1)Wynford-Thomas R, Jacob A, Tomassini V:Neurological update:MOG antibody disease. J Neurol 266:1280-1286, 2019
2)Banwell B, Bennett JL, Marignier R et al:Diagnosis of myelin oligodendrocyte glycoprotein antibody-associated disease:International MOGAD Panel proposed criteria. Lancet Neurol 22:268-282, 2023
3)Hassan MB, Stern C, Flanagan EP et al:Population-based incidence of optic neuritis in the era of aquaporin-4 and myelin oligodendrocyte glycoprotein antibodies. Am J Ophthalmol 220:110-114, 2020
4)de Mol CL, Wong Y, van Pelt ED et al:The clinical spectrum and incidence of anti-MOG-associated acquired demyelinating syndromes in children and adults. Mult Scler 26:806-814, 2020
5)Marignier R, Hacohen Y, Cobo-Calvo A et al:Myelin-oligodendrocyte glycoprotein antibody-associated disease. Lancet Neurol 20:762-772, 2021
6)Chen JJ, Flanagan EP, Jitprapaikulsan J et al:Myelin oligodendrocyte glycoprotein antibody-positive optic neuritis:clinical characteristics, radiologic clues, and outcome. Am J Ophthalmol 195:8-15, 2018
7)Sechi E, Cacciaguerra L, Chen JJ et al:Myelin oligodendrocyte glycoprotein antibody-associated disease(MOGAD):a review of clinical and MRI features, diagnosis, and management. Front Neurol 13:885218, 2022
8)Ishikawa H, Kezuka T, Shikishima K et al:Epidemiologic and clinical characteristics of optic neuritis in Japan. Ophthalmology 126:1385-1398, 2019
9)Tajfirouz DA, Bhatti MT, Chen JJ:Clinical characteristics and treatment of MOG-IgG-associated optic neuritis. Curr Neurol Neurosci Rep 19:100, 2019
10)Nakamura M, Ogawa R, Fujimori J et al:Epidemiological and clinical characteristics of myelin oligodendrocyte glycoprotein antibody-associated disease in a nationwide survey. Mult Scler 29:530-539, 2023
11)Jurynczyk M, Messina S, Woodhall MR et al:Clinical presentation and prognosis in MOG-antibody disease:a UK study. Brain 140:3128-3138, 2017