AAGR - Amouyel,P.; Alperovitch,A.; Delasnerie-Laupretre,N.; Laplanche,J.L. - Apolipoprotein E in Creutzfeldt-Jakob disease. French Research Group on Epidemiology of Human Spongiform Encephalopathies. - Lancet 1995 Mar 4; 345(8949): 595-6
AAGS - Amouyel,P.; Vidal,O.; Launay,J.M.; Laplanche,J.L. - The apolipoprotein E alleles as major susceptibility factors for Creutzfeldt-Jakob disease. The French Research Group on Epidemiology of Human Spongiform Encephalopathies. - Lancet 1994 Nov 12; 344(8933): 1315-8
AASE - Antoine,J.C.; Michel,D.; Bertholon,P.; Mosnier,J.F.; Laplanche,J.L.; Beaudry,P.; Hauw,J.J.; Veyret,C. - Creutzfeldt-Jakob disease after extracranial dura mater embolization for a nasopharyngeal angiofibroma - Neurology 1997 May; 48(5): 1451-3
AASF - Antoine,J.C.; Laplanche,J.L.; Mosnier,J.F.; Beaudry,P.; Chatelain,J.C.; Michel,D. - Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein gene - Neurology 1996 Apr; 46(4): 1123-7
AOPT - Arlotto,M.; Peoc'h,K.; Cazorla,M.; Hayer,M.; Windl,O.; Laplanche,J.L.; Lehmann,S. - Proteomic research of TSEs - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-27
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
ABCX - Beaudry,P.; Cohen,P.; Brandel,J.P.; Delasnerie-Laupretre,N.; Richard,S.; Launay,J.M.; Laplanche,J.L. - 14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease - Dementia and Geriatric Cognitive Disorders 1999 Jan-Feb; 10(1): 40-6
ABCY - Beaugerie,L.; Andre,C.; Laplanche,J.L. - Search for asymptomatic coeliac disease in patients with spongiform encephalopathy - Gastroenterologie Clinique et Biologique 1999 Mar; 23(3): 411-2
APUA - Biacabe,A.G.; Laplanche,J.L.; Ryder,S.; Baron,T.G.M. - Distinct molecular phenotypes in bovine prion diseases - EMBO Reports 2004 Jan; 5(1): 110-5
AOQJ - Biacabe,A.G.; Laplanche,J.L.; Ryder,S.; Baron,T.G.M. - A Molecular Variant of Bovine Spongiform Encephalopatie - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Oral sessions OS-30
ATND - Brandel,J.P.; Haik,S.; Delasnerie-Laupretre,N.; Le Masson,V.; Salomon,D.; Laplanche,J.L.; Hauw,J.J.; Alperovitch,A. - Variant Creutzfeldt-Jakob in France - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Human prions, risk of blood products, and therapy HUMAN-01
AOFD - Brandel,J.P.; Preece,M.; Brown,P.; Croes,E.A.; Laplanche,J.L.; Agid,Y.; Will,R.; Alperovitch,A. - Distribution of codon 129 genotype in human growth hormone-treated CJD patients in France and the UK - Lancet 2003 Jul 12; 362(9378): 128-30
ABPN - Brandel,J.P.; Peoc'h,K.; Beaudry,P.; Welaratne,A.; Bottos,C.; Agid,Y.; Laplanche,J.L. - 14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients - Annals of Neurology 2001 Feb; 49(2): 257-60
ABPO - Brandel,J.P.; Delasnerie-Laupretre,N.; Laplanche,J.L.; Hauw,J.J.; Alperovitch,A. - Diagnosis of Creutzfeldt-Jakob disease: Effect of clinical criteria on incidence estimates. - Neurology 2000 Mar 14; 54(5): 1095-9
