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Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|June 24, 2014
Infectious prion diseases in humans: cannibalism, iatrogenicity and zoonosesStéphane Haïk, Jean-Philippe BrandelJournal of Neurochemistry|July 28, 2011
Biochemical and strain properties of CJD prions: complexity versus simplicityStéphane Haïk, Jean-Philippe BrandelViruses|March 13, 2019
In vitro Modeling of Prion Strain TropismEtienne Levavasseur, Nicolas Privat, Stéphane HaïkCurrent Opinion in Neurobiology|January 11, 2020
Prion-like properties of Tau assembliesFlorence Clavaguera, Charles Duyckaerts, Stéphane HaïkBrain Communications|November 13, 2023
Validation of the Medical Research Council prion disease rating scale in FranceJean-Philippe Brandel, Arlette Welaratne, Angeline Denouel, et al.Neurology|July 27, 2018
Susceptibility to Creutzfeldt-Jakob disease after human growth hormone treatment in FranceLaurène Peckeu, Jean-Philippe Brandel, Arlette Welaratne, et al.Journal of Virology|December 21, 2012
Prion propagation and toxicity occur in vitro with two-phase kinetics specific to strain and neuronal typeSamia Hannaoui, Layal Maatouk, Nicolas Privat, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|July 28, 2019
Factors Influencing the Incubation of an Infectious Form of Creutzfeldt-Jakob DiseaseLaurène Peckeu, Jean-Philippe Brandel, Arlette Welaratne, et al.Biological Chemistry|April 5, 2003
Different isoforms of the non-integrin laminin receptor are present in mouse brain and bind PrPSteve Simoneau, Stéphane Haïk, Christoph Leucht, et al.Joint Bone Spine|January 26, 2010
Creutzfeldt-Jakob disease in a patient treated by etanercept for rheumatoid arthritis (RA): just a coincidence?Martin Soubrier, Stéphane Haïk, Jean-Jacques Hauw, et al.Pageof 7