Structure and assembly properties of the yeast prion Ure2pBOUSSET, Luc; THUAL, Carine; BELRHALI, Hassan et al.Comptes rendus. Biologies. 2002, Vol 325, Num 1, pp 3-8, issn 1631-0691Article

Genetic prion disease : the EUROCJD experienceKOVACS, Gabor G; PUOPOLO, Maria; DELASNERIE-LAUPRETRE, Nicole et al.Human genetics. 2005, Vol 118, Num 2, pp 166-174, issn 0340-6717, 9 p.Article

Prion diseasesKNIGHT, R. S. G; WILL, R. G.Neurology in practice. 2004, Vol 75, pp i36-i42, issn 1473-7086, SUP1Article

Widespread prehistoric human cannibalism: easier to swallow?STONEKING, Mark.Trends in ecology & evolution (Amsterdam). 2003, Vol 18, Num 10, pp 489-490, issn 0169-5347, 2 p.Article

Population-level retrospective study of neurologically expressed disorders in ruminants before the onset of Bovine Spongiform Encephalopathy (BSE) in Belgium, a BSE risk III countrySAEGERMAN, C; BERKVENS, D; DELUYKER, H et al.Journal of clinical microbiology (Print). 2005, Vol 43, Num 2, pp 862-869, issn 0095-1137, 8 p.Article

Pathogenèse des maladies à prions : Maladies à prionsLACROUX, Caroline; ANDREOLETTI, Olivier.Biofutur (Puteaux). 2009, Num 302, pp 40-43, issn 0294-3506, 4 p.Article

Preimplantation exclusion of embryos at risk for prion diseasesMEINER, V; WEINBERG, N; SAFRAN, A et al.Neurology. 2006, Vol 66, Num 4, pp 607-608, issn 0028-3878, 2 p.Article

Cellular prion protein neuroprotective function: Implications in prion diseasesROUCOU, Xavier; LEBLANC, Andréa C.Journal of molecular medicine (Berlin. Print). 2005, Vol 83, Num 1, pp 3-11, issn 0946-2716, 9 p.Article

Human prion diseases : Molecular and clinical aspectsGLATZEL, Markus; STOECK, Katharina; SEEGER, Harald et al.Archives of neurology (Chicago). 2005, Vol 62, Num 4, pp 545-552, issn 0003-9942, 8 p.Article

Accelerated prion disease in the absence of interleukin-10THACKRAY, Alana M; MCKENZIE, Andrew N; KLEIN, Michael A et al.Journal of virology. 2004, Vol 78, Num 24, pp 13697-13707, issn 0022-538X, 11 p.Article

Past, present and future of bovine spongiform encephalopathy in FranceCALAVAS, D; DUCROT, C; BARON, T. G. M et al.Current Topics in Microbiology and Immunology. 2004, Vol 284, pp 51-63, issn 0070-217X, 13 p.Article

Some considerations on the kinetics of pathogenic prions formationBOTRE, Claudio; BOTRE, Francesco; MAZZEI, Franco et al.Annali dell' Istituto superiore di sanità. 2002, Vol 38, Num 2, pp 195-198, issn 0021-2571Article

Avis et recommandations sur les encéphalopathies spongiformes subaiguès transmissibles. Septembre 1999-juin 20012001, 504 p.Book

La nouvelle instruction sur les agents transmissibles non conventionnelsPELI, Gaèlle; DURBIN, Jean-Dominique; KOWALSKI, André et al.Inter bloc. 2013, Vol 32, Num 1, pp 61-63, issn 0242-3960, 3 p.Article

Interactions of prion proteins with soilLEITA, Liviana; FORNASIER, Flavio; DE NOBILI, Maria et al.Soil biology & biochemistry. 2006, Vol 38, Num 7, pp 1638-1644, issn 0038-0717, 7 p.Article

Processing of the bovine spongiform encephalopathy-specific prion protein by dendritic cellsRYBNER-BARNIER, Catherine; JACQUEMOT, Catherine; LECLERC, Claude et al.Journal of virology. 2006, Vol 80, Num 10, pp 4656-4663, issn 0022-538X, 8 p.Article

Modélisation de l'épidémie de variant de la maladie de Creutzfeldt Jakob en FranceCHADEAU, Marc.2005, non paginé [212 p.]Thesis

Dendritic cells and oral transmission of prion diseasesHUANG, Fang-Ping; MACPHERSON, G. Gordon.Advanced drug delivery reviews. 2004, Vol 56, Num 6, pp 901-913, issn 0169-409X, 13 p.Article

Prions and dentistryPORTER, Stephen R.Journal of the Royal Society of Medicine. 2002, Vol 95, Num 4, pp 178-181, issn 0141-0768Article

Nursing care of the person with sporadic Creutzfeldt-Jacob disease = Soins pour les personnes atteintes de maladie de Creutzfeldt-Jacob sporadiqueRENTZ, Clarissa.JOURNAL OF HOSPICE AND PALLIATIVE NURSING. 2008, Vol 10, Num 5, pp 272-284, issn 1522-2179, 13 p.Article

Update : Creutzfeldt-Jakob disease associated with cadaveric dura mater grafts - Japan, 1978-2008 = Mise à jour : la maladie de Creutzfeldt-Jakob associée à des greffes de dure-mère prélevée sur des cadavres - Japon, 1978-2008MMWR. Recommendations & reports (Online). 2008, Vol 57, Num 42, pp 1152-1154, issn 1545-8601, 3 p.Article

Polymorphism of PRNP codons in the normal Icelandic populationGEORGSSON, G; TRYGGVASON, T; JONASDOTTIR, A. D et al.Acta neurologica scandinavica. 2006, Vol 113, Num 6, pp 419-425, issn 0001-6314, 7 p.Article

Biochemical fingerprints of prion infection: Accumulations of aberrant full-length and N-terminally truncated PrP species are common features in mouse prion diseaseTAO PAN; POKI WONG; BINGGONG CHANG et al.Journal of virology. 2005, Vol 79, Num 2, pp 934-943, issn 0022-538X, 10 p.Article

Comparison of inflammatory and acute-phase responses in the brain and peripheral organs of the ME7 model of prion diseaseCUNNINGHAM, Colm; WILCOCKSON, David C; BOCHE, Delphine et al.Journal of virology. 2005, Vol 79, Num 8, pp 5174-5184, issn 0022-538X, 11 p.Article

Subcellular localization of disease-associated prion protein in the human brainKOVACS, Gabor G; PREUSSER, Matthias; STROHSCHNEIDER, Michaela et al.The American journal of pathology. 2005, Vol 166, Num 1, pp 287-294, issn 0002-9440, 8 p.Article