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

146 related items for PubMed ID: 20005032

  • 1. Rare E196K mutation in the PRNP gene of a patient exhibiting behavioral abnormalities.
    Béjot Y, Osseby GV, Caillier M, Moreau T, Laplanche JL, Giroud M.
    Clin Neurol Neurosurg; 2010 Apr; 112(3):244-7. PubMed ID: 20005032
    [Abstract] [Full Text] [Related]

  • 2. Novel prion protein gene mutation at codon 196 (E196A) in a septuagenarian with Creutzfeldt-Jakob disease.
    Zhang H, Wang M, Wu L, Zhang H, Jin T, Wu J, Sun L.
    J Clin Neurosci; 2014 Jan; 21(1):175-8. PubMed ID: 23787189
    [Abstract] [Full Text] [Related]

  • 3. Novel prion protein gene mutation in an octogenarian with Creutzfeldt-Jakob disease.
    Collins S, Boyd A, Fletcher A, Byron K, Harper C, McLean CA, Masters CL.
    Arch Neurol; 2000 Jul; 57(7):1058-63. PubMed ID: 10891990
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 9. 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 Jul; 8(5):336-8. PubMed ID: 25495585
    [Abstract] [Full Text] [Related]

  • 10. 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; 14(5):CS41-43. PubMed ID: 18443555
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

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

  • 13. The first Chinese case of Creutzfeldt-Jakob disease patient with R208H mutation in PRNP.
    Chen C, Shi Q, Tian C, Li Q, Zhou W, Gao C, Han J, Dong XP.
    Prion; 2011 Oct; 5(3):232-4. PubMed ID: 21791975
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution.
    Shiga Y, Satoh K, Kitamoto T, Kanno S, Nakashima I, Sato S, Fujihara K, Takata H, Nobukuni K, Kuroda S, Takano H, Umeda Y, Konno H, Nagasato K, Satoh A, Matsuda Y, Hidaka M, Takahashi H, Sano Y, Kim K, Konishi T, Doh-ura K, Sato T, Sasaki K, Nakamura Y, Yamada M, Mizusawa H, Itoyama Y.
    J Neurol; 2007 Nov; 254(11):1509-17. PubMed ID: 17965961
    [Abstract] [Full Text] [Related]

  • 19. Long-duration sCJD with PRNP codon 129 methionine homozygosity and cerebral cortical plaques.
    Lo RY, Shyu WC, Li H.
    Neurology; 2006 Jun 27; 66(12):1944-5. PubMed ID: 16707728
    [Abstract] [Full Text] [Related]

  • 20. Atypical presentation of Creutzfeldt-Jakob disease: the first Italian case associated with E196K mutation in the PRNP gene.
    Clerici F, Elia A, Girotti F, Contri P, Mariani C, Tagliavini F, Di Fede G.
    J Neurol Sci; 2008 Dec 15; 275(1-2):145-7. PubMed ID: 18706660
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.