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Les maladies à prions humaines sont des maladies neurodégénératives rares et mortelles, liées à des agents pathogènes de nature protéique. La plus fréquente est la maladie de Creutzfeldt-Jakob (MCJ), qui existe sous une forme sporadique, génétique ou acquise (iatrogène ou nouvelle variante [v-MCJ]). Le diagnostic de certitude des maladies à prions humaines est fondé sur l'examen neuropathologique,...
Set the date range to filter the displayed results. You can set a starting date, ending date or both. You can enter the dates manually or choose them from the calendar.