Results 51 to 60 of about 168,114 (189)
The establishment and application of MOG-IgG-mediated complement-dependent in vitro demyelination model [PDF]
Objective To explore the pathogenic mechanism of myelin oligodendrocyte glycoprotein-IgG(MOG-IgG)associated disorders (MOGAD) and screen the treatment drugs by establishing the MOGAD in vitro demyelination model.
Chen Yashuang, Xiao Xiuqing, Wang Shisi, Mo Yongxin, Sun Xiaobo, Zhong Xiaofen, Peng Lisheng
doaj +1 more source
ObjectiveGlial fibrillary acidic protein-immunoglobulin G (GFAP-IgG)-associated myelitis and myelin oligodendrocyte glycoprotein-IgG (MOG-IgG)-associated myelitis have rarely been compared. Therefore, this study aimed to explore the clinical, laboratory,
Mengyang Sun +5 more
doaj +1 more source
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).
Schumacher, Sophie +5 more
core +1 more source
BackgroundThe autoantibody to myelin oligodendrocyte glycoprotein (MOG), a component of the central nervous system myelin, has been identified in a subset of demyelinating diseases.
Kuniko Kohyama +5 more
doaj +1 more source
Antibodies to myelin-oligodendrocyte glycoprotein (anti-MOG-IgG) is a specific biomarker that has been detected in peripheral blood from children with acute multiple encephalomyelitis (ADEM) as well as in adults with aquaporin-4 (AQP4), associated with ...
Anastasiia K. Kalashnikova +5 more
doaj +1 more source
Supplemental material, Supplemental Table2 for Pain in AQP4-IgG-positive and MOG-IgG-positive neuromyelitis optica spectrum disorders by Susanna Asseyer, Felix Schmidt, Claudia Chien, Michael Scheel, Klemens Ruprecht, Judith Bellmann-Strobl, Alexander U ...
Judith Bellmann-Strobl (96062) +7 more
core +1 more source
MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 1: Frequency, syndrome specificity, influence of disease activity, long-term course, association with AQP4-IgG, and origin [PDF]
Background: Antibodies to myelin oligodendrocyte glycoprotein (MOG-IgG) have been suggested to play a role in a subset of patients with neuromyelitis optica and related disorders.
Hümmert, Martin W. +28 more
core +7 more sources
Supplemental material, Supplemental Table1 for Pain in AQP4-IgG-positive and MOG-IgG-positive neuromyelitis optica spectrum disorders by Susanna Asseyer, Felix Schmidt, Claudia Chien, Michael Scheel, Klemens Ruprecht, Judith Bellmann-Strobl, Alexander U ...
Judith Bellmann-Strobl (96062) +7 more
core +1 more source
Modelling MOG antibody-associated disorder and neuromyelitis optica spectrum disorder in animal models: Spinal cord manifestations. [PDF]
Antibodies to myelin oligodendrocyte glycoprotein (MOG-IgG) or aquaporin 4 (AQP4-IgG) are associated with CNS inflammatory disorders. We directly compared MOG35-55-induced experimental autoimmune encephalomyelitis exacerbated by MOG- and AQP4-IgG (versus
Bagnoud, Maud +19 more
core +1 more source
Chanomporn Narongkhananukul,1 Tanyatuth Padungkiatsagul,1 Panitha Jindahra,2 Chaiyos Khongkhatithum,3 Lunliya Thampratankul,3 Kavin Vanikieti1 1Department of Ophthalmology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand ...
Narongkhananukul C +5 more
doaj

