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Journal Abstract Search

96 related items for PubMed ID: 10637858

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  • 2. [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; 25(148):2006-14. PubMed ID: 9528048
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  • 4. Absence of sleep EEG markers in fatal familial insomnia healthy carriers: a spectral analysis study.
    Ferrillo F, Plazzi G, Nobili L, Beelke M, De Carli F, Cortelli P, Tinuper P, Avoni P, Vandi S, Gambetti P, Lugaresi E, Montagna P.
    Clin Neurophysiol; 2001 Oct; 112(10):1888-92. PubMed ID: 11595148
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  • 8. 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 Oct; 9(3):228-35. PubMed ID: 26074146
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  • 9. [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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  • 12. Familial and sporadic fatal insomnia.
    Montagna P, Gambetti P, Cortelli P, Lugaresi E.
    Lancet Neurol; 2003 Mar; 2(3):167-76. PubMed ID: 12849238
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  • 16. Fatal familial insomnia: a model disease in sleep physiopathology.
    Montagna P.
    Sleep Med Rev; 2005 Oct; 9(5):339-53. PubMed ID: 16109494
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  • 18. Effect of the prion 129 polymorphism on nocturnal sleep and insomnia complaints: a population-based study.
    Pedrazzoli M, Ling L, Young TB, Finn L, Tufik S, Mignot E.
    J Sleep Res; 2002 Dec; 11(4):357-8. PubMed ID: 12464104
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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; 76(1):36-40. PubMed ID: 18189221
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