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Journal Abstract Search

169 related items for PubMed ID: 9270595

  • 1. 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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  • 3. 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; 22(1):204-6. PubMed ID: 25220284
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  • 8. Phenotypic variability in fatal familial insomnia (D178N-129M) genotype.
    Zerr I, Giese A, Windl O, Kropp S, Schulz-Schaeffer W, Riedemann C, Skworc K, Bodemer M, Kretzschmar HA, Poser S.
    Neurology; 1998 Nov; 51(5):1398-405. PubMed ID: 9818868
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  • 9. Fatal familial insomnia and sporadic fatal insomnia.
    Cracco L, Appleby BS, Gambetti P.
    Handb Clin Neurol; 2018 Nov; 153():271-299. PubMed ID: 29887141
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  • 10. 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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  • 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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