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Handbook of Clinical Neurology|June 12, 2018
Variant Creutzfeldt-Jakob diseaseJean-Philippe Brandel, Richard KnightJournal of Neurochemistry|July 28, 2011
Biochemical and strain properties of CJD prions: complexity versus simplicityStéphane Haïk, Jean-Philippe BrandelInfection, 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 BrandelBulletin De L'Academie Nationale De Medecine|June 15, 2018
History of Prions and transmission of protein misfoldingJean-Jacques Hauw, Stéphane Haik, Jean-Philippe BrandelBrain Communications|November 13, 2023
Validation of the Medical Research Council prion disease rating scale in FranceJean-Philippe Brandel, Arlette Welaratne, Angeline Denouel, et al.Movement Disorders Clinical Practice|August 29, 2025
Clinical Impact of Switching from Subcutaneous Apomorphine to Foslevodopa/Foscarbidopa in Advanced Parkinson's Disease: A Real-World Observational Study (FOSAPO)Clément Desjardins, Quentin Salardaine, Jean-Philippe Brandel, et al.Neurology|July 21, 2006
Iatrogenic Creutzfeldt-Jakob disease: the waning of an eraPaul Brown, Jean-Philippe Brandel, Michael Preece, 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.Psychologie & Neuropsychiatrie Du Vieillissement|September 13, 2008
[Creutzfeldt-Jakob disease in patients before and after 80 years of age]Jean-Philippe Brandel, Dominique Salomon, Jean-Jacques Hauw, et al.Pageof 20