ACMP - Chapman,A.H.; Vieira e Silva,D. - Creutzfeldt-Jakob disease. A case report, with special attention to the electroencephalogram in this disorder and to its possible relationships to kuru, scrapie and "mad cow disease". - Arquivos de Neuro-Psiquiatria 1993 Jun; 51(2): 258-66
AQTX - Wallis,J.P.; Wells,A.W.; Matthews,J.N.; Chapman,C.E. - Long-term survival after blood transfusion: a population based study in the North of England. - Transfusion 2004 Jul; 44(7): 1025-32
AMSE - Wood,D.J.; Mason,J.B.; Chapman,H.M. - Scrapie scruples - New Zealand Veterinary Journal 1978 Jul; 26(7): 190-1
AOEE - Brown,P.; Chapman,J.C.; Cervenakova,L.; Goldfarb,L.G.; Korczyn,A.D. - Cell-free expression of the prnp gene containing a large insert associated with Creutzfeldt-Jakob-disease - Neurology 1996; 46(N2): S01.003
ACMQ - Chapman,J.C.; Cervenakova,L.; Petersen,R.B.; Lee,H.S.; Estupinan,J.; Richardson,S.; Vnencak-Jones,C.L.; Gajdusek,D.C.; Korczyn,A.D.; Brown,P.; Goldfarb,L.G. - APOE in non-Alzheimer amyloidoses: transmissible spongiform encephalopathies. - Neurology 1998 Aug; 51(2): 548-53
ACMR - Chapman,J.C.; Arlazoroff,A.; Goldfarb,L.G.; Cervenakova,L.; Neufeld,M.Y.; Werber,E.; Herbert,M.; Brown,P.; Gajdusek,D.C.; Korczyn,A.D. - Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation - Neurology 1996 Mar; 46(3): 758-61
ACMS - Chapman,J.C.; Ben-Israel,J.; Goldhammer,Y.; Korczyn,A.D. - The risk of developing Creutzfeldt-Jakob disease in subjects with the PRNP gene codon 200 point mutation - Neurology 1994 Sep; 44(9): 1683-6
ACMT - Chapman,J.C.; Brown,P.; Goldfarb,L.G.; Arlazoroff,A.; Gajdusek,D.C.; Korczyn,A.D. - Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation - Journal of Neurology, Neurosurgery and Psychiatry 1993 Oct; 56(10): 1109-12
ACMU - Chapman,J.C.; Brown,P.; Rabey,J.M.; Goldfarb,L.G.; Inzelberg,R.; Gibbs,C.J.Jr.; Gajdusek,D.C.; Korczyn,A.D. - Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation - Neurology 1992 Jun; 42(6): 1249-50
ACMV - Chapman,J.C.; Korczyn,A.D. - Genetic and environmental factors determining the development of Creutzfeldt-Jakob disease in Libyan Jews - Neuroepidemiology 1991; 10(5-6): 228-31
AEFQ - Frenkel,Y.R.; Ben-Israel,J.; Korczyn,A.D.; Chapman,J.C. - Penetrance and phenotypic expression of a mutation linked to Creutzfeldt-Jakob disease in the elderly - Dementia and Geriatric Cognitive Disorders 1999 Jan-Feb; 10(1): 47-50
AVWK - Fulbright,R.K.; Kingsley,P.B.; Guo,X.; Hoffmann,C.; Kahana,E.; Chapman,J.C.; Prohovnik,I. - The imaging appearance of Creutzfeldt-Jakob disease caused by the E200K mutation - Magnetic Resonance Imaging 2006 Nov; 24(9): 1121-9
AWFL - Gigi,A.; Kahana,E.; Prohovnik,I.; Chapman,J.C. - Long lasting familial Creutzfeldt-Jakob Disease without dementia: a case study - 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-15
AQED - Goldfarb,L.G.; Chapman,J.C.; Brown,P.; Cervenakova,L.; Gajdusek,D.C.; Korczyn,A.D. - Apolipoprotein-e genotype in human spongiform encephalopathies - Neurology 1996; 46(N2): 2064
AERC - Goldfarb,L.G.; Brown,P.; Mitrova,E.; Cervenakova,L.; Goldin,L.; Korczyn,A.D.; Chapman,J.C.; Galvez,S.; Cartier,L.R.; Rubenstein,R.; Gajdusek,D.C. - Creutzfeldt-Jakob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families. - European Journal of Epidemiology 1991 Sep; 7(5): 477-86
AERE - Goldfarb,L.G.; Korczyn,A.D.; Brown,P.; Chapman,J.C.; Gajdusek,D.C. - Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin - Lancet 1990 Sep 8; 336(8715): 637-8
AGRT - Korczyn,A.D.; Chapman,J.C.; Belmaker,R.H.; Shimon,H.; Baron,M.H. - Absence of prion protein mutation in bipolar manic-depressive patients - British Journal of Psychiatry 1992 Jul; 161: 132
AGRW - Korczyn,A.D.; Chapman,J.C.; Goldfarb,L.G.; Brown,P.; Gajdusek,D.C. - A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin - Annals of the New York Academy of Sciences 1991; 640: 171-6
AHDL - Lee,H.S.; Sambuughin,N.; Cervenakova,L.; Chapman,J.C.; Pocchiari,M.; Litvak,S.; Qi,H.Y.; Budka,H.; del Ser,T.; Furukawa,H.; Brown,P.; Gajdusek,D.C.; Long,J.C.; Korczyn,A.D.; Goldfarb,L.G. - Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease - American Journal of Human Genetics 1999 Apr; 64(4): 1063-70
AKDZ - Rosenmann,H.; Kahana,E.; Korczyn,A.D.; Kahana,I.; Chapman,J.C.; Gabizon,R. - Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob disease - Neurology 1999 Oct 12; 53(6): 1328-9
AKEA - Rosenmann,H.; Vardi,J.; Finkelstein,Y.; Chapman,J.C.; Gabizon,R. - Identification in Israel of 2 Jewish Creutzfeldt-Jakob disease patients with a 178 mutation at their PrP gene - Acta Neurologica Scandinavica 1998 Mar; 97(3): 184-7
AKSR - Shabtai,H.; Nisipeanu,P.; Chapman,J.C.; Korczyn,A.D. - Pruritus in Creutzfeldt-Jakob disease - Neurology 1996 Apr; 46(4): 940-1
AKWV - Simon,E.S.; Kahana,E.; Chapman,J.C.; Treves,T.A.; Gabizon,R.; Rosenmann,H.; Zilber,N.; Korczyn,A.D. - Creutzfeldt-Jakob disease profile in patients homozygous for the PRNP E200K mutation - Annals of Neurology 2000 Feb; 47(2): 257-60
ATFQ - Barron,R.M.; Campbell,S.L.; King,D.; Chapman,K.; Manson,J.C. - Is PrPsc Associated with TSE Infectivity? - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Oral sessions ORAL-21
AOQZ - Campbell,S.L.; Barron,R.M.; Chapman,K.; Manson,J.C. - The Relationship Between PrPsc and Infectivity in Transmissible Spongiform Encephalopathy - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - BR-15
ASGH - Hsiao,K.K.; Nilsen,S.P.; Chapman,P.F. - Abnormal hippocampal synaptic transmission found in transgenic (tg) mice with age-related memory deficits and amyloid plaques - Neurology 1997; 48(N3): 34001
ACMX - Chapman,T.; McKeel,D.W.Jr.; Morris,J.C. - Misleading results with the 14-3-3 assay for the diagnosis of Creutzfeldt-Jakob disease - Neurology 2000 Nov 14; 55(9): 1396-7