ABPP - Brandel,J.P.; Beaudry,P.; Delasnerie-Laupretre,N.; Laplanche,J.L. - [Creutzfeldt-Jakob disease: diagnostic value of protein 14-3-3 and neuronal specific enolase assay in cerebrospinal fluid] - Maladie de Creutzfeldt-Jakob: valeur diagnostique de la detection de la proteine 14-3-3 et du dosage de la NSE dans le liquide cephalo-rachidien. - Revue Neurologique 1999 Feb; 155(2): 148-51
ABPT - Brandel,J.P.; Delasnerie-Laupretre,N.; Laplanche,J.L.; Dormont,D.; Hauw,J.J.; Alperovitch,A. - [A study network of human spongiform encephalopathies: 1st results] - Reseau d'etudes des encephalopathies spongiformes humaines: premiers resultats. - Revue Neurologique 1994 Oct; 150(10): 684-8
ABYG - Brugere-Picoux,J.; Chatelain,J.C.; Laplanche,J.L.; Brugere,H. - [Transmissible animal spongiform encephalopathies] - Les encephalopathies spongiformes transmissibles animales - Bulletin de l'Académie Nationale de Médecine 1994 May; 178(5): 873-83; discussion 883-5
ACEN - Caparros-Lefebvre,D.; Sazdovitch,V.; Roudier,M.; Brandel,J.P.; Laplanche,J.L.; Deslys,J.P.; Hauw,J.J. - Creutzfeldt-Jakob disease in French West Indies - Lancet 1999 May 1; 353(9163): 1495-6
AVSE - Chasseigneaux,S.; Haik,S.; Laffont-Proust,I.; De Marco,O.; Lenne,M.; Brandel,J.P.; Hauw,J.J.; Laplanche,J.L.; Peoc'h,K. - V180I mutation of the prion protein gene associated with atypical PrPsc glycosylation - Neuroscience Letters 2006 Nov 20; 408(3): 165-9
ATPT - Chasseigneaux,S.; Peoc'h,K.; Haik,S.; De Marco,O.; Launay,J.M.; Lenne,M.; Brandel,J.P.; Laplanche,J.L. - V180I mutation of the prion gene associated to atypical PrPsc glycosylation - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Pathogenesis PATH-30
AYEY - Chatelain,J.C.; Brugere-Picoux,J.; Laplanche,J.L. - Les encephalopathies spongiformes subaigues (ou tremblantes) des ruminants - Recueil de Médecine Vétérinaire 1990; 166(12): 1103-10
ACNP - Chebassier,C.; Mouillet-Richard,S.; Laplanche,J.L.; Kellermann,O.; Launay,J.M. - [A signaling function for the prion protein] - Une fonction de signalisation pour la proteine prion - Pathologie Biologie 2001 Apr; 49(3): 191-3
ACRO - Clouscard,C.; Beaudry,P.; Elsen,J.M.; Milan,D.; Dussaucy,M.; Bounneau,C.; Schelcher,F.; Chatelain,J.C.; Launay,J.M.; Laplanche,J.L. - Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapie - Journal of General Virology 1995 Aug; 76(8): 2097-101
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
AQXT - Comincini,S.; Facoetti,A.; Del Vecchio,I.; Peoc'h,K.; Laplanche,J.L.; Magrassi,L.; Ceroni,M.; Ferretti,L.; Nano,R. - Differential expression of the prion-like protein doppel gene (PRND) in astrocytomas: a new molecular marker potentially involved in tumor progression. - Anticancer Research 2004 May-Jun; 24(3a): 1507-17
ASTF - Dauvilliers,Y.; Cervena,K.; Carlander,B.; Espa,F.; Bassetti,C.L.; Claustrat,B.; Laplanche,J.L.; Billiard,M.; Touchon,J. - Dissociation in circadian rhythms in a pseudohypersomnia form of fatal familial insomnia - Neurology 2004 Dec 28; 63(12): 2416-8
ADCK - de Seze,J.; Hache,J.C.; Vermersch,P.; Arndt,C.F.; Maurage,C.A.; Pasquier,F.; Laplanche,J.L.; Ruchoux,M.M.; Leys,D.; Destee,A.; Petit,H. - Creutzfeldt-Jakob disease: neurophysiologic visual impairments. - Neurology 1998 Oct; 51(4): 962-7
