ALRR - Tobias,E.; Mann,C.; Bone,I.; de Silva,R.N.; Ironside,J. - A case of Creutzfeldt-Jakob disease presenting with cortical deafness - Journal of Neurology, Neurosurgery and Psychiatry 1994 Jul; 57(7): 872-3
AVLP - Prince,L.A.; Mann,D.; Reilly,T. - Creutzfeldt-Jakob disease: an emergency department presentation of a rare disease. - Journal of Emergency Medicine 2006 Jul; 31(1): 41-4
ACRL - Clinton,J.; Mann,D.M.A.; Roberts,G.W. - Frontal lobe dementia is not a variant of prion disease - Neuroscience Letters 1993 Dec 24; 164(1-2): 1-4
APHG - Fraser,E.; McDonagh,A.M.; Head,M.; Bishop,M.T.; Ironside,J.W.; Mann,D.M.A. - Neuronal and astrocytic responses involving the serotonergic system in human spongiform encephalopathies - Neuropathology and Applied Neurobiology 2003 Oct; 29(5): 482-95
AJLH - Pickering-Brown,S.M.; Mann,D.M.A.; Owen,F.; Ironside,J.W.; de Silva,R.N.; Roberts,D.A.; Balderson,D.J.; Cooper,P.N. - Allelic variations in apolipoprotein E and prion protein genotype related to plaque formation and age of onset in sporadic Creutzfeldt-Jakob disease - Neuroscience Letters 1995 Mar 3; 187(2): 127-9
AKZR - Snowden,J.S.; Mann,D.M.A.; Neary,D. - Distinct neuropsychological characteristics in Creutzfeldt-Jakob disease - Journal of Neurology, Neurosurgery and Psychiatry 2002 Dec; 73(6): 686-94
ALRM - Timperley,W.R.; Mann,D.M.A.; Neary,D.; Davies,S. - Creutzfeldt-Jakob disease: a histochemical study with microdensitometric assay of some enzymes. - Acta Neuropathologica 1973 Nov 5; 26(3): 207-15
AMTH - Wu,C.; Singh,S.K.; Dias,P.; Kumar,S.; Mann,D.M.A. - Activated astrocytes display increased 5-HT2a receptor expression in pathological states - Experimental Neurology 1999 Aug; 158(2): 529-33
AWRK - Bounhar,Y.; Mann,K.K.; Roucou,X.; LeBlanc,A.C. - Prion protein prevents Bax-mediated cell death in the absence of other Bcl-2 family members in Saccharomyces cerevisiae - FEMS Yeast Research 2006 Dec; 6(8): 1204-12
AEAM - Finckh,U.; Müller-Thomsen,T.; Mann,U.; Eggers,C.; Marksteiner,J.; Meins,W.; Binetti,G.; Alberici,A.; Sonderegger,P.; Hock,C.; Nitsch,R.M.; Gal,A. - High frequency of mutations in four different disease genes in early-onset dementia - Annals of the New York Academy of Sciences 2000; 920: 100-6
AEAN - Finckh,U.; Müller-Thomsen,T.; Mann,U.; Eggers,C.; Marksteiner,J.; Meins,W.; Binetti,G.; Alberici,A.; Hock,C.; Nitsch,R.M.; Gal,A. - High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes - American Journal of Human Genetics 2000 Jan; 66(1): 110-7
ARPP - Grasbon-Frodl,E.; Lorenz,H.; Mann,U.; Nitsch,R.M.; Windl,O.; Kretzschmar,H.A. - Loss of glycosylation associated with the T183A mutation in human prion disease - Acta Neuropathologica 2004 Dec; 108(6): 476-84