neurol; 2015 Oct; 78(4):540-53. PubMed ID: 26094969
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.
    Mitrová E; Belay G
    Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Prion disease].
    Mizusawa H
    Rinsho Shinkeigaku; 2010 Nov; 50(11):797-802. PubMed ID: 21921445
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.
    Parchi P; Cescatti M; Notari S; Schulz-Schaeffer WJ; Capellari S; Giese A; Zou WQ; Kretzschmar H; Ghetti B; Brown P
    Brain; 2010 Oct; 133(10):3030-42. PubMed ID: 20823086
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties.
    Bishop MT; Will RG; Manson JC
    Proc Natl Acad Sci U S A; 2010 Jun; 107(26):12005-10. PubMed ID: 20547859
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinicopathologic characteristics of sporadic Japanese Creutzfeldt-Jakob disease classified according to prion protein gene polymorphism and prion protein type.
    Iwasaki Y; Yoshida M; Hashizume Y; Kitamoto T; Sobue G
    Acta Neuropathol; 2006 Nov; 112(5):561-71. PubMed ID: 16847689
    [TBL] [Abstract][Full Text] [Related]  

  • 31. MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strain.
    Moda F; Suardi S; Di Fede G; Indaco A; Limido L; Vimercati C; Ruggerone M; Campagnani I; Langeveld J; Terruzzi A; Brambilla A; Zerbi P; Fociani P; Bishop MT; Will RG; Manson JC; Giaccone G; Tagliavini F
    Brain Pathol; 2012 Sep; 22(5):662-9. PubMed ID: 22288561
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic Creutzfeldt-Jakob disease-M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case.
    Shintaku M; Nakamura T; Kaneda D; Shinde A; Kusaka H; Takeuchi A; Kitamoto T
    Neuropathology; 2021 Jun; 41(3):206-213. PubMed ID: 33586250
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 28(3):326-32. PubMed ID: 18248577
    [TBL] [Abstract][Full Text] [Related]  

  • 34. An autopsied case of Creutzfeldt-Jakob disease with mutation in the prion protein gene codon 232 and type 1+2 prion protein.
    Iwasaki Y; Yokoi F; Tatsumi S; Mimuro M; Iwai K; Kitamoto T; Yoshida M
    Neuropathology; 2013 Oct; 33(5):568-75. PubMed ID: 23320809
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Co-existence of PrP
    Cali I; Puoti G; Smucny J; Curtiss PM; Cracco L; Kitamoto T; Occhipinti R; Cohen ML; Appleby BS; Gambetti P
    Sci Rep; 2020 Jan; 10(1):1503. PubMed ID: 32001774
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease.
    Schulz-Schaeffer WJ; Giese A; Windl O; Kretzschmar HA
    Clin Neuropathol; 1996; 15(6):353-7. PubMed ID: 8937783
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings.
    Baiardi S; Capellari S; Ladogana A; Strumia S; Santangelo M; Pocchiari M; Parchi P
    J Alzheimers Dis; 2016; 50(2):465-76. PubMed ID: 26682685
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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; 37(5):500-12. PubMed ID: 21450052
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel phenotype of sporadic Creutzfeldt-Jakob disease.
    Giaccone G; Di Fede G; Mangieri M; Limido L; Capobianco R; Suardi S; Grisoli M; Binelli S; Fociani P; Bugiani O; Tagliavini F
    J Neurol Neurosurg Psychiatry; 2007 Dec; 78(12):1379-82. PubMed ID: 18024694
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.