AUYD - Dimitri,D.; Jehel,L.; Durr,A.; Levy-Soussan,M.; Andreux,V.; Laplanche,J.L.; Fossati,P.; Cohen,D. - Fatal familial insomnia presenting as psychosis in an 18-year-old man - Neurology 2006 Jul 25; 67(2): 363-4
ADPR - Dreux,C.; Launay,J.M.; Laplanche,J.L. - [Recent data on prion diseases] - Donnees recentes sur les maladies a prions - Bulletin et Memoires de l'Academie Royale de Medecine de Belgique 2000; 155(1-2): 99-108; discussion 108-11
ADPS - Dreux,C.; Laplanche,J.L.; Chatelain,J.C. - [Human transmissible dementia: prion diseases?] - Les demences transmissibles humaines: maladies a prions? - Bulletin de l'Académie Nationale de Médecine 1992 Nov; 176(8): 1279-88; discussion 1289-91
ADTM - Elsen,J.M.; Amigues,Y.; Schelcher,F.; Ducrocq,V.; Andreoletti,O.; Eychenne,F.; Khang,J.V.T.; Poivey,J.P.; Lantier,F.; Laplanche,J.L. - Genetic susceptibility and transmission factors in scrapie: detailed analysis of an epidemic in a closed flock of Romanov. - Archives of Virology 1999; 144(3): 431-45
ADUC - Erginel-Unaltuna,N.; Peoc'h,K.; Komurcu,E.; Acuner,T.T.; Issever,H.; Laplanche,J.L. - Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease - European Journal of Human Genetics 2001 Dec; 9(12): 965-8
AXMB - Faucheux,B.A.; Privat,N.; Sazdovitch,V.; Brandel,J.P.; Matos,A.; Maurage,C.A.; Laplanche,J.L.; Deslys,J.P.; Hauw,J.J.; Haik,S. - Neuronal Loss and Prion Protein (PrP) Depositon in Sporadic Creutzfeldt-Jakob Disease - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Pathology and Pathogenesis P03.07
ATPB - Faucheux,B.A.; Privat,N.; Laffont-Proust,I.; Sazdovitch,V.; Matos,A.; Brandel,J.P.; Maurage,C.A.; Laplanche,J.L.; Hauw,J.J.; Haik,S. - Is microglial activation significantly correlated to PrPres deposits and neuronal loss in the brain of patients with sporadic Creutzfeldt-Jakob disease? - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Pathogenesis PATH-12
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
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
AEOK - Gidon-Jeangirard,C.; Hugel,B.; Holl,V.; Toti,F.; Laplanche,J.L.; Meyer,D.; Freyssinet,J.M. - Annexin V delays apoptosis while exerting an external constraint preventing the release of CD4+ and PrPc+ membrane particles in a human T lymphocyte model - Journal of Immunology 1999 May 15; 162(10): 5712-8
AEPI - Giraud,P.; Perret-Liaudet,A.; Biacabe,A.G.; Deslys,J.P.; Laplanche,J.L.; Chazot,G.; Kop,N. - [Non-familial Creutzfeldt-Jakob disease: a study of 53 cases] - Maladie de Creutzfeldt-Jakob non familiale certaine: etude de 53 observations. - Revue Neurologique 2000 Jul; 156(6-7): 616-21
AEVM - Gray,F.; Chretien,F.; Cesaro,P.; Chatelain,J.C.; Beaudry,P.; Laplanche,J.L.; Mikol,J.; Bell,J.; Gambetti,P.; Degos,J.D. - Creutzfeldt-Jakob disease and cerebral amyloid angiopathy - Acta Neuropathologica 1994 Jul; 88(1): 106-11
