AHTJ - Manetto,V.; Medori,R.; Cortelli,P.; Montagna,P.; Tinuper,P.; Baruzzi,A.; Rancurel,G.; Hauw,J.J.; Vanderhaeghen,J.J.; Mailleux,P.; Bugiani,O.; Tagliavini,F.; Bouras,C.; Rizzuto,N.; Lugaresi,E.; Gambetti,P. - Fatal familial insomnia: clinical and pathologic study of five new cases. - Neurology 1992 Feb; 42(2): 312-9
AIGH - Medori,R.; Tritschler,H.J.; LeBlanc,A.; Villare,F.; Manetto,V.; Chen,H.Y.; Xue,R.; Leal,S.; Montagna,P.; Cortelli,P.; et al. - Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene - The New England Journal of Medicine 1992 Feb 13; 326(7): 444-9
AJFA - Parchi,P.; Castellani,R.J.; Cortelli,P.; Montagna,P.; Chen,S.G.; Petersen,R.B.; Manetto,V.; Vnencak-Jones,C.L.; McLean,M.J.; Sheller,J.R.; Lugaresi,E.; Autilio-Gambetti,L.; Gambetti,P. - Regional distribution of protease-resistant prion protein in fatal familial insomnia - Annals of Neurology 1995 Jul; 38(1): 21-9
AJKG - Petersen,R.B.; Tabaton,M.; Chen,S.G.; Monari,L.; Richardson,S.L.; Lynch,T.; Manetto,V.; Lanska,D.J.; Markesbery,W.R.; Currier,R.D.; Autilio-Gambetti,L.; Wilhelmsen,K.C.; Gambetti,P. - Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17. - Neurology 1995 Jun; 45(6): 1062-7