Results 111 to 120 of about 168,114 (189)

MOG-IgG-associated disease: literature review and case report

Myelin oligodendrocyte glycoprotein (MOG-IgG)-associated disease is a rare autoimmune inflammatory demyelinating disease of the central nervous system characterized by MOG antibody-mediated damage to the myelin sheath of neurons in the brain and spinal ...
Marina V Popova, Victoria V Shishkina, Burdenko Voronezh State Medical University, Voronezh, Russia, Natalia A Ermolenko, Mariya A Yudina, Natalia V Tkachenko, Dmitry A Kolyadin, Voronezh Regional Clinical Hospital No.1, Voronezh, Russia, Valeria A Bykova   +8 more
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What proportion of AQP4-IgG-negative NMO spectrum disorder patients are MOG-IgG positive? A cross sectional study of 132 patients

, 2017
Antibodies to myelin oligodendrocyte glycoprotein (MOG-IgG) have been described in patients with neuromyelitis optica spectrum disorders (NMOSD) without aquaporin-4 antibodies (AQP4-IgG).
Hamid, Shahd HM, Daniel Whittam, Linaker, Samantha, Kerry Mutch, Samantha Linaker, Maneesh Bhojak, Mutch, Kerry, Anu Jacob, Jacob, Anu, Shahd H. M. Hamid, Kumar Das, Das, Kumar, Whittam, Daniel, Solomon, Tom, Bhojak, Maneesh, Tom Solomon   +15 more
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Real‐world clinical experience with serum MOG and AQP4 antibody testing by live versus fixed cell‐based assay

Annals of Clinical and Translational Neurology
Objective To assess the real‐world performance of a live (LCBA) versus a fixed (FCBA) cell‐based assay for the detection of serum antibodies directed against myelin oligodendrocyte glycoprotein (MOG‐IgG) and aquaporin‐4 (AQP4‐IgG).
Yana Said, Angeliki Filippatou, Conlan Tran, LuAnn Rezavi, Kai Guo, Matthew D. Smith, Yasmin Resto, John J. Chen, Peter A. Calabresi, Patrizio Caturegli, Sean J. Pittock, Eoin P. Flanagan, Elias S. Sotirchos   +12 more
doaj   +1 more source

MOG-IgG Optic Neuritis

, 2019
Optic neuritis is the most common cause of optic neuropathy in young patients, which can cause debilitating vision loss and blindness. Two novel glial autoantibodies have been discovered that better characterize a subset of patients with optic neuritis ...
John Chen, MD, PhD
core  

Clinical, Demographic, and Radiological Characteristics of Patients Demonstrating Antibodies Against Myelin Oligodendrocyte Glycoprotein

Balkan Medical Journal
Background: Optic neuritis, myelitis, and neuromyelitis optica spectrum disorder (NMOSD) have been associated with antibodies against myelin oligodendrocyte glycoprotein-immunoglobulin G (anti-MOG-IgG).
Sümeyye Koç, Sedat Şen, Yüksel Terzi, Ferah Kızılay, Serkan Demir, Dürdane Bekar Aksoy, Fatma Kurtuluş, Nuray Bilge, Egemen Idilman, Cihat Uzunköprü, Serdal Güngör, Vedat Çilingir, Özlem Ethemoğlu, Cavit Boz, Haluk Gümüş, Ahmet Kasım Kılıç, Ayşin Kısabay, Levent Sinan Bir, Ömer Faruk Turan, Aysun Soysal, Mesrure Köseoğlu, Gülnur Tekgöl Uzuner, Hasan Bayındır, Sibel Canbaz Kabay, Mustafa Çam, Vildan Yayla, Hüseyin Tan, Abdülcemal Özcan, Özlem Taşkapıoğlu, Muammer Korkmaz, Yusuf Tamam, Yılmaz İnanç, Hüsnü Efendi, Dilcan Kotan, Mehmet Fatih Yetkin, Adnan Burak Bilgiç, Hikmet Saçmacı, Serpil Demirci, Yahya Çelik, Turan Poyraz, Murat Terzi   +40 more
doaj   +1 more source