ASTO - Haik,S.; Brandel,J.P.; Salomon,D.; Sazdovitch,V.; Delasnerie-Laupretre,N.; Laplanche,J.L.; Faucheux,B.A.; Soubrie,C.; Boher,E.; Belorgey,C.; Hauw,J.J.; Alperovitch,A. - Compassionate use of quinacrine in Creutzfeldt-Jakob disease fails to show significant effects - Neurology 2004 Dec 28; 63(12): 2413-5
ARHO - Haik,S.; Peoc'h,K.; Brandel,J.P.; Privat,N.; Laplanche,J.L.; Faucheux,B.A.; Hauw,J.J. - Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation - Annals of Neurology 2004 Dec; 56(6): 909-10; author reply 910-1
AOTS - Haik,S.; Brandel,J.P.; Salomon,D.; Sazdovitch,V.; Delasnerie-Laupretre,N.; Fierville,F.; Laplanche,J.L.; Faucheux,B.A.; Hauw,J.J.; Alperovitch,A. - Clinical and neuropathological features of CJD patients treated with Quinacrine in France - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - IV-26
AFAJ - Haik,S.; Brandel,J.P.; Sazdovitch,V.; Delasnerie-Laupretre,N.; Peoc'h,K.; Laplanche,J.L.; Privat,N.; Duyckaerts,C.; Kemeny,J.L.; Kopp,N.; Laquerriere,A.; Mohr,M.; Deslys,J.P.; Dormont,D.; Hauw,J.J. - Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease - Neurology 2000 Nov 14; 55(9): 1401-4
AFFN - Hauw,J.J.; Sazdovitch,V.; Laplanche,J.L.; Peoc'h,K.; Kopp,N.; Kemeny,J.; Privat,N.; Delasnerie-Laupretre,N.; Brandel,J.P.; Deslys,J.P.; Dormont,D.; Alperovitch,A. - Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene - Neurology 2000 Apr 25; 54(8): 1641-6
ACZP - Huillard d'Aignaux,J.N.; Cousens,S.N.; Delasnerie-Laupretre,N.; Brandel,J.P.; Salomon,D.; Laplanche,J.L.; Hauw,J.J.; Alperovitch,A. - Analysis of the geographical distribution of sporadic Creutzfeldt-Jakob disease in France between 1992 and 1998 - International Journal of Epidemiology 2002 Apr; 31(2): 490-5
ACZQ - Huillard d'Aignaux,J.N.; Laplanche,J.L.; Delasnerie-Laupretre,N.; Brandel,J.P.; Peoc'h,K.; Salomon,D.; Hauw,J.J.; Alperovitch,A. - Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7 - Journal of Neurology, Neurosurgery and Psychiatry 2000 Jun; 68(6): 787-9
AGRL - Kopp,N.; Streichenberger,N.; Deslys,J.P.; Laplanche,J.L.; Chazot,G. - Creutzfeldt-Jakob disease in a 52-year-old woman with florid plaques - Lancet 1996 Nov 2; 348(9036): 1239-40
AUKZ - Kopp,N.; Streichenberger,N.; Philippeau,F.; Gros,E.; Laplanche,J.L.; Chazot,G. - The new variant of Creutzfeldt-Jakob-disease - Point Veterinaire 1996; 28(179): 43-8
AGYN - Labauge,P.; Pages,M.; Blard,J.M.; Chatelain,J.C.; Laplanche,J.L. - Valine homozygous 129 PrP genotype in a French growth-hormone-related Creutzfeldt-Jakob disease patient - Neurology 1993 Feb; 43(2): 447
ANMF - Laplanche,J.L.; Lepage,V.; Peoc'h,K.; Delasnerie-Laupretre,N.; Charron,D. - HLA in French patients with variant Creutzfeldt-Jakob disease - Lancet 2003 Feb 8; 361(9356): 531-2
AHAN - Laplanche,J.L.; Hachimi,K.H.; Durieux,I.; Thuillet,P.; Defebvre,L.; Delasnerie-Laupretre,N.; Peoc'h,K.; Foncin,J.F.; Destee,A. - Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene - Brain: A Journal of Neurology 1999 Dec; 122(12): 2375-86
