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Journal Abstract Search

240 related items for PubMed ID: 9528048

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  • 3. [Fatal familial insomnia and prion diseases].
    Seilhean D, Duyckaerts C, Hauw JJ.
    Rev Neurol (Paris); 1995 Apr; 151(4):225-30. PubMed ID: 7481372
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  • 5. [Fatal familial insomnia].
    Delisle MB, Uro-Coste E, Gray F, Vital C.
    Clin Exp Pathol; 1999 Apr; 47(3-4):176-80. PubMed ID: 10472737
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  • 6. [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; 153(4):239-43. PubMed ID: 9296141
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  • 8. Regional distribution of protease-resistant prion protein in fatal familial insomnia.
    Parchi P, Castellani R, Cortelli P, Montagna P, Chen SG, Petersen RB, Manetto V, Vnencak-Jones CL, McLean MJ, Sheller JR.
    Ann Neurol; 1995 Jul; 38(1):21-9. PubMed ID: 7611720
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  • 10. Fatal familial insomnia: clinical features and molecular genetics.
    Cortelli P, Gambetti P, Montagna P, Lugaresi E.
    J Sleep Res; 1999 Jun; 8 Suppl 1():23-9. PubMed ID: 10389103
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  • 11. First experimental transmission of fatal familial insomnia.
    Tateishi J, Brown P, Kitamoto T, Hoque ZM, Roos R, Wollman R, Cervenáková L, Gajdusek DC.
    Nature; 1995 Aug 03; 376(6539):434-5. PubMed ID: 7630420
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  • 13. Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
    Nitrini R, Rosemberg S, Passos-Bueno MR, da Silva LS, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBlanc A.
    Ann Neurol; 1997 Aug 03; 42(2):138-46. PubMed ID: 9266722
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  • 14. [Fatal familiar insomnia: clinical, neurophysiological and histopathological study of two cases].
    Ayuso Blanco T, Urriza Mena J, Caballero Martínez C, Iriarte Franco J, Munoz R, García-Bragado F.
    Neurologia; 2006 Oct 03; 21(8):414-20. PubMed ID: 17013786
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  • 16. Selective neuronal vulnerability in human prion diseases. Fatal familial insomnia differs from other types of prion diseases.
    Guentchev M, Wanschitz J, Voigtländer T, Flicker H, Budka H.
    Am J Pathol; 1999 Nov 03; 155(5):1453-7. PubMed ID: 10550300
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  • 17. 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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  • 20. One gene, two diseases and three conformations: molecular dynamics simulations of mutants of human prion protein at room temperature and elevated temperatures.
    Shamsir MS, Dalby AR.
    Proteins; 2005 May 01; 59(2):275-90. PubMed ID: 15739202
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