Comparison of MOG-IgG with AQP4-IgG lesions in mouse brain | Download Table
Diagnostic implications of MOG/AQP4 antibodies in recurrent optic neuritis
Does time equal vision in the acute treatment of a cohort of AQP4 and MOG optic neuritis? | Neurology Neuroimmunology & Neuroinflammation
Defining distinct features of anti-MOG antibody associated central nervous system demyelination | Semantic Scholar
MOG-IgG and AQP4-IgG Testing for Optic Neuritis - Insights
Binding patterns and functional properties of human antibodies to AQP4 and MOG on murine optic nerve and retina - ScienceDirect
E.U. paediatric MOG consortium consensus: Part 1 – Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders - ScienceDirect
コラム | 岐阜大学大学院医学系研究科脳神経内科学分野
Beyond Aquaporin and MOG- Novel brain reactive antibodies and B cell responses in Neuromyelitis optica spectrum disorders | Else Kröner-Fresenius-Stiftung
Neuromyelitis optica spectrum and myelin oligodendrocyte glycoprotein antibody‐related disseminated encephalomyelitis - Misu - 2019 - Clinical and Experimental Neuroimmunology - Wiley Online Library
MRI differences between MOG antibody disease and AQP4 NMOSD - Sara Salama, Majid Khan, Amirali Shanechi, Michael Levy, Izlem Izbudak, 2020
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
Spectrum of MOG antibody-associated disorders. | Download Scientific Diagram
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
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
Figure Model contrasting the potential role of antibodies to myelin oligodendrocyte glycoprotein (MOG) or aquaporin-4 (AQP4) in opticospinal inflammationMOG-specific. - ppt download
Clinical and immunological differences between MOG associated disease and anti AQP4 antibody-positive neuromyelitis optica spectrum disorders: Blood–brain barrier breakdown and peripheral plasmablasts - Multiple Sclerosis and Related Disorders
Does MOG Ig-positive AQP4-seronegative opticospinal inflammatory disease justify a diagnosis of NMO spectrum disorder? | Neurology Neuroimmunology & Neuroinflammation
Antibodies to MOG and AQP4 in children with neuromyelitis optica and limited forms of the disease | Journal of Neurology, Neurosurgery & Psychiatry
Diagnostic implications of MOG/AQP4 antibodies in recurrent optic neuritis
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
