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Neuropathology : Official Journal of the Japanese Society of Neuropathology|January 12, 2005
Argyrophilic grain disease: a late-onset dementia with distinctive features among tauopathiesMarkus Tolnay, Florence ClavagueraCold Spring Harbor Perspectives in Medicine|December 13, 2016
The Prion-Like Behavior of Assembled Tau in Transgenic MiceFlorence Clavaguera, Markus Tolnay, Michel GoedertCurrent Opinion in Neurobiology|January 11, 2020
Prion-like properties of Tau assembliesFlorence Clavaguera, Charles Duyckaerts, Stéphane HaïkTrends in Neurosciences|May 25, 2010
The propagation of prion-like protein inclusions in neurodegenerative diseasesMichel Goedert, Florence Clavaguera, Markus TolnayActa Neuropathologica|September 6, 2007
Tauopathy models and human neuropathology: similarities and differencesStephan Frank, Florence Clavaguera, Markus TolnayNeuropharmacology|September 21, 2013
Intercellular transfer of tau aggregates and spreading of tau pathology: Implications for therapeutic strategiesFlorence Clavaguera, Fiona Grueninger, Markus TolnayCurrent Opinion in Neurology|February 7, 2019
The prion-like propagation hypothesis in Alzheimer's and Parkinson's diseaseCharles Duyckaerts, Florence Clavaguera, Marie-Claude PotierCurrent Neurology and Neuroscience Reports|September 15, 2014
Prion-like mechanisms in the pathogenesis of tauopathies and synucleinopathiesMichel Goedert, Ben Falcon, Florence Clavaguera, et al.Brain Pathology (Zurich, Switzerland)|April 17, 2013
"Prion-like" templated misfolding in tauopathiesFlorence Clavaguera, Isabelle Lavenir, Ben Falcon, et al.Acta Neuropathologica|September 27, 2003
Argyrophilic grain disease: molecular genetic difference to other four-repeat tauopathiesAndré R Miserez, Florence Clavaguera, Andreas U Monsch, et al.Pageof 2