Background Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is
a newly described clinical entity comprised of isolated or recurrent attacks of optic neuritis …

Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to
steroids (CLIPPERS) is a distinct pathologic entity of unknown etiology. Here, we describe …

Background: A considerable number of patients with myelin oligodendrocyte glycoprotein
antibody–associated disease (MOGAD) will experience a relapse, but the effect of …

We present a patient with positive medium titer MOG-IgG and progressive neurological
decline whose clinical and radiological phenotype were not consistent with a MOG-IgG …

Purpose of review Myelin oligodendrocyte glycoprotein antibody-associated disease
(MOGAD) is a rare inflammatory disorder of the central nervous system that affects both …

Background MOG-IgG-associated disease (MOGAD) in adults typically presents as a
monophasic or relapsing optic, spinal, or opticospinal neuroinflammatory syndrome. Current …

Myelin oligodendrocyte glycoprotein-immunoglobulin G associated disease (MOGAD) is an
autoimmune demyelinating disorder of the central nervous system (CNS) which usually …

Background While many patients with myelin oligodendrocyte glycoprotein antibody-
mediated disease (MOG-AD) will have a monophasic course, 30-80% of patients will …

Monoclonal antibody therapies mark the new era of targeted treatment for relapse
prevention in aquaporin-4 (AQP4)-immunoglobulin G (IgG)-positive neuromyelitis optica …

CRION is an inflammatory optic neuropathy that is characterized by a chronic and relapsing
course, that is characterized by pain associated with subacute vision loss. It is favorably …