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Journal Abstract Search

168 related items for PubMed ID: 10389103

  • 1. 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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  • 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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  • 5. The pathophysiology of fatal familial insomnia.
    Lugaresi E, Tobler I, Gambetti P, Montagna P.
    Brain Pathol; 1998 Jul; 8(3):521-6. PubMed ID: 9669702
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  • 6. Molecular pathology of fatal familial insomnia.
    Parchi P, Petersen RB, Chen SG, Autilio-Gambetti L, Capellari S, Monari L, Cortelli P, Montagna P, Lugaresi E, Gambetti P.
    Brain Pathol; 1998 Jul; 8(3):539-48. PubMed ID: 9669705
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  • 7. Identification of new molecular alterations in fatal familial insomnia.
    Llorens F, Thüne K, Schmitz M, Ansoleaga B, Frau-Méndez MA, Cramm M, Tahir W, Gotzmann N, Berjaoui S, Carmona M, Silva CJ, Fernandez-Vega I, José Zarranz J, Zerr I, Ferrer I.
    Hum Mol Genet; 2016 Jun 15; 25(12):2417-2436. PubMed ID: 27056979
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  • 8. A subtype of sporadic prion disease mimicking fatal familial insomnia.
    Parchi P, Capellari S, Chin S, Schwarz HB, Schecter NP, Butts JD, Hudkins P, Burns DK, Powers JM, Gambetti P.
    Neurology; 1999 Jun 10; 52(9):1757-63. PubMed ID: 10371520
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  • 9. Familial and sporadic fatal insomnia.
    Montagna P, Gambetti P, Cortelli P, Lugaresi E.
    Lancet Neurol; 2003 Mar 10; 2(3):167-76. PubMed ID: 12849238
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  • 14. 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 10; 112(10):1888-92. PubMed ID: 11595148
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  • 15. 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 10; 53(4):822-7. PubMed ID: 8105681
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  • 17. Fatal familial insomnia in a new Italian kindred.
    Padovani A, D'Alessandro M, Parchi P, Cortelli P, Anzola GP, Montagna P, Vignolo LA, Petraroli R, Pocchiari M, Lugaresi E, Gambetti P.
    Neurology; 1998 Nov 10; 51(5):1491-4. PubMed ID: 9818894
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  • 18. [Sleep disorders associated to prion diseases].
    Merino-Ramírez MA, Escudero-Torrella M.
    Rev Neurol; 1998 Nov 10; 31(2):147-51. PubMed ID: 10951672
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  • 19. Fatal familial insomnia: sleep, neuroendocrine and vegetative alterations.
    Montagna P, Cortelli P, Gambetti P, Lugaresi E.
    Adv Neuroimmunol; 1995 Nov 10; 5(1):13-21. PubMed ID: 7795890
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  • 20. Conclusions of the symposium.
    Gambetti P, Lugaresi E.
    Brain Pathol; 1998 Jul 10; 8(3):571-5. PubMed ID: 9669714
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