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

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 …

Objective To describe clinical and radiologic features associated with myelin
oligodendrocyte glycoprotein antibodies (MOG-Ab) in a large French nationwide adult …

Neuromyelitis optica (NMO, Devic's syndrome), long considered a clinical variant of multiple
sclerosis, is now regarded as a distinct disease entity. Major progress has been made in the …

Neuromyelitis optica is an inflammatory demyelinating disorder of the CNS. The discovery of
circulating IgG1 antibodies against the astrocyte water channel protein aquaporin 4 (AQP4) …

MS is heterogeneous with respect to clinical, genetic, radiographic, and pathologic features;
surrogate MRI, clinical, genetic, serologic, and/or CSF markers for each of the four …

Neuromyelitis optica (NMO) is a disabling autoimmune astrocytopathy characterized by
typically severe and recurrent attacks of optic neuritis and longitudinally extensive myelitis …

There has been significant progress in our understanding of the pathology and
pathogenesis of central nervous system inflammatory demyelinating diseases …

Objective To define the frequency, duration, and severity of intractable nausea, vomiting, or
hiccups in aquaporin-4–immunoglobulin G (AQP4-IgG)-positive neuromyelitis optica …

The discovery of a novel serum autoantibody (termed NMO-IgG or AQP4-Ab) in a subset of
patients in 2004 has revived interest in neuromyelitis optica (NMO). While the history of …