Autoren-Indexdatei meiner TSE-Literatur-Datenbank

File of the authors index for my TSE-Literature-Collection

Esmonde,T.F.G.

ACXF - Cousens,S.N.; Zeidler,M.; Esmonde,T.F.G.; de Silva,R.N.; Wilesmith,J.W.; Smith,P.G.; Will,R.G. - Sporadic Creutzfeldt-Jakob disease in the United Kingdom: analysis of epidemiological surveillance data for 1970-96. - British Medical Journal 1997 Aug 16; 315(7105): 389-95

ADCO - de Silva,R.N.; Ironside,J.W.; McCardle,L.; Esmonde,T.F.G.; Bell,J.; Will,R.; Windl,O.; Dempster,M.; Estibeiro,P.; Lathe,R. - Neuropathological phenotype and 'prion protein' genotype correlation in sporadic Creutzfeldt-Jakob disease - Neuroscience Letters 1994 Sep 26; 179(1-2): 50-2

APSD - de Silva,R.N.; Windl,O.; Dempster,M.; Estibeiro,J.P.; Esmonde,T.F.G.; Lathe,R.; Ironside,J.W.; Will,R. - Prion protein genotype in Creutzfeldt-Jakob-disease - the Edinburgh experience - Annals of Neurology 1994; 36(N2): 272-272

ADUT - Esmonde,T.F.G. - Update on Creutzfeldt-Jakob disease - Scottish Medical Journal 1996 Apr; 41(2): 38

ADUU - Esmonde,T.F.G.; Lueck,C.J.; Symon,L.; Duchen,L.W.; Will,R.G. - Creutzfeldt-Jakob disease and lyophilised dura mater grafts: report of two cases. - Journal of Neurology, Neurosurgery and Psychiatry 1993 Sep; 56(9): 999-1000

ADUV - Esmonde,T.F.G.; Will,R.G. - Transmissible spongiform encephalopathies and human neurodegenerative disease - British Journal of Hospital Medicine 1993 Mar 17-Apr 6; 49(6): 400-4, 406

ADUW - Esmonde,T.F.G.; Will,R.G.; Slattery,J.M.; Knight,R.S.G.; Harries-Jones,R.; de Silva,R.N.; Matthews,W.B. - Creutzfeldt-Jakob disease and blood transfusion - Lancet 1993 Jan 23; 341(8839): 205-7

ADUY - Esmonde,T.F.G.; Will,R.G. - Creutzfeldt-Jakob disease in Scotland and Northern Ireland 1980-1989 - Scottish Medical Journal 1992 Dec; 37(6): 181-4

ADUX - Esmonde,T.F.G.; Will,R.G. - Magnetic resonance imaging in Creutzfeldt-Jakob disease - Annals of Neurology 1992 Feb; 31(2): 230-1

AQBG - Hawkins,S.A.C.; Droogan,A.G.; Esmonde,T.F.G.; Allen,I.V.; Will,R.G.; Ironside,J.W. - The first irish case of a newly recognized phenotype of Creutzfeldt-Jakob-disease - Annals of Neurology 1996; 40(N3): T 132-132

AUTY - Heath,C.A.; Barker,R.A.; Esmonde,T.F.G.; Harvey,P.; Roberts,R.; Trend,P.; Head,M.W.; Smith,C.; Bell,J.E.; Ironside,J.W.; Will,R.G.; Knight,R.S.G. - Dura mater-associated Creutzfeldt-Jakob disease: experience from surveillance in the UK. - Journal of Neurology, Neurosurgery and Psychiatry 2006 Jul; 77(7): 880-2

ARLR - Linsell,L.; Cousens,S.N.; Smith,P.G.; Knight,R.S.G.; Zeidler,M.; Stewart,G.; de Silva,R.; Esmonde,T.F.G.; Ward,H.J.T.; Will,R.G. - A case-control study of sporadic Creutzfeldt-Jakob disease in the United Kingdom: analysis of clustering. - Neurology 2004 Dec 14; 63(11): 2077-83

AKLO - Sawcer,S.J.; Yuill,G.M.; Esmonde,T.F.G.; Estibeiro,P.; Ironside,J.W.; Bell,J.E.; Will,R.G. - Creutzfeldt-Jakob disease in an individual occupationally exposed to BSE - Lancet 1993 Mar 6; 341(8845): 642

AMQK - Windl,O.; Dempster,M.; Estibeiro,J.P.; Lathe,R.; de Silva,R.N.; Esmonde,T.F.G.; Will,R.; Springbett,A.; Campbell,T.A.; Sidle,K.C.L.; Palmer,M.S.; Collinge,J. - Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene. - Human Genetics 1996 Sep; 98(3): 259-64

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