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Journal Abstract Search

129 related items for PubMed ID: 9521257

  • 1. Fatal familial insomnia: genetic, neuropathologic, and biochemical study of a patient from a new Italian kindred.
    Rossi G, Macchi G, Porro M, Giaccone G, Bugiani M, Scarpini E, Scarlato G, Molini GE, Sasanelli F, Bugiani O, Tagliavini F.
    Neurology; 1998 Mar; 50(3):688-92. PubMed ID: 9521257
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  • 6. 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(1):81-90. PubMed ID: 23175354
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  • 7. 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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  • 8. 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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  • 9. Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene.
    Sun L, Li X, Lin X, Yan F, Chen K, Xiao S.
    Prion; 2015 Feb 12; 9(3):228-35. PubMed ID: 26074146
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  • 10. Early age of onset in fatal familial insomnia. Two novel cases and review of the literature.
    Harder A, Gregor A, Wirth T, Kreuz F, Schulz-Schaeffer WJ, Windl O, Plotkin M, Amthauer H, Neukirch K, Kretzschmar HA, Kuhlmann T, Braas R, Hahne HH, Jendroska K.
    J Neurol; 2004 Jun 12; 251(6):715-24. PubMed ID: 15311348
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  • 12. Fatal familial insomnia: clinical features and molecular genetics.
    Cortelli P, Gambetti P, Montagna P, Lugaresi E.
    J Sleep Res; 1999 Jun 12; 8 Suppl 1():23-9. PubMed ID: 10389103
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  • 13. Clinical and genetic studies of fatal familial insomnia.
    Reder AT, Mednick AS, Brown P, Spire JP, Van Cauter E, Wollmann RL, Cervenàkovà L, Goldfarb LG, Garay A, Ovsiew F.
    Neurology; 1995 Jun 12; 45(6):1068-75. PubMed ID: 7783865
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  • 14. Does the clinical phenotype of fatal familial insomnia depend on PRNP codon 129 methionine-valine polymorphism?
    Rupprecht S, Grimm A, Schultze T, Zinke J, Karvouniari P, Axer H, Witte OW, Schwab M.
    J Clin Sleep Med; 2013 Dec 15; 9(12):1343-5. PubMed ID: 24340298
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  • 17. Clinical, histopathological and genetic studies in a case of fatal familial insomnia with review of the literature.
    Peng B, Zhang S, Dong H, Lu Z.
    Int J Clin Exp Pathol; 2015 Dec 15; 8(9):10171-7. PubMed ID: 26617725
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  • 18. The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred.
    McLean CA, Storey E, Gardner RJ, Tannenberg AE, Cervenáková L, Brown P.
    Neurology; 1997 Aug 15; 49(2):552-8. PubMed ID: 9270595
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  • 19. [Fatal familial insomnia--a rare differential diagnosis in dementia].
    Friedrich M, Körte R, Portero C, Arzberger T, Kretzschmar HA, Zerr I, Nacimiento W.
    Fortschr Neurol Psychiatr; 2008 Jan 15; 76(1):36-40. PubMed ID: 18189221
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  • 20. Fatal familial insomnia: clinical and pathologic study of five new cases.
    Manetto V, Medori R, Cortelli P, Montagna P, Tinuper P, Baruzzi A, Rancurel G, Hauw JJ, Vanderhaeghen JJ, Mailleux P.
    Neurology; 1992 Feb 15; 42(2):312-9. PubMed ID: 1736158
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