The spectrum of MOG autoantibody-associated demyelinating diseases | Nature Reviews Neurology
MOG antibody prevalence in adult optic neuritis and clinical predictive factors for diagnosis: a Chinese cohort study - Multiple Sclerosis and Related Disorders
MOG-IgG and AQP4-IgG Testing for Optic Neuritis - Insights
MRI differences between MOG antibody disease and AQP4 NMOSD - Sara Salama, Majid Khan, Amirali Shanechi, Michael Levy, Izlem Izbudak, 2020
Figure Model contrasting the potential role of antibodies to myelin oligodendrocyte glycoprotein (MOG) or aquaporin-4 (AQP4) in opticospinal inflammationMOG-specific. - ppt download
Diagnostic implications of MOG/AQP4 antibodies in recurrent optic neuritis
Vicente Martín on Twitter: "MOG in NMOSD Patients They have a different immunopathogenic mechanism in MOG-IgG–positive Neuromyelitis Optica Spectrum Disorders patients With some clinical, epidemiologic, and radiologic features distinct from those in
Comparison of MOG-IgG with AQP4-IgG lesions in mouse brain | Download Table
IJMS | Free Full-Text | Cells to the Rescue: Emerging Cell-Based Treatment Approaches for NMOSD and MOGAD | HTML
Frontiers | MOG-IgG-Associated Optic Neuritis, Encephalitis, and Myelitis: Lessons Learned From Neuromyelitis Optica Spectrum Disorder
Different magnetic resonance imaging features between MOG antibody- and AQP4 antibody-mediated disease: A Chinese cohort study - Journal of the Neurological Sciences
Quantitative brain lesion distribution may distinguish MOG-ab and AQP4-ab neuromyelitis optica spectrum disorders | SpringerLink
Pathology of myelin oligodendrocyte glycoprotein antibody–associated disease - Misu - 2021 - Clinical and Experimental Neuroimmunology - Wiley Online Library
Beyond Aquaporin and MOG- Novel brain reactive antibodies and B cell responses in Neuromyelitis optica spectrum disorders | Else Kröner-Fresenius-Stiftung
Does MOG Ig-positive AQP4-seronegative opticospinal inflammatory disease justify a diagnosis of NMO spectrum disorder? | Neurology Neuroimmunology & Neuroinflammation
Clinicoradiological comparative study of Aquaporin-4-IgG seropositive neuromyelitis optica spectrum disorder (NMOSD) and MOG antibody associated disease (MOGAD): A prospective observational study and review of literature - ScienceDirect
E.U. paediatric MOG consortium consensus: Part 1 – Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders - ScienceDirect
Complement activating antibodies to myelin oligodendrocyte glycoprotein in neuromyelitis optica and related disorders | Journal of Neuroinflammation | Full Text
Binding patterns and functional properties of human antibodies to AQP4 and MOG on murine optic nerve and retina - ScienceDirect
Brain lesions caused by MOG-IgG and AQP4-IgG. Mice received... | Download Scientific Diagram
Diagnostic implications of MOG/AQP4 antibodies in recurrent optic neuritis
Neurological update: MOG antibody disease | SpringerLink
MRI features of MOG-IgG and AQP4-IgG seropositive patients with NMOSD | Download Table
Anti-MOG antibodies are present in a subgroup of patients with a neuromyelitis optica phenotype. - Abstract - Europe PMC
Spectrum of MOG antibody-associated disorders. | Download Scientific Diagram
Frontiers | Comparative Analysis of T-Cell Responses to Aquaporin-4 and Myelin Oligodendrocyte Glycoprotein in Inflammatory Demyelinating Central Nervous System Diseases
Does MOG Ig-positive AQP4-seronegative opticospinal inflammatory disease justify a diagnosis of NMO spectrum disorder? | Neurology Neuroimmunology & Neuroinflammation
