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Neurology|July 3, 2024
CSF Proteomics in Patients With Progressive Supranuclear PalsyAmy Wise, Jingyao Li, Mai Yamakawa, et al.Neurology|November 13, 2025
Multiple System Atrophy Without Dysautonomia: An Autopsy-Confirmed StudyIda Wilkens, Sarah Bebermeier, Johanne Heine, et al.European Journal of Neurology|July 23, 2021
Predictive modeling of spread in adult-onset isolated dystonia: Key properties and effect of tremor inclusionMeng Wang, Tolulope Sajobi, Francesca Morgante, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 19, 2019
How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsyMax-Joseph Grimm, Gesine Respondek, Maria Stamelou, et al.Alzheimer'S Research & Therapy|March 15, 2019
Lewy Body Dementia Association's Research Centers of Excellence Program: Inaugural Meeting ProceedingsBethany Peterson, Melissa Armstrong, Douglas Galasko, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 14, 2017
Which ante mortem clinical features predict progressive supranuclear palsy pathology?Gesine Respondek, Carolin Kurz, Thomas Arzberger, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2017
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteriaGünter U Höglinger, Gesine Respondek, Maria Stamelou, et al.Brain Communications|January 16, 2025
Brain aging rejuvenation factors in adults with genetic and sporadic neurodegenerative diseaseKaitlin B Casaletto, Rowan Saloner, John Kornak, et al.Research Square|April 8, 2024
Large-scale network analysis of the cerebrospinal fluid proteome identifies molecular signatures of frontotemporal lobar degenerationRowan Saloner, Adam Staffaroni, Eric Dammer, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 17, 2024
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association StudiesBjörn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt, et al.Pageof 9