AHAO - Laplanche,J.L. - [Unconventional transmissible agents and prion protein: is something still missing?] - Agents transmissibles non conventionnels et proteine prion: manque-t-il encore quelque chose? - Annales de Biologie Clinique 1997 Sep-Oct; 55(5): 395-407
ASCE - Laplanche,J.L. - Molecular-genetics of familial and sporadic forms of human prion diseases - Medecine et Maladies Infectieuses 1996; 26(NBIS): 264-70
AHAP - Laplanche,J.L.; Delasnerie-Laupretre,N.; Brandel,J.P.; Dussaucy,M.; Chatelain,J.C.; Launay,J.M. - Two novel insertions in the prion protein gene in patients with late-onset dementia - Human Molecular Genetics 1995 Jun; 4(6): 1109-11
AHAQ - Laplanche,J.L.; Beaudry,P.; Ripoll,L.; Launay,J.M. - [Prion protein: structure, functions and polymorphisms associated with human spongiform encephalopathies] - Proteine prion: structure, fonctions et polymorphismes associes aux encephalopathies spongiformes humaines. - Pathologie Biologie 1995 Feb; 43(2): 104-13
AHAR - Laplanche,J.L.; Launay,J.M.; Dreux,C. - [Molecular genetics of familial and sporadic forms of human prion diseases] - Genetique moleculaire des formes familiales et sporadiques des maladies a prions humaines - Annales Pharmaceutiques Francaises 1995; 53(5): 193-200
AHAS - Laplanche,J.L.; Delasnerie-Laupretre,N.; Brandel,J.P.; Chatelain,J.C.; Beaudry,P.; Alperovitch,A.; Launay,J.M. - Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies. - Neurology 1994 Dec; 44(12): 2347-51
AHAT - Laplanche,J.L. - [Molecular basis of familial and sporadic forms of human prion diseases] - Bases moleculaires des formes familiales et sporadiques des maladies a prions humaines - Transfusion Clinique et Biologique 1994; 1(5): 345-53
AHAU - Laplanche,J.L.; Chatelain,J.C.; Dussaucy,M.; Bounneau,C.; Launay,J.M.; Brandel,J.P.; Delasnerie-Laupretre,N. - Inherited prion disease - British Medical Journal 1993 Mar 20; 306(6880): 794-5
AHAV - Laplanche,J.L.; Chatelain,J.C.; Beaudry,P.; Dussaucy,M.; Bounneau,C.; Launay,J.M. - French autochthonous scrapied sheep without the 136Val PrP polymorphism - Mammalian Genome 1993; 4(8): 463-4
AHAW - Laplanche,J.L.; Chatelain,J.C.; Westaway,D.; Thomas,S.; Dussaucy,M.; Brugere-Picoux,J.; Launay,J.M. - PrP polymorphisms associated with natural scrapie discovered by denaturing gradient gel electrophoresis - Genomics 1993 Jan; 15(1): 30-7
AHAX - Laplanche,J.L.; Chatelain,J.C.; Thomas,S.; Launay,J.M.; Gaultier,C.; Derouesne,C. - Uncommon phenotype for a codon 178 mutation of the human PrP gene - Annals of Neurology 1992 Mar; 31(3): 345
ASCF - Laplanche,J.L.; Chatelain,J.C.; Thomas,S.; Dussaucy,M.; Brugere-Picoux,J.; Launay,J.M. - Prp gene allelic variants and natural scrapie in French Ile-de-France and Romanov sheep - "Prions diseases in humans and animals", Ed. S. Prusiner et coll, Ed.Ell's Horwood, New-York 1992, p 329-33
AHAY - Laplanche,J.L.; Chatelain,J.C.; Thomas,S.; Brown,P.; Cathala,F. - [Analysis of the PrP gene in a Tunisian family with Creutzfeldt-Jakob disease] - Analyse du gene PrP dans une famille d'origine tunisienne atteinte de maladie de Creutzfeldt-Jakob - Revue Neurologique 1991; 147(12): 825-7
