ABCW - Beaudry,P.; Parchi,P.; Peoc'h,K.; Desbordes,P.; Dartigues,J.F.; Vital,A.; Vital,C.; Capellari,S.; Gambetti,P.; Delasnerie-Laupretre,N.; Mary,J.Y.; Laplanche,J.L. - A French cluster of Creutzfeldt-Jakob disease: a molecular analysis. - European Journal of Neurology 2002 Sep; 9(5): 457-62
AOSI - Faucheux,B.A.; Haik,S.; Sazdovic,V.; Brandel,J.P.; Duyckaerts,C.; Vital,A.; Laplanche,J.L.; Deslys,J.P.; Dormont,D.; Hauw,J.J. - Neuronal loss in the cerebellum of patients with sporadic Creutzfeldt-Jakob disease - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - PG-19
AQJH - Favereaux,A.; Quadrio,I.; Vital,C.; Perret-Liaudet,A.; Anne,O.; Laplanche,J.L.; Petry,K.G.; Vital,A. - Pathologic prion protein spreading in the peripheral nervous system of a patient with sporadic Creutzfeldt-Jakob disease - Archives of Neurology 2004 May; 61(5): 747-50
APXP - Favereaux,A.; Perret-Liaudet,A.; Vital,A. - Extraneural pathologic prion protein - The New England Journal of Medicine 2004 Feb 12; 350(7): 732-3; author reply 732-3
APQQ - Favereaux,A.; Quadrio,I.; Perret-Liaudet,A.; Vital,C.; Ouallet,J.C.; Brochet,B.; Biacabe,A.G.; Petry,K.G.; Kopp,N.; Vital,A. - Prion protein accumulation involving the peripheral nervous system in a sporadic case of Creutzfeldt-Jakob disease - Neuropathology and Applied Neurobiology 2003 Dec; 29(6): 602-5
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
ANRU - Marcaud,V.; Laplanche,J.L.; Defontaines,B.; Beaudry,P.; Vital,A.; Vincent,D.; Sazdovitch,V.; Hauw,J.J.; Latinville,D.; Jung,P.; Vecchierini,F.; Degos,C.F. - [Usefulness of molecular genetic analysis of the PRNP gene in patients with cerebellar ataxia: a new case of fatal familial insomnia] - Interet de l'etude genetique du gene PRNP devant un syndrome cerebelleux: a propos d'un nouveau cas d'insomnie fatale familiale. - Revue Neurologique 2003 Feb; 159(2): 199-202
ATKD - Ugnon-Cafe,S.; Dupin,M.; Esposito,G.; Hoenen,C.; Streichenberger,N.; Vital,A.; Pellissier,J.F.; Moussa,A.; Perron,H.; Perret-Liaudet,A. - Detection of resistant prion protein (PrPres) in human cerebrum by western-blot after streptomycin precipitation - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Diagnosis DIA-15
AYEO - Vital,A.; Canron,M.H.; Gil,R.; Hauw,J.J.; Vital,C. - A sporadic case of Creutzfeldt-Jakob disease with beta-amyloid deposits and alpha-synuclein inclusions - Neuropathology 2007 Jun; 27(3): 273-7
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
ABCW - Beaudry,P.; Parchi,P.; Peoc'h,K.; Desbordes,P.; Dartigues,J.F.; Vital,A.; Vital,C.; Capellari,S.; Gambetti,P.; Delasnerie-Laupretre,N.; Mary,J.Y.; Laplanche,J.L. - A French cluster of Creutzfeldt-Jakob disease: a molecular analysis. - European Journal of Neurology 2002 Sep; 9(5): 457-62
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
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
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
AQJH - Favereaux,A.; Quadrio,I.; Vital,C.; Perret-Liaudet,A.; Anne,O.; Laplanche,J.L.; Petry,K.G.; Vital,A. - Pathologic prion protein spreading in the peripheral nervous system of a patient with sporadic Creutzfeldt-Jakob disease - Archives of Neurology 2004 May; 61(5): 747-50
APQQ - Favereaux,A.; Quadrio,I.; Perret-Liaudet,A.; Vital,C.; Ouallet,J.C.; Brochet,B.; Biacabe,A.G.; Petry,K.G.; Kopp,N.; Vital,A. - Prion protein accumulation involving the peripheral nervous system in a sporadic case of Creutzfeldt-Jakob disease - Neuropathology and Applied Neurobiology 2003 Dec; 29(6): 602-5
AENB - Ghorayeb,I.; Series,C.; Parchi,P.; Sawan,B.; Guez,S.; Laplanche,J.L.; Capellari,S.; Gambetti,P.; Vital,C. - Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case. - Neurology 1998 Jul; 51(1): 271-4
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
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
AHMY - Loiseau,P.; Cohadon,F.; Vital,C.; Coquet,M. - [Creutzfeld-Jakob's disease. Anatomo-clinical study of 2 cases] - La maladie de Creutzfeldt-Jakob. Etude anatomo-clinique de deux observations. - Bordeaux Medical 1972 Nov; 5(18): 2415-23
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
AJHL - Paty,J.; Bonnaud,E.; Latinville,D.; Brenot,P.; Vital,C.; Henry,P.; Faure,J.M. - [A case of Jakob-Creutzfeldt's disease (form of Heidenhain) electrophysiological, clinical and anatomical correlations (author's transl)] - Correlations electrophysiologiques, cliniques et anatomiques dans un cas de maladie de Creutzfeldt-Jakob (forme de Heidenhain) - Revue Neurologique 1978 Mar; 134(3): 223-31
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
AYEO - Vital,A.; Canron,M.H.; Gil,R.; Hauw,J.J.; Vital,C. - A sporadic case of Creutzfeldt-Jakob disease with beta-amyloid deposits and alpha-synuclein inclusions - Neuropathology 2007 Jun; 27(3): 273-7
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
AMXF - Yvonneau,M.; Vital,C.; Belly,C.; Coquet,M. - [Familial syndrome of amyotrophic lateral sclerosis with dementia] - Syndrome familial de sclerose laterale amyotrophique avec demence - Encéphale 1971 Nov-Dec; 60(6): 449-62