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Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2025
AZP2006 in Progressive Supranuclear Palsy: Outcomes from a Phase 2a Multicenter, Randomized Trial, and Open-Label Extension on Safety, Biomarkers, and Disease ProgressionJean-Christophe Corvol, Mickael Alexandre Obadia, Caroline Moreau, et al.Annals of Clinical and Translational Neurology|January 12, 2025
Demyelinating neuropathy as the initial presentation of familial E200K Creutzfeldt-Jakob disease in two patientsCécile Delorme, Antoine Pégat, Julian Theuriet, et al.Human Molecular Genetics|September 12, 2012
Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disordersKatell Peoc'h, Etienne Levavasseur, Emilien Delmont, et al.Neurology|February 27, 2020
Autoantibodies against the prion protein in individuals with PRNP mutationsKarl Frontzek, Manfredi Carta, Marco Losa, et al.JAMA Network Open|January 31, 2022
Validation of Revised International Creutzfeldt-Jakob Disease Surveillance Network Diagnostic Criteria for Sporadic Creutzfeldt-Jakob DiseaseNeil Watson, Peter Hermann, Anna Ladogana, et al.Neurobiology of Aging|December 6, 2011
Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob riskPascual Sanchez-Juan, Matthew T Bishop, Yurii S Aulchenko, et al.BMC Public Health|November 14, 2006
Human transmissible spongiform encephalopathies in eleven countries: diagnostic pattern across time, 1993-2002Jesús de Pedro-Cuesta, Markus Glatzel, Javier Almazán, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 14, 2019
Examining the Reserve Hypothesis in Parkinson's Disease: A Longitudinal StudyPei-Chen Lee, Fanny Artaud, Florence Cormier-Dequaire, et al.Neurology|June 22, 2018
Longitudinal analysis of impulse control disorders in Parkinson diseaseJean-Christophe Corvol, Fanny Artaud, Florence Cormier-Dequaire, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 23, 2013
Intensity of human prion disease surveillance predicts observed disease incidenceGenevieve M J A Klug, Handan Wand, Marion Simpson, et al.Pageof 7