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Journal Abstract Search


237 related items for PubMed ID: 15311348

  • 1. 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
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  • 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
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  • 4. [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. 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
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  • 6. 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
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  • 13. The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred.
    McLean CA, Storey E, Gardner RJ, Tannenberg AE, Cervenáková L, Brown P.
    Neurology; 1997 Aug; 49(2):552-8. PubMed ID: 9270595
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  • 14. [Fatal familial insomnia].
    Delisle MB, Uro-Coste E, Gray F, Vital C.
    Clin Exp Pathol; 1999 Aug; 47(3-4):176-80. PubMed ID: 10472737
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  • 15. Fatal familial insomnia and sporadic fatal insomnia.
    Cracco L, Appleby BS, Gambetti P.
    Handb Clin Neurol; 2018 Aug; 153():271-299. PubMed ID: 29887141
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  • 16. Fatal familial insomnia: Clinical features and early identification.
    Krasnianski A, Bartl M, Sanchez Juan PJ, Heinemann U, Meissner B, Varges D, Schulze-Sturm U, Kretzschmar HA, Schulz-Schaeffer WJ, Zerr I.
    Ann Neurol; 2008 May; 63(5):658-61. PubMed ID: 18360821
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  • 20. Prion mutation D178N with highly variable disease onset and phenotype.
    Synofzik M, Bauer P, Schöls L.
    J Neurol Neurosurg Psychiatry; 2009 Mar; 80(3):345-6. PubMed ID: 19228673
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