These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
12. 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 [TBL] [Abstract][Full Text] [Related]
13. Tubulovesicular structures are a consistent (and unexplained) finding in the brains of humans with prion diseases. Liberski PP; Sikorska B; Hauw JJ; Kopp N; Streichenberger N; Giraud P; Budka H; Boellaard JW; Brown P Virus Res; 2008 Mar; 132(1-2):226-8. PubMed ID: 18164506 [TBL] [Abstract][Full Text] [Related]
14. Selective neuronal vulnerability in human prion diseases. Fatal familial insomnia differs from other types of prion diseases. Guentchev M; Wanschitz J; Voigtländer T; Flicker H; Budka H Am J Pathol; 1999 Nov; 155(5):1453-7. PubMed ID: 10550300 [TBL] [Abstract][Full Text] [Related]
15. [Expanded illness spectrum of human spongiform encephalopathies or prion diseases]. Weber T; Zerr I; Bodemer M; Poser S Nervenarzt; 1997 Apr; 68(4):309-23. PubMed ID: 9273460 [TBL] [Abstract][Full Text] [Related]