Results 31 to 40 of about 168,114 (189)
MOG-expressing teratoma followed by MOG-IgG-positive optic neuritis. [PDF]
Wildemann B +5 more
europepmc +6 more sources
Background: Myelin oligodendrocyte glycoprotein immunoglobulin G (MOG-IgG) has been considered a diagnostic marker for patients with demyelinating disease, termed “MOG-IgG associated disorder” (MOGAD).
Cong Zhao +6 more
doaj +1 more source
Coexisting anti-NMDAR and MOG antibody (anti-NMDAR-IgG+/MOG-IgG+)-associated encephalitis have garnered great attention. This study aimed to perform a secondary analysis to determine the clinical features of this disease.
Jiayue Ding, Xiangyu Li, Zhiyan Tian
doaj +1 more source
A multicenter comparison of MOG-IgG cell-based assays [PDF]
To compares 3 different myelin oligodendrocyte glycoprotein-immunoglobulin G (IgG) cell-based assays (CBAs) from 3 international centers.Serum samples from 394 patients were as follows: acute disseminated encephalomyelitis (28), seronegative neuromyelitis optica (27), optic neuritis (21 single, 2 relapsing), and longitudinally extensive (10 single, 3 ...
Waters, P +11 more
openaire +2 more sources
BackgroundMyelin oligodendrocyte glycoprotein-immunoglobulin G (MOG-IgG)-associated disorders (MOGADs) have been considered as a new inflammatory disease entity of the central nervous system (CNS) and have heterogeneous clinical and imaging presentations.
Meifang Lei +10 more
doaj +1 more source
To determine whether there is a correlation between myelin oligodendrocyte glycoprotein (MOG) antibody-associated diseases and varicella zoster virus (VZV) infection.
Franziska Di Pauli +12 more
doaj +1 more source
Seroprevalence of anti‐myelin oligodendrocyte glycoprotein antibodies in adults with myelitis
Although myelitis is the second most common presentation in adults with myelin oligodendrocyte glycoprotein (MOG) antibody‐associated disease (MOGAD), studies on MOG‐IgG seroprevalence in patients with myelitis episodes are sparse.
Ki Hoon Kim +5 more
doaj +1 more source
Association of MOG-IgG Serostatus With Relapse After Acute Disseminated Encephalomyelitis and Proposed Diagnostic Criteria for MOG-IgG–Associated Disorders [PDF]
Recent studies have reported a higher relapse rate following an initial inflammatory demyelinating disorder in pediatric patients with persistent seropositivity of antibodies targeting myelin oligodendrocyte glycoprotein (MOG-IgG1). To date, the clinical implications of longitudinal MOG-IgG1 seropositivity using live cell assays with IgG1 secondary ...
A Sebastian, López-Chiriboga +17 more
openaire +2 more sources
Intrathecal Production of MOG-IgG
Myelin oligodendrocyte glycoprotein (MOG) antibody (Ab)–associated disease (MOGAD) is now a well-recognized demyelinating disease. Despite the phenotypic overlap with both multiple sclerosis and aquaporin-4 (AQP4)-Ab neuromyelitis optica spectrum disorder, cumulative clinical and immunologic evidence clearly discriminates between these conditions.
Yael Hacohen +2 more
openaire +3 more sources
MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 4: Afferent visual system damage after optic neuritis in MOG-IgG-seropositive versus AQP4-IgG-seropositive patients [PDF]
Background: Antibodies against myelin oligodendrocyte glycoprotein (MOG-IgG) have been reported in patients with aquaporin-4 antibody (AQP4-IgG)-negative neuromyelitis optica spectrum disorders (NMOSD).
Ringelstein, M. +86 more
core +2 more sources

