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156 related items for PubMed ID: 35419959

  • 1. Can insomnia be fatal? An Australian case of fatal familial insomnia.
    Habteslassie D, McMahon M, Wimaleswaran H.
    Intern Med J; 2022 Apr; 52(4):667-670. PubMed ID: 35419959
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  • 2. A case of fatal familial insomnia: diagnostic and therapeutic approaches.
    Rose DK, Liu AJ.
    Neurocase; 2022 Feb; 28(1):131-134. PubMed ID: 35037601
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  • 3. Fatal insomnia: the elusive prion disease.
    Patel D, Ibrahim H, Rankin J, Hilton D, Barria MA, Ritchie DL, Smith C, Zeman A.
    BMJ Case Rep; 2021 Jun 22; 14(6):. PubMed ID: 34158325
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  • 4. 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
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  • 5. A proposal of new diagnostic pathway for fatal familial insomnia.
    Krasnianski A, Sanchez Juan P, Ponto C, Bartl M, Heinemann U, Varges D, Schulz-Schaeffer WJ, Kretzschmar HA, Zerr I.
    J Neurol Neurosurg Psychiatry; 2014 Jun 15; 85(6):654-9. PubMed ID: 24249784
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  • 7. [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
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  • 11. Analysis of a large case series of fatal familial insomnia to determine tests with the highest diagnostic value.
    Kortazar-Zubizarreta I, Eraña H, Pereda A, Charco JM, Manero-Azua A, Ruiz-Onandi R, Aguirre U, Gonzalez-Chinchon G, Basque Prionopathies Study Group, Perez de Nanclares G, Castilla J.
    J Neuropathol Exp Neurol; 2023 Jan 20; 82(2):169-179. PubMed ID: 36458954
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  • 14. [Fatal familial insomnia and prion diseases].
    Seilhean D, Duyckaerts C, Hauw JJ.
    Rev Neurol (Paris); 1995 Apr 20; 151(4):225-30. PubMed ID: 7481372
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  • 15. 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 20; 13(1):116-123. PubMed ID: 31122137
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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 Jan 20; 9(3):228-35. PubMed ID: 26074146
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  • 20. Fatal Familial Insomnia: Clinical Aspects and Molecular Alterations.
    Llorens F, Zarranz JJ, Fischer A, Zerr I, Ferrer I.
    Curr Neurol Neurosci Rep; 2017 Apr 20; 17(4):30. PubMed ID: 28324299
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