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

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 Structural retinal imaging biomarkers are important for early recognition and
monitoring of inflammation and neurodegeneration in multiple sclerosis. With the introduction …

Background The diagnostic and pathophysiological relevance of antibodies to aquaporin-4 (AQP4-Ab)
in patients with neuromyelitis optica spectrum disorders (NMOSD) has been …

Background A subset of patients with neuromyelitis optica spectrum disorders (NMOSD)
has been shown to be seropositive for myelin oligodendrocyte glycoprotein antibodies (MOG-…

… Changes in the intracellular redox state have been observed during the self-renewal and
differentiation processes of dividing O-2A progenitor cells 6 ; however, the molecular …

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-…

Interferon (IFN)-induced immunoproteasomes (i-proteasomes) have been associated with
improved processing of major histocompatibility complex (MHC) class I antigens. Here, we …

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 …

A new metallization scheme has been developed for obtaining very low Ohmic contact to n‐GaN.
The metallization technique involves the deposition of a composite metal layer Ti/Al/Ni/…