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Journal Abstract Search

165 related items for PubMed ID: 9669714

  • 1. Conclusions of the symposium.
    Gambetti P, Lugaresi E.
    Brain Pathol; 1998 Jul; 8(3):571-5. PubMed ID: 9669714
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  • 2. 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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  • 3. 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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  • 4. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.
    Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E.
    Brain Pathol; 1995 Jan 10; 5(1):43-51. PubMed ID: 7767490
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  • 5. [Fatal familial insomnia].
    Delisle MB, Uro-Coste E, Gray F, Vital C.
    Clin Exp Pathol; 1999 Jan 10; 47(3-4):176-80. PubMed ID: 10472737
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  • 6. 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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  • 15. Fatal familial insomnia: clinical and pathologic heterogeneity in genetic half brothers.
    Johnson MD, Vnencak-Jones CL, McLean MJ.
    Neurology; 1998 Dec 10; 51(6):1715-7. PubMed ID: 9855529
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  • 16. 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 Dec 10; 9(3):228-35. PubMed ID: 26074146
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  • 18. The pathophysiology of fatal familial insomnia.
    Lugaresi E, Tobler I, Gambetti P, Montagna P.
    Brain Pathol; 1998 Jul 10; 8(3):521-6. PubMed ID: 9669702
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  • 20. Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: first report from Japan.
    Nagayama M, Shinohara Y, Furukawa H, Kitamoto T.
    Neurology; 1996 Nov 10; 47(5):1313-6. PubMed ID: 8909448
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