ABTL - Brown,J.; Gydesen,S.; Sorensen,S.A.; Brun,A.; Smith,S.; Houlden,H.; Twells,R.; Mullan,M.; Rossor,M.; Collinge,J.; Palmer,M.; Goate,A.; Hardy,J. - Genetic characterization of a familial non-specific dementia originating in Jutland, Denmark - Journal of the Neurological Sciences 1993 Feb; 114(2): 138-43
ABTM - Brown,J.; Smith,S.; Brun,A.; Collinge,J.; Gydesen,S.; Hardy,J.; Mullan,M.; Goate,A. - Genetic characterization of a novel familial dementia - Annals of the New York Academy of Sciences 1991; 640: 181-3
ACRN - Clinton,J.; Lantos,P.L.; Rossor,M.; Mullan,M.; Roberts,G.W. - Immunocytochemical confirmation of prion protein - Lancet 1990 Aug 25; 336(8713): 515
ACUG - Collinge,J.; Brown,J.; Hardy,J.; Mullan,M.; Rossor,M.N.; Baker,H.F.; Crow,T.J.; Lofthouse,R.; Poulter,M.; Ridley,R.; Owen,F.; Bennett,C.; Dunn,G.; Harding,A.E.; Quinn,N.; Doshi,B.; Roberts,G.W.; Honavar,M.; Janota,I.; Lantos,P.L. - Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features. - Brain: A Journal of Neurology 1992 Jun; 115(3): 687-710
ACUJ - Collinge,J.; Owen,F.; Poulter,M.; Leach,M.; Crow,T.J.; Rossor,M.N.; Hardy,J.; Mullan,M.J.; Janota,I.; Lantos,P.L. - Prion dementia without characteristic pathology - Lancet 1990 Jul 7; 336(8706): 7-9
AJOM - Poulter,M.; Baker,H.F.; Frith,C.D.; Leach,M.; Lofthouse,R.; Ridley,R.M.; Shah,T.; Owen,F.; Collinge,J.; Brown,J.; Hardy,J.; Mullan,M.J.; Harding,A.E.; Bennett,C.; Doshi,R.; Crow,T.J. - Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies. - Brain: A Journal of Neurology 1992 Jun; 115(3): 675-85