AHAZ - Laplanche,J.L.; Chatelain,J.C.; Launay,J.M.; Gazengel,C.; Vidaud,M. - Deletion in prion protein gene in a Moroccan family - Nucleic Acids Research 1990 Nov 25; 18(22): 6745
AHFJ - Leuck,J.; Peoch,K.; Laplanche,J.L.; Grabar,E.; Müller,W.E.G.; Schröder,H.C. - A novel binding assay for detection of 14-3-3 protein in cerebrospinal fluid from Creutzfeldt-Jakob patients - Cellular and Molecular Biology (Noisy-le-Grand, France) 2000 Nov; 46(7): 1291-6
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
ATMU - Michaud,D.; Privat,N.; Laffont-Proust,I.; Sazdovitch,V.; Peoc'h,K.; Laplanche,J.L.; Faucheux,B.A.; Hauw,J.J.; Haik,S. - PrPsc deposit in ten different prion diseases : an immmunihistochemical study using a panel of monoclonal antibodies - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Genetics, strains and emerging problems GEN-20
AIPR - Mouillet-Richard,S.; Ermonval,M.; Chebassier,C.; Laplanche,J.L.; Lehmann,S.; Launay,J.M.; Kellermann,O. - Signal transduction through prion protein - Science 2000 Sep 15; 289(5486): 1925-8
AIPS - Mouillet-Richard,S.; Laurendeau,I.; Vidaud,M.; Kellermann,O.; Laplanche,J.L. - Prion protein and neuronal differentiation: quantitative analysis of prnp gene expression in a murine inducible neuroectodermal progenitor. - Microbes and Infection 1999 Oct; 1(12): 969-76
AIPT - Mouillet-Richard,S.; Teil,C.; Lenne,M.; Hugon,S.; Taleb,O.; Laplanche,J.L. - Mutation at codon 210 (V210I) of the prion protein gene in a North African patient with Creutzfeldt-Jakob disease - Journal of the Neurological Sciences 1999 Oct 15; 168(2): 141-4
AIQJ - Müller,W.E.G.; Laplanche,J.L.; Ushijima,H.; Schröder,H.C. - Novel approaches in diagnosis and therapy of Creutzfeldt-Jakob disease - Mechanisms of Ageing and Development 2000 Jul 31; 116(2-3): 193-218
AJDV - Palmer,M.S.; Mahal,S.P.; Campbell,T.A.; Hill,A.F.; Sidle,K.C.L.; Laplanche,J.L.; Collinge,J. - Deletions in the prion protein gene are not associated with CJD - Human Molecular Genetics 1993 May; 2(5): 541-4
AJFO - Parodi,A.L.; Brugere-Picoux,J.; Chatelain,J.C.; Laplanche,J.L. - [Bovine spongiform encephalopathy: a new entity caused by a non-conventional transmissible agent] - L'encephalopathie spongiforme bovine: une nouvelle entite provoquee par un agent transmissible non conventionnel. - Bulletin de l'Académie Nationale de Médecine 1990 Jun-Jul; 174(6): 731-9; discussion 740-1
ATHQ - Pastore,M.; Chasseigneaux,S.; Britton-Davidian,J.; Catalan,J.; Steverlynck,C.; Casanova,D.; Laplanche,J.L.; Bürkle,A.; Lehmann,S.L. - Investigation on the biological basis of prion susceptibility and resistance in N2A neuroblastoma subclones - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Cell Biology of PrPc and PrPsc CELL-22
AXUH - Peoc'h,K.; Brandel,J.P.; Chasseigneaux,S.; Leandre,S.; Laplanche,J.L. - Polymorphism at Codon 129 of PRNP in a Population of Patients Initially Suspected of Creuzfeldt-Jakob Disease - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Pathology and Pathogenesis P03.152
