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European Journal of Neurology|February 9, 2026
MOGAD in South Wales: Diagnostic Evolution and Disease EpidemiologySophie Voase, Patrick Waters, Stephen Jolles, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 19, 2013
Utility of aquaporin-4 antibody assay in patients with neuromyelitis optica spectrum disordersSung-Min Kim, Patrick Waters, Mark Woodhall, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|February 8, 2023
Antibodies Produced by CLL Phenotype B Cells in Patients With Myasthenia Gravis Are Not Directed Against Neuromuscular EndplatesFlorian Ingelfinger, Michael Kramer, Mirjam Lutz, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 26, 2016
Chronic neuropathic pain severity is determined by lesion level in aquaporin 4-antibody-positive myelitisGeorge Tackley, Domizia Vecchio, Shahd Hamid, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 6, 2014
Paediatric neuromyelitis optica: clinical, MRI of the brain and prognostic featuresMichael Absoud, Ming J Lim, Richard Appleton, et al.
Neurology|February 8, 2019
A multicenter comparison of MOG-IgG cell-based assaysPatrick J Waters, Lars Komorowski, Mark Woodhall, et al.
Frontiers in Neurology|October 23, 2019
AQP4 Antibody Assay Sensitivity Comparison in the Era of the 2015 Diagnostic Criteria for NMOSDKerri Prain, Mark Woodhall, Angela Vincent, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 18, 2022
Serum MOG-IgG in children meeting multiple sclerosis diagnostic criteriaGiulia Fadda, Patrick Waters, Mark Woodhall, et al.
European Neurology|February 23, 2013
Progressive encephalomyelitis with rigidity and myoclonus: a syndrome with diverse clinical features and antibody responsesErkingül Shugaiv, Maria Isabel Leite, Elçin Şehitoğlu, et al.
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