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281 related items for PubMed ID: 26074146

  • 1. 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; 9(3):228-35. PubMed ID: 26074146
    [Abstract] [Full Text] [Related]

  • 2. Does the clinical phenotype of fatal familial insomnia depend on PRNP codon 129 methionine-valine polymorphism?
    Rupprecht S, Grimm A, Schultze T, Zinke J, Karvouniari P, Axer H, Witte OW, Schwab M.
    J Clin Sleep Med; 2013 Dec 15; 9(12):1343-5. PubMed ID: 24340298
    [Abstract] [Full Text] [Related]

  • 3. 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 15; 31(1):81-90. PubMed ID: 23175354
    [Abstract] [Full Text] [Related]

  • 4. Clinical features and genetic characteristics of two Chinese pedigrees with fatal family insomnia.
    He R, Hu Y, Yao L, Tian Y, Zhou Y, Yi F, Zhou L, Xu H, Sun Q.
    Prion; 2019 Jan 15; 13(1):116-123. PubMed ID: 31122137
    [Abstract] [Full Text] [Related]

  • 5. Clinical, histopathological and genetic studies in a case of fatal familial insomnia with review of the literature.
    Peng B, Zhang S, Dong H, Lu Z.
    Int J Clin Exp Pathol; 2015 Jan 15; 8(9):10171-7. PubMed ID: 26617725
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 251(6):715-24. PubMed ID: 15311348
    [Abstract] [Full Text] [Related]

  • 7. Fatal familial insomnia and sporadic fatal insomnia.
    Cracco L, Appleby BS, Gambetti P.
    Handb Clin Neurol; 2018 Jun 15; 153():271-299. PubMed ID: 29887141
    [Abstract] [Full Text] [Related]

  • 8. Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
    Marcon G, Indaco A, Di Fede G, Suardi S, Finato N, Moretti V, Micoli S, Fociani P, Zerbi P, Pincherle A, Redaelli V, Tagliavini F, Giaccone G.
    Brain Pathol; 2014 Mar 15; 24(2):148-51. PubMed ID: 24118545
    [Abstract] [Full Text] [Related]

  • 9. In vivo detection of thalamic gliosis: a pathoradiologic demonstration in familial fatal insomnia.
    Haïk S, Galanaud D, Linguraru MG, Peoc'h K, Privat N, Faucheux BA, Ayache N, Hauw JJ, Dormont D, Brandel JP.
    Arch Neurol; 2008 Apr 15; 65(4):545-9. PubMed ID: 18413481
    [Abstract] [Full Text] [Related]

  • 10. [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 15; 76(1):36-40. PubMed ID: 18189221
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 10(2):292-7. PubMed ID: 20096809
    [Abstract] [Full Text] [Related]

  • 12. Does the prion protein gene 129 codon polymorphism influence sleep? Evidence from a fatal familial insomnia kindred.
    Plazzi G, Montagna P, Beelke M, Nobili L, De Carli F, Cortelli P, Vandi S, Avoni P, Tinuper P, Gambetti P, Lugaresi E, Ferrillo F.
    Clin Neurophysiol; 2002 Dec 15; 113(12):1948-53. PubMed ID: 12464332
    [Abstract] [Full Text] [Related]

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  • 14. Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation.
    Rodríguez-Martínez AB, Alfonso-Sánchez MA, Peña JA, Sánchez-Valle R, Zerr I, Capellari S, Calero M, Zarranz JJ, de Pancorbo MM.
    Neurogenetics; 2008 May 15; 9(2):109-18. PubMed ID: 18347820
    [Abstract] [Full Text] [Related]

  • 15. Corticobasal manifestations of Creutzfeldt-Jakob disease with D178N-homozygous 129M genotype.
    Huang Y, Jianfang M, Morales R, Tang H.
    Prion; 2020 Dec 15; 14(1):232-237. PubMed ID: 32946318
    [Abstract] [Full Text] [Related]

  • 16. Thalamic contribution to Sleep Slow Oscillation features in humans: a single case cross sectional EEG study in Fatal Familial Insomnia.
    Gemignani A, Laurino M, Provini F, Piarulli A, Barletta G, d'Ascanio P, Bedini R, Lodi R, Manners DN, Allegrini P, Menicucci D, Cortelli P.
    Sleep Med; 2012 Aug 15; 13(7):946-52. PubMed ID: 22609023
    [Abstract] [Full Text] [Related]

  • 17. Reduced cerebral blood flow in genetic prion disease with PRNP D178N-129M mutation: an arterial spin labeling MRI study.
    Chen S, Guan M, Shang JK, He S, Zhang ML, Ma MM, Zhang JW.
    J Clin Neurosci; 2015 Jan 15; 22(1):204-6. PubMed ID: 25220284
    [Abstract] [Full Text] [Related]

  • 18. Familial and sporadic fatal insomnia.
    Montagna P, Gambetti P, Cortelli P, Lugaresi E.
    Lancet Neurol; 2003 Mar 15; 2(3):167-76. PubMed ID: 12849238
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 61(1):122-5. PubMed ID: 14732629
    [Abstract] [Full Text] [Related]

  • 20. [Clinical, neuroimaging and genetic features of two Chinese families with fatal familial insomnia].
    Bian Y, Wang S, Han XC, Yao S, Liu JG, Qi XK.
    Zhonghua Yi Xue Za Zhi; 2018 Aug 21; 98(31):2501-2504. PubMed ID: 30139003
    [Abstract] [Full Text] [Related]

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