Neuromyelitis optica spectrum disorder and myelin oligodendrocyte glycoprotein associated disorder-optic neuritis: a comprehensive review of diagnosis and …

SM Gospe III, JJ Chen, MT Bhatti - Eye, 2021 - nature.com
Optic neuritis (ON) is the most common cause of acute optic neuropathy in patients younger
than 50 years of age and is most frequently idiopathic or associated with multiple sclerosis …

The influence of MOGAD on diagnosis of multiple sclerosis using MRI

R Geraldes, G Arrambide, B Banwell, À Rovira… - Nature Reviews …, 2024 - nature.com
Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is an
immune-mediated demyelinating disease that is challenging to differentiate from multiple …

Neutrophil-mediated mechanisms of damage and in-vitro protective effect of colchicine in non-vascular Behçet's syndrome

A Bettiol, M Becatti, E Silvestri… - Clinical & …, 2021 - academic.oup.com
Behçet's syndrome (BS) is a systemic vasculitis with several clinical manifestations.
Neutrophil hyperactivation mediates vascular BS pathogenesis, via both a massive reactive …

Monkeypox‐Associated Central Nervous System Disease: A Case Series and Review

KM Money, TA Barnett, S Rapaka, R Osborn… - Annals of …, 2023 - Wiley Online Library
Objective Monkeypox virus (MPXV) disease has been declared a public health emergency
by the World Health Organization, creating an urgent need for neurologists to be able to …

Assessment of international MOGAD diagnostic criteria in patients with overlap** MOG-associated disease and multiple sclerosis phenotypes

GS Manzano, M Levy, R Salky, FJ Mateen… - Journal of …, 2024 - Springer
Background The clinical spectrum and diagnosis of myelin oligodendrocyte glycoprotein
antibody-associated disease (MOGAD) has evolved in the setting of an optimized anti-MOG …

Susceptibility-based imaging aids accurate distinction of pediatric-onset MS from myelin oligodendrocyte glycoprotein antibody-associated disease

S Sacco, A Virupakshaiah, N Papinutto… - Multiple Sclerosis …, 2023 - journals.sagepub.com
Background: Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease
(MOGAD) and pediatric-onset multiple sclerosis (POMS) share clinical and magnetic …

Evidence for and against subclinical disease activity and progressive disease in MOG antibody disease and neuromyelitis optica spectrum disorder

N Molazadeh, AG Filippatou, ES Vasileiou… - Journal of …, 2021 - Elsevier
Myelin oligodendrocyte glycoprotein antibody disease (MOGAD) and aquaporin-4 IgG
seropositive neuromyelitis optica spectrum disorder (AQP4-IgG+ NMOSD) are generally …

MRI to differentiate multiple sclerosis, neuromyelitis optica, and myelin oligodendrocyte glycoprotein antibody disease

E Carnero Contentti, DT Okuda, JI Rojas… - Journal of …, 2023 - Wiley Online Library
Differentiating multiple sclerosis (MS) from other relapsing inflammatory autoimmune
diseases of the central nervous system such as neuromyelitis optica spectrum disorder …

Magnetic resonance imaging in neuromyelitis optica spectrum disorder

L Clarke, S Arnett, K Lilley, J Liao… - Clinical & …, 2021 - academic.oup.com
Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory disease of the central
nervous system (CNS) associated with antibodies to aquaporin-4 (AQP4), which has distinct …

Plasma complement 3 and complement 4 are promising biomarkers for distinguishing NMOSD from MOGAD and are associated with the blood-brain-barrier …

L Lin, Y Wu, H Hang, J Lu, Y Ding - Frontiers in Immunology, 2022 - frontiersin.org
Background and Objective Neuromyelitis optica spectrum disorders (NMOSD) and myelin
oligodendrocyte glycoprotein antibody (MOG-IgG) associated disease (MOGAD) are …