AUOH - Peoc'h,K.; Delasnerie-Laupretre,N.; Beaudry,P.; Laplanche,J.L. - Diagnostic value of CSF 14-3-3 detection in sporadic CJD diagnosis according to the age of the patient - European Journal of Neurology 2006 Apr; 13(4): 427-8
AOXU - Peoc'h,K.; Frobert,Y.; Volland,H.; Boquet,D.; Sato,T.A.; Clement,G.; Grassi,J.; Laplanche,J.L.; Creminon,C. - Production of monoclonal antibodies against 14-3-3 protein and their use for CJD diagnosis - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-40
ANKY - Peoc'h,K.; Volland,H.; de Gassart,A.; Beaudry,P.; Sazdovitch,V.; Sorgato,M.C.; Creminon,C.; Laplanche,J.L.; Lehmann,S. - Prion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt-Jakob disease - FEBS Letters 2003 Feb 11; 536(1-3): 61-5
AJIL - Peoc'h,K.; Serres,C.; Frobert,Y.; Martin,C.; Lehmann,S.; Chasseigneaux,S.; Sazdovitch,V.; Grassi,J.; Jouannet,P.; Launay,J.M.; Laplanche,J.L. - The human "prion-like" protein Doppel is expressed in both Sertoli cells and spermatozoa - The Journal of Biological Chemistry 2002 Nov 8; 277(45): 43071-8
AJIM - Peoc'h,K.; Beaudry,P.; Laupretre,N.; Laplanche,J.L. - CSF detection of the 14-3-3 protein in unselected patients with dementia - Neurology 2002 Feb 12; 58(3): 509-10
AJIN - Peoc'h,K.; Schröder,H.C.; Laplanche,J.L.; Ramljak,S.; Müller,W.E.G. - Determination of 14-3-3 protein levels in cerebrospinal fluid from Creutzfeldt-Jakob patients by a highly sensitive capture assay - Neuroscience Letters 2001 Apr 6; 301(3): 167-70
AJIO - Peoc'h,K.; Guerin,C.; Brandel,J.P.; Launay,J.M.; Laplanche,J.L. - First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases. - Neuroscience Letters 2000 Jun 2; 286(2): 144-8
AJIP - Peoc'h,K.; Manivet,P.; Beaudry,P.; Attane,F.; Besson,G.; Hannequin,D.; Delasnerie-Laupretre,N.; Laplanche,J.L. - Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype - Human Mutation 2000 May; 15(5): 482
AJIQ - Peoc'h,K.; Laplanche,J.L. - [Genetics of human subacute spongiform encephalopathies] - Genetique des encephalopathies spongiformes subaigues humaines - Revue du Praticien 1999 May 1; 49(9): 954-8
ANYY - Plamont,M.A.; Chasseigneaux,S.; Delasnerie-Laupretre,N.; Beaudry,P.; Peoc'h,K.; Laplanche,J.L. - Variation at the ADAM10 gene locus is not associated with Creutzfeldt-Jakob disease - Neuroscience Letters 2003 Jun 26; 344(2): 132-4
AXUW - Privat,N.; Laffont-Proust,I.; Faucheux,B.A.; Sazdovitch,V.; Frobert,Y.; Laplanche,J.L.; Grassi,J.; Hauw,J.J.; Haik,S. - PrP Immunohistochemistry in Human Prion Diseases: from Antibody Screening to a Standardized fast Immunodiagnosis using Automation - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Pathology and Pathogenesis P03.36
AJPU - Privat,N.; Sazdovitch,V.; Seilhean,D.; Laplanche,J.L.; Hauw,J.J. - PrP immunohistochemistry: different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for deposits in sporadic Creutzfeldt-Jakob disease. - Microscopy Research and Technique 2000 Jul 1; 50(1): 26-31
