AAVU - Avoni,P.; Cortelli,P.; Montagna,P.; Tinuper,P.; Sforza,E.; Contin,M.; Parchi,P.; Pierangeli,G.; Maltoni,P.; Pavani,A.; et al. - Circadian hormonal rhythms in two new cases of fatal familial insomnia - Acta Neurologica 1991 Dec; 13(6): 574-6
ADCB - de Leon,M.J.; Convit,A.; DeSanti,S.; Golomb,J.; Tarshish,C.; Rusinek,H.; Bobinski,M.; Ince,C.; Miller,D.C.; Wisniewski,H.M.; et al. - The hippocampus in aging and Alzheimer's disease - Neuroimaging Clinics of North America 1995 Feb; 5(1): 1-17
AQDX - Ghetti,B.; Piccardo,P.; Ichimiya,Y.; Goedert,M.; Kitamoto,T.; Tateishi,J.; Spillantini,M.G.; Frangione,B.; Bugiani,O.; Giaccone,G.; Prelli,F.; Dlouhy,S.R.; et al. - Prion protein amyloid angiopathy and Alzheimer neurofibrillary tangles in prnp stop codon-145 - Journal of Neuropathology and Experimental Neurology 1995; 54(N3): 415
AEMY - Ghetti,B.; Tagliavini,F.; Masters,C.L.; Beyreuther,K.; Giaccone,G.; Verga,L.; Farlow,M.R.; Conneally,P.M.; Dlouhy,S.R.; Azzarelli,B.; et al. - Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family. - Neurology 1989 Nov; 39(11): 1453-61
AERA - Goldfarb,L.G.; Brown,P.; Haltia,M.; Cathala,F.; McCombie,W.R.; Kovanen,J.; Cervenakova,L.; Goldin,L.; Nieto,A.; Godec,M.S.; et al. - Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin - Annals of Neurology 1992 Mar; 31(3): 274-81
AWGI - Hagiwara,K.; Nakamura,Y.; Yamakawa,Y.; Sato,Y.; Tobiume,M.; Sata,T.; et al. - Expert Committee for BSE Diagnosis, Ministry of Health, Labour and Welfare (MHLW) - Studies on the second atypical BSE case in a Japanese black cow - International Conference - Prion 2006: Strategies, advances and trends towards protection of society - 3.10.-6.10.2006, Torino, Italy, Lingotto Conference Centre - Poster sessions PR-18
AFWV - Iwabuchi,K.; Endoh,S.; Hagimoto,H.; Okamoto,K.; Miyakawa,T.; Yamaguchi,T.; Kajiwara,A.; Inoue,K.; Yamada,Y.; Amano,N.; et al. - [Three patients from two families with familial Creutzfeldt-Jakob disease having a point mutation in the prion protein gene at codon 200 (Glu -> Lys)] - No to Shinkei. Brain and Nerve 1994 Apr; 46(4): 349-54
AHAH - Lantos,P.L.; McGill,I.S.; Janota,I.; Doey,L.J.; Collinge,J.; Bruce,M.T.; Whatley,S.A.; Anderton,B.H.; Clinton,J.; Roberts,G.W.; et al. - Prion protein immunocytochemistry helps to establish the true incidence of prion diseases - Neuroscience Letters 1992 Nov 23; 147(1): 67-71
ASCN - Lin,S.H.; Zhao,J.X.; Jiang,X.M.; et al. - Clinicopathological, immunohistochemical and transmission studies of Creutzfeldt-Jakob disease - Zhonghua shen jing ke za zhi (Chinese Journal of Neurology) 1996; 29: 29-32
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
AINW - Mora,C.A.; Garruto,R.M.; Brown,P.; Guiroy,D.; Morgan,O.S.; Rodgers-Johnson,P.; Ceroni,M.; Yanagihara,R.; Goldfarb,L.G.; Gibbs,C.J.Jr.; et al. - Seroprevalence of antibodies to HTLV-I in patients with chronic neurological disorders other than tropical spastic paraparesis - Annals of Neurology 1988; 23 Suppl: S192-5
AIRU - Nagano,K.; Miki,T.; Yoshioka,K.; Katsumi,D.; Katsuya,T.; Takeda,M.; Ikeda,M.; Tanabe,H.; Nishimura,T.; Sakai,Y.; et al. - [Two kindreds with familial Alzheimer's disease - analysis of the APP717 mutation and the mutated genes for the prion protein] - Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics 1992 Jun; 29(6): 509-14
AJAS - Ono,S.; Fukunaga,M.; Otsuka,N.; Nagai,K.; Morita,K.; Muranaka,A.; Furukawa,T.; Yanagimoto,S.; Tomomitsu,T.; Kawai,K.; et al. - [A case of Creutzfeldt-Jakob disease followed up by N-isopropyl-[123I]-p-iodoamphetamine and 99mTc-hexamethylpropyleneamine oxime SPECT] - Kaku Igaku. Japanese Journal of Nuclear Medicine 1989 Jan; 26(1): 77-88
AJAU - Onodera,A.; Ikeda,T.; Horiuchi,M.; Ishiguro,N.; Onuma,M.; Hirano,N.; Mikami,T.; Honda,E.; Hirai,K.; Kai,K.; Yugi,H.; Muramatsu,Y.; et al. - Survey of natural scrapie in Japan: analysis of RFLP types of the PrP gene and detection of PrPsc mainly in Suffolk sheep. - Journal of Veterinary Medical Science 1994 Aug; 56(4): 627-32
AJKI - Petersen,R.B.; Tabaton,M.; Berg,L.; Schrank,B.; Torack,R.M.; Leal,S.; Julien,J.; Vital,C.; Deleplanque,B.; Pendlebury,W.W.; et al. - Analysis of the prion protein gene in thalamic dementia - Neurology 1992 Oct; 42(10): 1859-63
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
AKMQ - Schellenberg,G.D.; Anderson,L.; O'dahl,S.; Wisjman,E.M.; Sadovnick,A.D.; Ball,M.J.; Larson,E.B.; Kukull,W.A.; Martin,G.M.; Roses,A.D.; et al. - APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease - American Journal of Human Genetics 1991 Sep; 49(3): 511-7
AKUW - Shishido,F.; Uemura,K.; Inugami,A.; Tomura,N.; Higano,S.; Fujita,H.; Tabata,K.; Sasaki,H.; Murakami,M.; Kanno,I.; et al. - [Brain glucose metabolism in a patient with Creutzfeldt-Jakob disease measured by positron emission tomography] - Kaku Igaku. Japanese Journal of Nuclear Medicine 1990 Jun; 27(6): 649-54
ALKP - Taratuto,A.L.; Piccardo,P.; Leiguarda,R.; Granillo,R.; Monti,A.; Scarlatti,A.; Leits,A.; Morasso,C.; Marquez Vigo,C.; Vila,J.; et al. - Creutzfeldt-Jakob disease. Report of 10 neuropathologically-verified cases in Argentina. - Medicina (Buenos Aires) 1989; 49(4): 293-303
ARWO - Taylor,D.M.; et al. - Deactivation of the scrapie agent by simulated rendering methods - unbekannt
AMUG - Yamada,M.; Itoh,Y.; Fujigasaki,H.; Naruse,S.; Kaneko,K.; Kitamoto,T.; Tateishi,J.; Otomo,E.; Hayakawa,M.; Tanaka,J.; et al. - A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease - Neurology 1993 Dec; 43(12): 2723-4