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154 related items for PubMed ID: 21791975

  • 1. 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; 5(3):232-4. PubMed ID: 21791975
    [Abstract] [Full Text] [Related]

  • 2. The first Chinese case of Creutzfeldt-Jakob disease with mutation of E200K in PRNP.
    Gao C, Shi Q, Zhou W, Tian C, Jiang HY, Han BY, Dong XP.
    Biomed Environ Sci; 2010 Apr; 23(2):158-60. PubMed ID: 20514992
    [Abstract] [Full Text] [Related]

  • 3. Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years.
    Rudge P, Jaunmuktane Z, Adlard P, Bjurstrom N, Caine D, Lowe J, Norsworthy P, Hummerich H, Druyeh R, Wadsworth JD, Brandner S, Hyare H, Mead S, Collinge J.
    Brain; 2015 Nov; 138(Pt 11):3386-99. PubMed ID: 26268531
    [Abstract] [Full Text] [Related]

  • 4. A Chinese Creutzfeldt-Jakob disease patient with E196K mutation in PRNP.
    Shi Q, Chen C, Song XN, Gao C, Tian C, Zhou W, Song XH, Yao LS, Han J, Dong XP.
    Prion; 2011 Nov; 5(2):117-20. PubMed ID: 21597335
    [Abstract] [Full Text] [Related]

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

  • 6. Rare V203I mutation in the PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.
    Shi Q, Chen C, Wang XJ, Zhou W, Wang JC, Zhang BY, Gao C, Gao C, Han J, Dong XP.
    Prion; 2013 Nov; 7(3):259-62. PubMed ID: 23764840
    [Abstract] [Full Text] [Related]

  • 7. 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; 24(2):148-51. PubMed ID: 24118545
    [Abstract] [Full Text] [Related]

  • 8. Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.
    Roeber S, Krebs B, Neumann M, Windl O, Zerr I, Grasbon-Frodl EM, Kretzschmar HA.
    Acta Neuropathol; 2005 Apr; 109(4):443-8. PubMed ID: 15739100
    [Abstract] [Full Text] [Related]

  • 9. Rare E196A mutation in PRNP gene of 3 Chinese patients with Creutzfeldt-Jacob disease.
    Shi Q, Zhou W, Chen C, Zhang BY, Xiao K, Wang Y, Dong XP.
    Prion; 2016 Jul 03; 10(4):331-7. PubMed ID: 27310471
    [Abstract] [Full Text] [Related]

  • 10. 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 03; 112(3):244-7. PubMed ID: 20005032
    [Abstract] [Full Text] [Related]

  • 11. 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 03; 21(1):175-8. PubMed ID: 23787189
    [Abstract] [Full Text] [Related]

  • 12. Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.
    Shi Q, Shen XJ, Zhou W, Xiao K, Zhang XM, Zhang BY, Dong XP.
    Prion; 2014 Jan 03; 8(6):411-4. PubMed ID: 25482600
    [Abstract] [Full Text] [Related]

  • 13. Human prion protein (PrP) 219K is converted to PrPSc but shows heterozygous inhibition in variant Creutzfeldt-Jakob disease infection.
    Hizume M, Kobayashi A, Teruya K, Ohashi H, Ironside JW, Mohri S, Kitamoto T.
    J Biol Chem; 2009 Feb 06; 284(6):3603-9. PubMed ID: 19074151
    [Abstract] [Full Text] [Related]

  • 14. Mutations at codons 178, 200-129, and 232 contributed to the inherited prion diseases in Korean patients.
    Choi BY, Kim SY, Seo SY, An SS, Kim S, Park SE, Lee SH, Choi YJ, Kim SJ, Kim CK, Park JS, Ju YR.
    BMC Infect Dis; 2009 Aug 22; 9():132. PubMed ID: 19698114
    [Abstract] [Full Text] [Related]

  • 15. Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease.
    Gabizon R, Rosenman H, Meiner Z, Kahana I, Kahana E, Shugart Y, Ott J, Prusiner SB.
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar 29; 343(1306):385-90. PubMed ID: 7913755
    [Abstract] [Full Text] [Related]

  • 16. Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population.
    Jeong BH, Lee KH, Kim NH, Jin JK, Kim JI, Carp RI, Kim YS.
    Neurogenetics; 2005 Dec 29; 6(4):229-32. PubMed ID: 16217673
    [Abstract] [Full Text] [Related]

  • 17. Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology?
    Kobayashi A, Parchi P, Yamada M, Brown P, Saverioni D, Matsuura Y, Takeuchi A, Mohri S, Kitamoto T.
    J Virol; 2015 Apr 29; 89(7):3939-46. PubMed ID: 25609817
    [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 29; 254(11):1509-17. PubMed ID: 17965961
    [Abstract] [Full Text] [Related]

  • 19. 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 29; 35(5):1177-88. PubMed ID: 24360565
    [Abstract] [Full Text] [Related]

  • 20. Corticobasal manifestations of Creutzfeldt-Jakob disease with D178N-homozygous 129M genotype.
    Huang Y, Jianfang M, Morales R, Tang H.
    Prion; 2020 Dec 29; 14(1):232-237. PubMed ID: 32946318
    [Abstract] [Full Text] [Related]

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