AKAP - Ripoll,L.; Laplanche,J.L.; Salzmann,M.; Jouvet,A.; Planques,B.; Dussaucy,M.; Chatelain,J.C.; Beaudry,P.; Launay,J.M. - A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease - Neurology 1993 Oct; 43(10): 1934-8
ATWB - Rodriguez,M.M.; Peoc'h,K.; Haik,S.; Bouchet,C.; Vernengo,L.; Manana,G.; Salamano,R.; Carrasco,L.; Lenne,M.; Beaudry,P.; Launay,J.M.; Laplanche,J.L. - A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease - Neurology 2005 Apr 26; 64(8): 1455-7
AKGD - Ruffie,A.; Delasnerie-Laupretre,N.; Brandel,J.P.; Jaussent,I.; Dormont,D.; Laplanche,J.L.; Hauw,J.J.; Richardson,S.; Alperovitch,A. - [Incidence of Creutzfeldt-Jakob disease in France, 1992-1995] - Incidence de la maladie de Creutzfeldt-Jakob en France, 1992-1995 - Revue d'Épidémiologie et de Santé Publique 1997 Dec; 45(6): 448-53
AVEM - Serres,C.; Peoc'h,K.; Courtot,A.M.; Lesaffre,C.; Jouannet,P.; Laplanche,J.L. - Spatio-developmental distribution of the prion-like protein doppel in Mammalian testis: a comparative analysis focusing on its presence in the acrosome of spermatids. - Biology of Reproduction 2006 May; 74(5): 816-23
ARVW - Silverman,G.L.; Yao,H.; Strome,R.; Laplanche,J.L.; Foncin,J.F.; George-Hyslop,P.St; Fraser,P.E.; Westaway,D. - Proteins which interact with wild-type and mutant N-terminal domains of human PrPc - Journal of Neuropathology and Experimental Neurology 1997; 56(N5): 596 Nr. 99
AOZF - Sitzmann,L.; Brandel,J.P.; Delasnerie-Laupretre,N.; Laplanche,J.L.; Perret-Liaudet,A.; Fleury,H.; Alperovitch,A. - Could a Modification of Inclusion Criteria Lead to an Earlier Treatment of Patients With Sporadic CJD ? - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-49
ALFF - Streichenberger,N.; Biacabe,A.G.; Perret-Liaudet,A.; Deslys,J.P.; Laplanche,J.L.; Chazot,G.; Kopp,N. - This is really a case of new variant Creutzfeldt-Jakob. Response to C.J.G. Lang et al. concerning our article Acta Neuropathol (2000) 99:704-708. - Acta Neuropathologica 2001 Dec; 102(6): 647-8
ALFG - Streichenberger,N.; Jordan,D.; Verejan,I.; Souchier,C.; Philippeau,F.; Gros,E.; Mottolese,C.; Ostrowsky,K.; Perret-Liaudet,A.; Laplanche,J.L.; Hermier,M.; Deslys,J.P.; Chazot,G.; Kopp,N. - The first case of new variant Creutzfeldt-Jakob disease in France: clinical data and neuropathological findings. - Acta Neuropathologica 2000 Jun; 99(6): 704-8
AWOY - Tiers,L.; Peoc'h,K.; Roche,S.; Laplanche,J.L.; Lehmann,S. - In search for blood TSE biomarkers using the SELDI (surface-enhanced laser desorption/ionization) approach - International Conference - Prion 2006: Strategies, advances and trends towards protection of society - 3.10.-6.10.2006, Torino, Italy, Lingotto Conference Centre - Poster sessions DIA-53
AMZC - Zerr,I.; Pocchiari,M.; Collins,S.J.; Brandel,J.P.; de Pedro Cuesta,J.; Knight,R.S.G.; Bernheimer,H.; Cardone,F.; Delasnerie-Laupretre,N.; Cuadrado Corrales,N.; Ladogana,A.; Bodemer,M.; Fletcher,A.; Awan,T.; Ruiz Bremon,A.; Budka,H.; Laplanche,J.L.; Will,R.G.; Poser,S. - Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease - Neurology 2000 Sep 26; 55(6): 811-5