Neuromyelitis optica (NMO) is an inflammatory CNS syndrome distinct from multiple
sclerosis (MS) that is associated with serum aquaporin-4 immunoglobulin G antibodies (AQP4-IgG). …

Myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a recently
identified autoimmune disorder that presents in both adults and children as CNS demyelination…

Over the past few years, new-generation cell-based assays have demonstrated a robust
association of autoantibodies to full-length human myelin oligodendrocyte glycoprotein (MOG-…

See de Seze (doi: 10.1093/brain/awx292 ) for a scientific commentary on this article. A condition
associated with an autoantibody against MOG has been recently recognized as a new …

Since its initial reports in the 19th century, neuromyelitis optica (NMO) had been thought to
involve only the optic nerves and spinal cord. However, the discovery of highly specific anti–…

Background: Neuromyelitis optica (NMO) is an uncommon, life-threatening inflammatory
demyelinating disorder. Recently, much has become known about its immunopathogenesis. …

Neuromyelitis optica and neuromyelitis optica spectrum disorders have been recently
associated with the disease-specific autoantibody aquaporin-4, thought to be pathogenic. …

Neuromyelitis optica spectrum disorder (NMOSD) is an uncommon inflammatory disease of
the central nervous system, manifesting clinically as optic neuritis, myelitis, and certain brain …

Background Neuromyelitis optica (NMO) is the first inflammatory autoimmune demyelinating
disease of the central nervous system for which a specific antigenic target has been …

Neuromyelitis optica (NMO) is an autoimmune demyelinating disease preferentially
targeting the optic nerves and spinal cord. Once regarded as a variant of multiple sclerosis (MS), …