MOG-IgG Optic Neuritis (Slides)

, 2019
Optic neuritis is the most common cause of optic neuropathy in young patients, which can cause debilitating vision loss and blindness. Two novel glial autoantibodies have been discovered that better characterize a subset of patients with optic neuritis ...
John Chen, MD, PhD
core  

Characteristics of myelin oligodendrocyte glycoprotein antibody-associated meningoencephalitis

Multiple Sclerosis Journal - Experimental, Translational and Clinical
Background Meningoencephalitis can occur in myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD). Objective To assess the clinical and radiologic features of MOG-IgG meningoencephalitis.
Aisha Elfasi, Samir Alkabie, Elsa Rodriguez, Mayra Montalvo, Rhaisa Castrodad-Molina, Fernando X Cuascut, George J Hutton, Revere Kinkel, Jennifer Graves, Torge Rempe   +9 more
doaj   +1 more source

Autoantibodies against myelin oligodendrocyte glycoprotein in a subgroup of patients with psychotic symptoms

Frontiers in Neurology
The presence of autoantibodies against myelin oligodendrocyte glycoprotein (MOG) is a hallmark of MOG antibody-associated disease (MOGAD), a recently defined demyelinating disease entity presenting with core clinical features of optic neuritis, myelitis,
Nikita A. van de Burgt, Nikita A. van de Burgt, Laila Kulsvehagen, Marina Mané-Damas, Marina Mané-Damas, Luc Lutz, Anne-Catherine Lecourt, Clara Monserrat, Clara Monserrat, Anita M. Vinke, Cem İ. Küçükali, Shenghua Zong, Shenghua Zong, Carolin Hoffmann, Carolin Hoffmann, Emiliano González-Vioque, Celso Arango, Nicole K. Leibold, Nicole K. Leibold, Mario Losen, Mario Losen, Peter C. Molenaar, Peter C. Molenaar, Erdem Tüzün, Nico J. M. van Beveren, Nico J. M. van Beveren, Anna Mané, Anna Mané, Rob P. W. Rouhl, Rob P. W. Rouhl, Rob P. W. Rouhl, Therese A. M. J. van Amelsvoort, Therese A. M. J. van Amelsvoort, for Genetic Risk and Outcome of Psychosis (GROUP) Investigators, Anne-Katrin Pröbstel, Anne-Katrin Pröbstel, Anne-Katrin Pröbstel, Pilar Martinez-Martinez, Pilar Martinez-Martinez   +38 more
doaj   +1 more source

A practical alternative to live cell-based assay for AQP4 and MOG antibody detectionResearch in context

EBioMedicine
Summary: Background: Live cell-based assay (LCBA) is the gold standard for sensitive detection of aquaporin-4 (AQP4) and myelin oligodendrocyte glycoprotein (MOG) autoantibodies in neuromyelitis optica spectrum disorder (NMOSD) and MOG antibody ...
Qi Wang, Feng Chen, Yuqi Tang, Juanjuan Zhang, Zhengyu Sun, Huaxing Meng, Zhongzheng Wang, Yingtao Wang, Shaoxin Tao, Ming Lin, Yinan Zhao, Yue Huang, Junhong Guo, Yanghua Tian, Jiewen Zhang, Junwei Hao, Liang Liu   +16 more
doaj   +1 more source

Brain-targeted autoimmunity is strongly associated with Long COVID and its chronic fatigue syndrome as well as its affective symptoms

Journal of Advanced Research
Introduction: Autoimmune responses contribute to the pathophysiology of Long COVID, affective symptoms and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Objectives: To examine whether Long COVID, and its accompanying affective symptoms and
Abbas F. Almulla, Michael Maes, Bo Zhou, Hussein K. Al-Hakeim, Aristo Vojdani   +4 more
doaj   +1 more source