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Neurology(R) Neuroimmunology & Neuroinflammation|June 20, 2017
IgG-specific cell-based assay detects potentially pathogenic MuSK-Abs in seronegative MGSaif Huda, Patrick Waters, Mark Woodhall, et al.Frontiers in Neurology|January 29, 2021
Myelin Oligodendrocyte Glycoprotein (MOG) Antibody Positive Patients in a Multi-Ethnic Canadian CohortHelen Cross, Farahna Sabiq, Nathalie Ackermans, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 18, 2013
Autoantibody biomarkers in childhood-acquired demyelinating syndromes: results from a national surveillance cohortYael Hacohen, Michael Absoud, Mark Woodhall, et al.Brain : a Journal of Neurology|May 12, 2012
Prognostic factors and disease course in aquaporin-4 antibody-positive patients with neuromyelitis optica spectrum disorder from the United Kingdom and JapanJoanna Kitley, M Isabel Leite, Ichiro Nakashima, et al.JAMA Neurology|September 24, 2019
Serial Anti-Myelin Oligodendrocyte Glycoprotein Antibody Analyses and Outcomes in Children With Demyelinating SyndromesPatrick Waters, Giulia Fadda, Mark Woodhall, et al.Neurology(R) Neuroimmunology & Neuroinflammation|March 31, 2015
MOG cell-based assay detects non-MS patients with inflammatory neurologic diseasePatrick Waters, Mark Woodhall, Kevin C O'Connor, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|October 3, 2017
Predictors of outcome in a large retrospective cohort of patients with transverse myelitisMatteo Gastaldi, Enrico Marchioni, Paola Banfi, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|October 21, 2016
Gender effect on neuromyelitis optica spectrum disorder with aquaporin4-immunoglobulin GSung-Min Kim, Patrick Waters, Mark Woodhall, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 13, 2016
Brain lesion distribution criteria distinguish MS from AQP4-antibody NMOSD and MOG-antibody diseaseMaciej Juryńczyk, George Tackley, Yazhuo Kong, et al.Annals of the New York Academy of Sciences|January 30, 2018
Serological and experimental studies in different forms of myasthenia gravisAngela Vincent, Saif Huda, Michelangelo Cao, et al.Pageof 7