Results 21 to 30 of about 184,937 (258)

Myelin oligodendrocyte glycoprotein antibody-associated disease presenting as isolated simultaneous bilateral optic neuritis in a child [PDF]

open access: yesOman Journal of Ophthalmology
Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is the most recently defined distinct demyelinating disorder of the central nervous system which has heterogeneous clinical manifestations.
Gurcharan Singh, Ziaur Rahman
doaj   +2 more sources

Case Report: Fundus findings in myelin oligodendrocyte glycoprotein-associated optic neuritis [PDF]

open access: yesFrontiers in Ophthalmology
Myelin oligodendrocyte glycoprotein-associated optic neuritis (MOG-ON) is a sight-threatening demyelinating disorder that can present with various ocular manifestations.
John R. Wilson   +3 more
doaj   +2 more sources

Extensive brainstem lesions in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD): A case report

open access: yesRadiology Case Reports
Myelin oligodendrocyte glycoprotein antibody-associated disease is a group of central nervous system demyelinating disorders caused by autoantibodies.
Yasuyuki Kojita, MD, PhD   +5 more
doaj   +2 more sources

Clinical and Neuroimaging Characteristics of Pediatric Acute Disseminating Encephalomyelitis With and Without Antibodies to Myelin Oligodendrocyte Glycoprotein

open access: yesFrontiers in Neurology, 2020
Objective: To compare the clinical and neuroimaging characteristics of anti-myelin oligodendrocyte glycoprotein antibody (MOG-ab) negative and positive pediatric acute disseminating encephalomyelitis (ADEM) patients.Methods: Clinical characteristics ...
Shuizhen Zhou, Lifei Yu, Linmei Zhang
exaly   +3 more sources

Myelin basic protein peptide 45–89 induces the release of nitric oxide from microglial cells. [PDF]

open access: yes, 2002
Continuous (24 h) exposure of mixed oligodendrocyte/microglial cells to peptides 45–89 derived from citrullinated C8 isoforms of myelin basic protein (MBP) induces cell death.
Pichkhadze, B.   +4 more
core   +7 more sources

The nomogram model predicts relapse risk in myelin oligodendrocyte glycoprotein antibody-associated disease: a single-center study

open access: yesFrontiers in Immunology
BackgroundMyelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is an autoimmune disorder of the central nervous system, characterized by seropositive MOG antibodies.
Meini Zhang
exaly   +3 more sources

Myelin Oligodendrocyte Glycoprotein Antibody Disease – MOGAD

open access: yesIndian Journal of Pediatrics
V. Gowda   +3 more
semanticscholar   +3 more sources

Diagnosis of myelin oligodendrocyte glycoprotein antibody-associated disease: International MOGAD Panel proposed criteria.

open access: yesLancet Neurology, 2023
Serum antibodies directed against myelin oligodendrocyte glycoprotein (MOG) are found in patients with acquired CNS demyelinating syndromes that are distinct from multiple sclerosis and aquaporin-4-seropositive neuromyelitis optica spectrum disorder ...
B. Banwell   +22 more
semanticscholar   +1 more source

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): A Review of Clinical and MRI Features, Diagnosis, and Management

open access: yesFrontiers in Neurology, 2022
Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is the most recently defined inflammatory demyelinating disease of the central nervous system (CNS).
Elia Sechi   +8 more
semanticscholar   +1 more source

Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD): current understanding and challenges

open access: yesJournal of Neurology, 2023
New diagnostic criteria for myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) have recently been proposed, distinguishing this syndrome from other inflammatory diseases of the central nervous system.
A. Al-Ani, John Chen, F. Costello
semanticscholar   +1 more source

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