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Journal Abstract Search

139 related items for PubMed ID: 8575203

  • 1. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: a tale of two diseases with the same genetic mutation.
    Gambetti P.
    Curr Top Microbiol Immunol; 1996; 207():19-25. PubMed ID: 8575203
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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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  • 11. 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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  • 12. Sleep, genes and death: fatal familial insomnia.
    Fiorino AS.
    Brain Res Brain Res Rev; 1996 Oct 13; 22(3):258-64. PubMed ID: 8957563
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  • 13. Quantitative Magnetic Resonance Abnormalities in Creutzfeldt-Jakob Disease and Fatal Insomnia.
    Grau-Rivera O, Calvo A, Bargalló N, Monté GC, Nos C, Lladó A, Molinuevo JL, Gelpi E, Sánchez-Valle R.
    J Alzheimers Dis; 2017 Oct 13; 55(1):431-443. PubMed ID: 27662320
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  • 15. [Fatal familial insomnia: phenotypic changes determined by polymorphism of the codon 129].
    Colombier C, Géraud G, Delisle MB, Laplanche JL, Pavy le Traon A, Alizé P, Delpla PA.
    Rev Neurol (Paris); 1997 May 13; 153(4):239-43. PubMed ID: 9296141
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  • 20. [Familial fatal insomnia: a human prion disease which opens the door to a greater understanding of the thalamus].
    Barriga F, Ruiz-Domínguez JA, Velayos JL.
    Rev Med Univ Navarra; 1997 May 13; 41(4):224-8. PubMed ID: 10420962
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