AOJS - de Michele,G.; Pocchiari,M.; Petraroli,R.; Manfredi,M.; Caneve,G.; Coppola,G.; Casali,C.; Sacca,F.; Piccardo,P.; Salvatore,E.; Berardelli,A.; Orio,M.; Barbieri,F.; Ghetti,B.; Filla,A. - Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family - Canadian Journal of Neurological Sciences 2003 Aug; 30(3): 233-6
AAYS - Barbanti,P.; Fabbrini,G.; Salvatore,M.; Petraroli,R.; Cardone,F.; Maras,B.; Equestre,M.; Macchi,G.; Lenzi,G.L.; Pocchiari,M. - Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation) - Neurology 1996 Sep; 47(3): 734-41
APCN - Barbanti,P.; Fabbrini,G.; Salvatore,M.; Petraroli,R.; Pocchiari,M.; Macchi,G.; Lenzi,G.L. - Phenotypic heterogeneity in Gerstmann-Sträussler-Scheinker syndrome with codon-102 mutation of the prion protein gene is not related to codon-129 polymorphism - Annals of Neurology 1994; 36(N2): 309-309
AGYV - Ladogana,A.; Casaccia,P.; Ingrosso,L.; Cibati,M.; Salvatore,M.; Xi,Y.G.; Masullo,C.; Pocchiari,M. - Sulphate polyanions prolong the incubation period of scrapie-infected hamsters - Journal of General Virology 1992 Mar; 73(3): 661-5
AIAT - Masullo,C.; Salvatore,M.; Macchi,G.; Genuardi,M.; Pocchiari,M. - Progressive dementia in a young patient with a homozygous deletion of the PrP gene - Annals of the New York Academy of Sciences 1994 Jun 6; 724: 358-60
AJMH - Pocchiari,M.; Salvatore,M.; Cutruzzola,F.; Genuardi,M.; Allocatelli,C.T.; Masullo,C.; Macchi,G.; Alema,G.; Galgani,S.; Xi,Y.G.; et al. - A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease - Annals of Neurology 1993 Dec; 34(6): 802-7
AJMI - Pocchiari,M.; Masullo,C.; Salvatore,M.; Genuardi,M.; Galgani,S. - Creutzfeldt-Jakob disease after non-commercial dura mater graft - Lancet 1992 Sep 5; 340(8819): 614-5
AJMJ - Pocchiari,M.; Salvatore,M.; Ladogana,A.; Ingrosso,L.; Xi,Y.G.; Cibati,M.; Masullo,C. - Experimental drug treatment of scrapie: a pathogenetic basis for rationale therapeutics. - European Journal of Epidemiology 1991 Sep; 7(5): 556-61
AKIX - Salvatore,M.; Seeber,A.C.; Nacmias,B.; Petraroli,R.; Sorbi,S.; Pocchiari,M. - Alpha1 antichymotrypsin signal peptide polymorphism in sporadic Creutzfeldt-Jakob disease - Neuroscience Letters 1997 May 16; 227(2): 140-2
AKIY - Salvatore,M.; Pocchiari,M.; Cardone,F.; Petraroli,R.; D'Alessandro,M.; Galvez,S.; Brown,P.; Macchi,G.; Fieschi,C.; Colosimo,C. - Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob disease - Journal of Neurology, Neurosurgery and Psychiatry 1996 Jul; 61(1): 111-2
AKIZ - Salvatore,M.; Seeber,A.C.; Nacmias,B.; Petraroli,R.; D'Alessandro,M.; Sorbi,S.; Pocchiari,M. - Apolipoprotein E in sporadic and familial Creutzfeldt-Jakob disease - Neuroscience Letters 1995 Oct 20; 199(2): 95-8
ANBF - Salvatore,M.; Genuardi,M.; Petraroli,R.; Masullo,C.; D'Alessandro,M.; Pocchiari,M. - Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease (vol 94, pg 375, 1994) - Human Genetics 1995 May; 95(5): 605
AKJA - Salvatore,M.; Genuardi,M.; Petraroli,R.; Masullo,C.; D'Alessandro,M.; Pocchiari,M. - Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease - Human Genetics 1994 Oct; 94(4): 375-9