AQRW - Piccardo,P.; Young,K.; Jones,C.K.; Seiler,C.; Lazzarini,A.; Golbe,L.I.; Zimmerman,T.R.Jr.; Dickson,D.W.; Vinters,H.V.; Lennox,A.; Perlman,S.L.; McLachlan,D.C.; St George-Hyslop,P.; Giaccone,G.; Bugiani,O.; Tagliavini,F.; Dlouhy,S.R.; Ghetti,B. - GerstmannSträussler-Scheinker (gss) disease (p102l) - prion protein (prp) core deposits are best recognized by antibodies directed to epitopes spanning prp residues 90-165 - Journal of Neuropathology and Experimental Neurology 1995; 54(3): 448 Abstraktnummer 149
AUYR - Rogaeva,E.; Zadikoff,C.; Ponesse,J.; Schmitt-Ulms,G.; Kawarai,T.; Sato,C.; Salehi-Rad,S.; St George-Hyslop,P.; Lang,A.E. - Childhood onset in familial prion disease with a novel mutation in the PRNP gene - Archives of Neurology 2006 Jul; 63(7): 1016-21
AMWV - Young,K.; Jones,C.K.; Piccardo,P.; Lazzarini,A.; Golbe,L.I.; Zimmerman,T.R.Jr.; Dickson,D.W.; Mclachlan,D.C.; St George-Hyslop,P.; Lennox,A.; Perlman,S.; Vinters,H.V.; Hodes,M.E.; Dlouhy,S.; Ghetti,B. - Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients - Neurology 1995 Jun; 45(6): 1127-34