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176 related items for PubMed ID: 15634234

  • 1. Fatal familial insomnia with an unusual prion protein deposition pattern: an autopsy report with an experimental transmission study.
    Sasaki K, Doh-ura K, Wakisaka Y, Tomoda H, Iwaki T.
    Neuropathol Appl Neurobiol; 2005 Feb; 31(1):80-7. PubMed ID: 15634234
    [Abstract] [Full Text] [Related]

  • 2. Fatal familial insomnia: the first account in a family of Chinese descent.
    Spacey SD, Pastore M, McGillivray B, Fleming J, Gambetti P, Feldman H.
    Arch Neurol; 2004 Jan; 61(1):122-5. PubMed ID: 14732629
    [Abstract] [Full Text] [Related]

  • 3. 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; 251(6):715-24. PubMed ID: 15311348
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Increased expression of water channel aquaporin 1 and aquaporin 4 in Creutzfeldt-Jakob disease and in bovine spongiform encephalopathy-infected bovine-PrP transgenic mice.
    Rodríguez A, Pérez-Gracia E, Espinosa JC, Pumarola M, Torres JM, Ferrer I.
    Acta Neuropathol; 2006 Nov; 112(5):573-85. PubMed ID: 16871401
    [Abstract] [Full Text] [Related]

  • 6. Loss of glycosylation associated with the T183A mutation in human prion disease.
    Grasbon-Frodl E, Lorenz H, Mann U, Nitsch RM, Windl O, Kretzschmar HA.
    Acta Neuropathol; 2004 Dec; 108(6):476-84. PubMed ID: 15558291
    [Abstract] [Full Text] [Related]

  • 7. An autopsy case of Creutzfeldt-Jakob disease with a V180I mutation of the PrP gene and Alzheimer-type pathology.
    Yoshida H, Terada S, Ishizu H, Ikeda K, Hayabara T, Ikeda K, Deguchi K, Touge T, Kitamoto T, Kuroda S.
    Neuropathology; 2010 Apr; 30(2):159-64. PubMed ID: 19703264
    [Abstract] [Full Text] [Related]

  • 8. Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.
    Gelpi E, Kovacs GG, Ströbel T, Koperek O, Voigtländer T, Liberski PP, Budka H.
    Acta Neuropathol; 2005 Nov; 110(5):513-9. PubMed ID: 16155763
    [Abstract] [Full Text] [Related]

  • 9. Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease.
    Sasaki K, Doh-ura K, Furuta A, Nakashima S, Morisada Y, Tateishi J, Iwaki T.
    Acta Neuropathol; 2003 Jul; 106(1):92-6. PubMed ID: 12682740
    [Abstract] [Full Text] [Related]

  • 10. Correlative studies support lipid peroxidation is linked to PrP(res) propagation as an early primary pathogenic event in prion disease.
    Brazier MW, Lewis V, Ciccotosto GD, Klug GM, Lawson VA, Cappai R, Ironside JW, Masters CL, Hill AF, White AR, Collins S.
    Brain Res Bull; 2006 Jan 30; 68(5):346-54. PubMed ID: 16377442
    [Abstract] [Full Text] [Related]

  • 11. [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 30; 76(1):36-40. PubMed ID: 18189221
    [Abstract] [Full Text] [Related]

  • 12. [Usefulness of molecular genetic analysis of the PRNP gene in patients with cerebellar ataxia: a new case of fatal familial insomnia].
    Marcaud V, Laplanche JL, Defontaines B, Beaudry P, Vital A, Vincent D, Sazdovitch V, Hauw JJ, Latinville D, Jung P, Vecchierini F, Degos CF.
    Rev Neurol (Paris); 2003 Feb 30; 159(2):199-202. PubMed ID: 12660573
    [Abstract] [Full Text] [Related]

  • 13. Clinical, histopathological and genetic studies in a family with fatal familial insomnia.
    Shi XH, Han J, Zhang J, Shi Q, Chen JM, Xia SL, Xie ZQ, Shen XJ, Shan B, Lei YJ, Shi S, Zhou W, Zhang BY, Gao C, Liu YH, Song J, Guo YJ, Wang DX, Xu BL, Dong XP.
    Infect Genet Evol; 2010 Mar 30; 10(2):292-7. PubMed ID: 20096809
    [Abstract] [Full Text] [Related]

  • 14. [Fatal familial insomnia].
    Delisle MB, Uro-Coste E, Gray F, Vital C.
    Clin Exp Pathol; 1999 Mar 30; 47(3-4):176-80. PubMed ID: 10472737
    [Abstract] [Full Text] [Related]

  • 15. Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.
    Roeber S, Krebs B, Neumann M, Windl O, Zerr I, Grasbon-Frodl EM, Kretzschmar HA.
    Acta Neuropathol; 2005 Apr 30; 109(4):443-8. PubMed ID: 15739100
    [Abstract] [Full Text] [Related]

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  • 17. [Fatal familial insomnia and prion diseases].
    Seilhean D, Duyckaerts C, Hauw JJ.
    Rev Neurol (Paris); 1995 Apr 30; 151(4):225-30. PubMed ID: 7481372
    [Abstract] [Full Text] [Related]

  • 18. Characterisation of new monoclonal antibodies reacting with prions from both human and animal brain tissues.
    Cordes H, Bergström AL, Ohm J, Laursen H, Heegaard PM.
    J Immunol Methods; 2008 Sep 15; 337(2):106-20. PubMed ID: 18657541
    [Abstract] [Full Text] [Related]

  • 19. [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 15; 25(148):2006-14. PubMed ID: 9528048
    [Abstract] [Full Text] [Related]

  • 20. Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report.
    Moody KM, Schonberger LB, Maddox RA, Zou WQ, Cracco L, Cali I.
    BMC Neurol; 2011 Oct 31; 11():136. PubMed ID: 22040318
    [Abstract] [Full Text] [Related]

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