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Journal Abstract Search

296 related items for PubMed ID: 1346338

  • 1. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene.
    Medori R, Tritschler HJ, LeBlanc A, Villare F, Manetto V, Chen HY, Xue R, Leal S, Montagna P, Cortelli P.
    N Engl J Med; 1992 Feb 13; 326(7):444-9. PubMed ID: 1346338
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  • 2. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.
    Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, Gray F, Cortelli P, Montagna P, Ghetti B.
    Proc Natl Acad Sci U S A; 1994 Mar 29; 91(7):2839-42. PubMed ID: 7908444
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  • 4. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.
    Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E.
    Brain Pathol; 1995 Jan 29; 5(1):43-51. PubMed ID: 7767490
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  • 5. Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism.
    Medori R, Tritschler HJ.
    Am J Hum Genet; 1993 Oct 29; 53(4):822-7. PubMed ID: 8105681
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  • 6. Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.
    Chapman J, Arlazoroff A, Goldfarb LG, Cervenakova L, Neufeld MY, Werber E, Herbert M, Brown P, Gajdusek DC, Korczyn AD.
    Neurology; 1996 Mar 29; 46(3):758-61. PubMed ID: 8618678
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  • 7. Diffuse thalamic degeneration in fatal familial insomnia. A morphometric study.
    Macchi G, Rossi G, Abbamondi AL, Giaccone G, Mancia D, Tagliavini F, Bugiani O.
    Brain Res; 1997 Oct 10; 771(1):154-8. PubMed ID: 9383019
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  • 8. [Fatal familial insomnia and prion diseases].
    Seilhean D, Duyckaerts C, Hauw JJ.
    Rev Neurol (Paris); 1995 Apr 10; 151(4):225-30. PubMed ID: 7481372
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  • 9. [The spectrum of prion pathology broadens: fatal familial insomnia].
    Delgado-Reyes S, Feito-Ibarz N, Ruiz-Aláez A, García de la Rocha ML, Martín-Araguz A, Moreno-Martínez JM.
    Rev Neurol; 1997 Dec 10; 25(148):2006-14. PubMed ID: 9528048
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  • 10. Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease.
    Taratuto AL, Piccardo P, Reich EG, Chen SG, Sevlever G, Schultz M, Luzzi AA, Rugiero M, Abecasis G, Endelman M, Garcia AM, Capellari S, Xie Z, Lugaresi E, Gambetti P, Dlouhy SR, Ghetti B.
    Neurology; 2002 Feb 12; 58(3):362-7. PubMed ID: 11839833
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  • 11. 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 12; 35(5):1177-88. PubMed ID: 24360565
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  • 14. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.
    Goldfarb LG, Petersen RB, Tabaton M, Brown P, LeBlanc AC, Montagna P, Cortelli P, Julien J, Vital C, Pendelbury WW.
    Science; 1992 Oct 30; 258(5083):806-8. PubMed ID: 1439789
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  • 15. Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report.
    Moody KM, Schonberger LB, Maddox RA, Zou WQ, Cracco L, Cali I.
    BMC Neurol; 2011 Oct 31; 11():136. PubMed ID: 22040318
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  • 16. Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia.
    Gambetti P, Parchi P, Chen SG.
    Clin Lab Med; 2003 Mar 31; 23(1):43-64. PubMed ID: 12733424
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  • 17. Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17.
    Petersen RB, Tabaton M, Chen SG, Monari L, Richardson SL, Lynch T, Manetto V, Lanska DJ, Markesbery WR, Lynches T [corrected to Lynch T].
    Neurology; 1995 Jun 31; 45(6):1062-7. PubMed ID: 7783864
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  • 18. A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease.
    Bosque PJ, Vnencak-Jones CL, Johnson MD, Whitlock JA, McLean MJ.
    Neurology; 1992 Oct 31; 42(10):1864-70. PubMed ID: 1357594
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  • 20. Comparison of the pathologic and pathogenic features in six different regions of postmortem brains of three patients with fatal familial insomnia.
    Xie WL, Shi Q, Xia SL, Zhang BY, Gong HS, Wang SB, Xu Y, Guo Y, Tian C, Zhang J, Xu BL, Liu Y, Dong XP.
    Int J Mol Med; 2013 Jan 31; 31(1):81-90. PubMed ID: 23175354
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