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Journal Abstract Search

172 related items for PubMed ID: 7902693

  • 1. A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.
    Pocchiari M, Salvatore M, Cutruzzolá F, Genuardi M, Allocatelli CT, Masullo C, Macchi G, Alemá G, Galgani S, Xi YG.
    Ann Neurol; 1993 Dec; 34(6):802-7. PubMed ID: 7902693
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  • 2. 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
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  • 3. Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease.
    Hsiao K, Meiner Z, Kahana E, Cass C, Kahana I, Avrahami D, Scarlato G, Abramsky O, Prusiner SB, Gabizon R.
    N Engl J Med; 1991 Apr 18; 324(16):1091-7. PubMed ID: 2008182
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  • 4. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.
    Mitrová E, Belay G.
    Acta Virol; 2002 Apr 18; 46(1):31-9. PubMed ID: 12197632
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  • 7. [A case of Creutzfeldt-Jakob disease with a point mutation of prion protein at codon 180].
    Tanaka T, Kinoshita I, Saitoh Y, Satoh K, Nishiura Y, Shirabe S, Kitamoto T.
    No To Shinkei; 2004 Dec 18; 56(12):1025-8. PubMed ID: 15729879
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  • 8. [Creutzfeldt-Jakob disease with a point mutation at codon 232 of prion protein--a case report].
    Shimizu T, Tanaka K, Tanahashi N, Fukuuchi Y, Kitamoto T.
    Rinsho Shinkeigaku; 1994 Jun 18; 34(6):590-2. PubMed ID: 7955719
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  • 10. [A case of probable Creutzfeldt-Jakob disease with a point mutation of prion protein gene codon 180 and atypical MRI findings].
    Kobayashi S, Ohuchi T, Maki T.
    Rinsho Shinkeigaku; 1997 Aug 18; 37(8):671-4. PubMed ID: 9404141
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  • 11. Polymorphism at 3' UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt-Jakob disease.
    Jeong BH, Kim NH, Choi EK, Lee C, Song YH, Kim JI, Carp RI, Kim YS.
    Eur J Hum Genet; 2005 Sep 18; 13(9):1094-7. PubMed ID: 15986038
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  • 13. A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease.
    Ripoll L, Laplanche JL, Salzmann M, Jouvet A, Planques B, Dussaucy M, Chatelain J, Beaudry P, Launay JM.
    Neurology; 1993 Oct 18; 43(10):1934-8. PubMed ID: 8105421
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  • 19. Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disorders.
    Schröder B, Franz B, Hempfling P, Selbert M, Jürgens T, Kretzschmar HA, Bodemer M, Poser S, Zerr I.
    Hum Genet; 2001 Sep 18; 109(3):319-25. PubMed ID: 11702213
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  • 20. [Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles].
    Iwaski Y, Sone M, Kato T, Yoshida E, Indo T, Yoshida M, Hashizume Y, Yamada M.
    Rinsho Shinkeigaku; 1999 Aug 18; 39(8):800-6. PubMed ID: 10586622
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