Inflammatory myelopathies can manifest with a combination of motor, sensory and
autonomic dysfunction of variable severity. Depending on the underlying etiology, the …

Importance Recent studies have reported a higher relapse rate following an initial
inflammatory demyelinating disorder in pediatric patients with persistent seropositivity of …

Mycophenolate mofetil (MMF) is an immunosuppressive agent (IS) which is widely
prescribed in neuromyelitis optica spectrum disorder (NMOSD) patients. We aim to assess …

Purpose To characterize the clinical phenotype of myelin oligodendrocyte glycoprotein
antibody (MOG-IgG) optic neuritis. Design Observational case series. Methods Setting …

Importance Recognizing the characteristics of myelin oligodendrocyte glycoprotein
autoantibody (MOG-IgG) myelitis is essential for early accurate diagnosis and treatment …

Objective Myelin oligodendrocyte glycoprotein–immunoglobulin G (MOG-IgG) associated
disorder (MOGAD) often manifests with recurrent CNS demyelinating attacks. The optimal …

Importance Autoantibodies to aquaporin-4 (AQP4) and myelin oligodendrocyte glycoprotein
(MOG) are recently established biomarkers of autoimmune optic neuritis whose frequency …

Importance Recognizing the presenting and immunopathological features of Kelch-like
protein-11 immunoglobulin G seropositive (KLHL11 IgG+) patients may aid in early …

Purpose To determine the aquaporin-4 and myelin oligodendrocyte glycoprotein (MOG)
immunoglobulin G (IgG) serostatus and visual outcomes in patients with recurrent optic …

Objective To conduct systematic review and meta‐analysis for the efficacy of therapeutic
plasma exchange (TPE) for neuromyelitis optica spectrum disorder (NMOSD) with an acute …