ACES - Capellari,S.; Vital,C.; Parchi,P.; Petersen,R.B.; Ferrer,X.; Jarnier,D.; Pegoraro,E.; Gambetti,P.; Julien,J. - Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family - Neurology 1997 Jul; 49(1): 133-41
APNO - Capellari,S.; Parchi,P.; Landis,D.D.; Julien,J.; Vital,C.; Dickson,D.D.; Richardson,S.L.; Petersen,R.B.; Gambetti,P. - Prion encephalopathy with octapeptide repeats insertion - a study of 3 families - Neurology 1997; 48(N3): 5035
ACNV - Chen,S.G.; Parchi,P.; Brown,P.; Capellari,S.; Zou,W.Q.; Cochran,E.J.; Vnencak-Jones,C.L.; Julien,J.; Vital,C.; Mikol,J.; Lugaresi,E.; Autilio-Gambetti,L.; Gambetti,P. - Allelic origin of the abnormal prion protein isoform in familial prion diseases - Nature Medicine 1997 Sep; 3(9): 1009-15
AEQY - Goldfarb,L.G.; Petersen,R.B.; Tabaton,M.; Brown,P.; LeBlanc,A.C.; Montagna,P.; Cortelli,P.; Julien,J.; Vital,C.; Pendelbury,W.W.; Haltia,M.; Willis,P.R.; Hauw,J.J.; McKeever,P.E.; Monari,L.; Schrank,B.; Swergold,G.D.; Autilio-Gambetti,L.; Gajdusek,D.C.; Lugaresi,E.; Gambetti,P. - Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. - Science 1992 Oct 30; 258(5083): 806-8
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
AJET - Parchi,P.; Giese,A.; Capellari,S.; Brown,P.; Schulz-Schaeffer,W.J.; Windl,O.; Zerr,I.; Budka,H.; Kopp,N.; Piccardo,P.; Poser,S.; Rojiani,A.; Streichenberger,N.; Julien,J.; Vital,C.; Ghetti,B.; Gambetti,P.; Kretzschmar,H.A. - Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects - Annals of Neurology 1999 Aug; 46(2): 224-33
AJKI - Petersen,R.B.; Tabaton,M.; Berg,L.; Schrank,B.; Torack,R.M.; Leal,S.; Julien,J.; Vital,C.; Deleplanque,B.; Pendlebury,W.W.; et al. - Analysis of the prion protein gene in thalamic dementia - Neurology 1992 Oct; 42(10): 1859-63
AMBG - Vital,C.; Gray,F.; Vital,A.; Ferrer,X.; Julien,J. - Prion disease with octapeptide repeat insertion - Clinical and Experimental Pathology 1999; 47(3-4): 153-9
AMBH - Vital,C.; Gray,F.; Vital,A.; Parchi,P.; Capellari,S.; Petersen,R.B.; Ferrer,X.; Jarnier,D.; Julien,J.; Gambetti,P. - Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits. - Neuropathology and Applied Neurobiology 1998 Apr; 24(2): 125-30
ARXB - Vital,C.; Gray,F.; Vital,A.; Parchi,P.; Capellari,S.; Petersen,R.B.; Julien,J.; Gambetti,P. - Cerebellar modifications at immunohistochemical study (IHC) in 3 cases of prion encephalopathy with octapeptide repeat insertion (OPRI) - Journal of Neuropathology and Experimental Neurology 1997; 56(N5): 591 Nr. 79
AXPL - Julien,O.; Sykes,B.D. - Investigation of Prions Structure and Stability by NMR - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Protein Misfolding P01.74
ARNQ - Barret,A.; Forestier,L.; Deslys,J.P.; Julien,R.; Gallet,P.F. - Glycosylation-related gene expression in prion diseases: PrPsc accumulation in scrapie infected GT1 cells depends on beta-1,4-linked GalNAc-4-SO4 hyposulfation. - The Journal of Biological Chemistry 2005 Mar 18; 280(11): 10516-23
AOPZ - Barret,A.; Gallet,P.F.; Simoneau,S.; Forestier,L.; Jayat-Vignolles,C.; Larramendy,C.; Papy-Garcia,D.; Barritault,D.; Julien,R.; Deslys,J.P. - Glycogenome expression changes in prion infected cells and after treatment by heparan mimetics - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - BR-100