MOG Antibody Disease: Nuances in Presentation, Diagnosis, and Management

KA Stefan, JR Ciotti - Current Neurology and Neuroscience Reports, 2024 - Springer
MOGAD pathophysiology informs some of the relatively unique clinical and radiologic
features which have come to define this condition, and similarly has implications for …

Clinical characterization and ancillary tests in Susac syndrome: a systematic review

A Wilf-Yarkoni, O Zmira, A Tolkovsky… - Neurology …, 2024 - AAN Enterprises
Susac syndrome (SuS) is an orphan microangiopathic disease characterized by a triad of
encephalopathy, visual disturbances due to branch retinal artery occlusions, and …

Radiologic Lag and Brain MRI Lesion Dynamics During Attacks in MOG Antibody–Associated Disease

L Cacciaguerra, O Abdel-Mannan, D Champsas… - Neurology, 2024 - AAN Enterprises
Background and Objectives Knowledge of the evolution of CNS demyelinating lesions within
attacks could assist diagnosis. We evaluated intra-attack lesion dynamics in patients with …

Characteristics of aseptic meningitis-like attack—an underestimated phenotype of myelin oligodendrocyte glycoprotein antibody-associated disease

M Gu, X Mo, Z Fang, H Zhang, W Lu, X Shen… - Multiple Sclerosis and …, 2023 - Elsevier
Introduction Aseptic meningitis was recently reported and recognized as a novel phenotype
of Myelin oligodendrocyte glycoprotein antibody-associated disease (MOG-AD). However …

Grey Matter Atrophy and its Relationship with White Matter Lesions in Patients with Myelin Oligodendrocyte Glycoprotein Antibody‐associated Disease, Aquaporin‐4 …

R Cortese, M Battaglini, F Prados, G Gentile… - Annals of …, 2024 - Wiley Online Library
Objective To evaluate:(1) the distribution of gray matter (GM) atrophy in myelin
oligodendrocyte glycoprotein antibody‐associated disease (MOGAD), aquaporin‐4 antibody …

Leptomeningeal Enhancement in Pediatric Anti-Myelin Oligodendrocyte Glycoprotein Antibody Disease, Multiple Sclerosis, and Neuromyelitis Optica Spectrum …

A Goldman-Yassen, A Lee, G Gombolay - Pediatric Neurology, 2024 - Elsevier
Background Anti-myelin oligodendrocyte glycoprotein (MOG) antibody disease (MOGAD) is
a type of acquired demyelinating disease that is distinct from multiple sclerosis (MS) and …

Diagnostic Criteria for Multiple Sclerosis, Neuromyelitis Optica Spectrum Disorders, and Myelin Oligodendrocyte Glycoprotein–immunoglobulin G-associated Disease

M Filippi, P Preziosa, M Margoni… - Neuroimaging …, 2024 - neuroimaging.theclinics.com
MR imaging plays a crucial role in the diagnostic evaluation of patients suspected of having
multiple sclerosis (MS) or other inflammatory demyelinating disorders affecting the central …

Updates in NMOSD and MOGAD diagnosis and treatment: a tale of two central nervous system autoimmune inflammatory disorders

L Cacciaguerra, EP Flanagan - Neurologic clinics, 2024 - neurologic.theclinics.com
Aquaporin-4-IgG positive neuromyelitis optica spectrum disorder (AQP4+ NMOSD) and
myelin-oligodendrocytes glycoprotein antibody-associated disease (MOGAD) a Department …

[PDF][PDF] Rosa Cortese, MD, PhD, Marco Battaglini, PhD, Ferran Prados, PhD, 2, 4, 5 Giordano Gentile, PhD, Ludovico Luchetti, BASc, Alessia Bianchi, MD, PhD, 2 Lukas …

F Durand-Dubief, C de Medeiros Rimkus, SLA Pereira… - 2024 - researchgate.net
Objective: To evaluate:(1) the distribution of gray matter (GM) atrophy in myelin
oligodendrocyte glycoprotein antibody-associated disease (MOGAD), aquaporin-4 antibody …

Anti-NMDAR encephalitis with MOGAD overlap syndrome, isolated epilepsy, and unilateral thalamus changes: a case report and literature review

R Zhong, X Chen, F Liao, Z Lin, Z Zhang, Y Chen, L Cui - 2023 - researchsquare.com
Background Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is an
autoimmune brain disease mediated by antibodies and characterized by psychiatric …