ANKT - Andreoletti,O.; Levavasseur,E.; Uro-Coste,E.; Tabouret,G.; Sarradin,P.; Delisle,M.B.; Berthon,P.; Salvayre,R.; Schelcher,F.; Negre-Salvayre,A. - Astrocytes accumulate 4-hydroxynonenal adducts in murine scrapie and human Creutzfeldt-Jakob disease - Neurobiology of Disease 2002 Dec; 11(3): 386-93
AAVG - Atzori,C.; Ghetti,B.; Piva,R.; Srinivasan,A.N.; Zolo,P.; Delisle,M.B.; Mirra,S.S.; Migheli,A. - Activation of the JNK/p38 pathway occurs in diseases characterized by tau protein pathology and is related to tau phosphorylation but not to apoptosis - Journal of Neuropathology and Experimental Neurology 2001 Dec; 60(12): 1190-7
AUGQ - Basset-Leobon,C.; Uro-Coste,E.; Peoc'h,K.; Haik,S.; Sazdovitch,V.; Rigal,M.; Andreoletti,O.; Hauw,J.J.; Delisle,M.B. - Familial Creutzfeldt-Jakob disease with an R208H-129V haplotype and Kuru plaques - Archives of Neurology 2006 Mar; 63(3): 449-52
AXKG - Cassard,H.; Uro-Coste,E.; Simon,S.; Bilheude,J.M.; Perret-Liaudet,A.; Ironside,J.W.; Haik,S.; Basset-Leobon,C.; Lacroux,C.; Peoc'h,K.; Streichenberger,N.; Langeveld,J.P.M.; Head,M.W.; Hauw,J.J.; Schelcher,F.; Delisle,M.B.; Andreoletti,O. - Beyond the PrPres Type1/ Type2 dichotomy in Creutzfeldt-Jakob Disease - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Natural and Experimental Strains P02.15
ARGI - Chretien,F.; Le Pavec,G.; Vallat-Decouvelaere,A.V.; Delisle,M.B.; Uro-Coste,E.; Ironside,J.W.; Gambetti,P.; Parchi,P.; Creminon,C.; Dormont,D.; Mikol,J.; Gray,F.; Gras,G. - Expression of excitatory amino acid transporter-1 (EAAT-1) in brain macrophages and microglia of patients with prion diseases - Journal of Neuropathology and Experimental Neurology 2004 Oct; 63(10): 1058-71
ACVB - Colombier,C.; Geraud,G.; Delisle,M.B.; Laplanche,J.L.; Pavy le Traon,A.; Alize,P.; Delpla,P.A. - [Fatal familial insomnia: phenotypic changes determined by polymorphism of the codon 129] - Insomnie fatale familiale: variation phenotypique determinee par le polymorphisme du codon 129. - Revue Neurologique 1997 May; 153(4): 239-43
ADFP - Delisle,M.B.; Uro-Coste,E.; Gray,F.; Vital,C. - [Fatal familial insomnia] - Insomnie fatale familiale - Clinical and Experimental Pathology 1999; 47(3-4): 176-80
ADFQ - Delisle,M.B.; Fabre,N.; Rochiccioli,P.; Doerr-Schott,J.; Rumeau,J.L.; Bes,A. - [Creutzfeldt-Jakob disease after treatment with human extracted growth hormone. A clinicopathological study] - Maladie de Creutzfeldt-Jakob apres traitement par l'hormone de croissance extractive humaine: etude clinico-pathologique. - Revue Neurologique 1993; 149(10): 524-7
ADNZ - Dorandeu,A.; Wingertsmann,L.; Chretien,F.; Delisle,M.B.; Vital,C.; Parchi,P.; Montagna,P.; Lugaresi,E.; Ironside,J.W.; Budka,H.; Gambetti,P.; Gray,F. - Neuronal apoptosis in fatal familial insomnia - Brain Pathology 1998 Jul; 8(3): 531-7
AEVK - Gray,F.; Adle-Biassette,H.; Chretien,F.; Ereau,T.; Delisle,M.B.; Vital,C. - [Neuronal apoptosis in human prion diseases] - Apoptose neuronale au cours des maladies a prions - Bulletin de l'Académie Nationale de Médecine 1999; 183(2): 305-20; discussion 320-1
AEVL - Gray,F.; Chretien,F.; Adle-Biassette,H.; Dorandeu,A.; Ereau,T.; Delisle,M.B.; Kopp,N.; Ironside,J.W.; Vital,C. - Neuronal apoptosis in Creutzfeldt-Jakob disease - Journal of Neuropathology and Experimental Neurology 1999 Apr; 58(4): 321-8
AQEL - Gray,F.; Delisle,M.B.; Vital,A.; Wingertsmann,L..; Julien,J.; Geraud,G.; Vital,C. - Neuronal apoptosis in human prion diseases - Brain Pathology 1997; 7(N4): 1268
AGCQ - Julien,J.; Vital,C.; Delisle,M.B.; Geraud,G. - The French FFI cases - Brain Pathology 1998 Jul; 8(3): 555-8
AINJ - Montagna,P.; Cortelli,P.; Avoni,P.; Tinuper,P.; Plazzi,G.; Gallassi,R.; Portaluppi,F.; Julien,J.; Vital,C.; Delisle,M.B.; Gambetti,P.; Lugaresi,E. - Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein gene. - Brain Pathology 1998 Jul; 8(3): 515-20