| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Tosi Sai, Keisuke Imai, Takehiro Yamada, Masanori Cho, Atsushi Yamamoto, Testuya Iok. [A case of paroxysmal dysarthria and ataxia appeared late after treatment of myelin oligodendrocyte glycoprotein (MOG) antibody-related isolated rhombencephalitis]. Rinsho shinkeigaku = Clinical neurology. 2024-12-18. PMID:39694520. |
[a case of paroxysmal dysarthria and ataxia appeared late after treatment of myelin oligodendrocyte glycoprotein (mog) antibody-related isolated rhombencephalitis]. |
2024-12-18 |
2024-12-21 |
Not clear |
| Tosi Sai, Keisuke Imai, Takehiro Yamada, Masanori Cho, Atsushi Yamamoto, Testuya Iok. [A case of paroxysmal dysarthria and ataxia appeared late after treatment of myelin oligodendrocyte glycoprotein (MOG) antibody-related isolated rhombencephalitis]. Rinsho shinkeigaku = Clinical neurology. 2024-12-18. PMID:39694520. |
based on the positive for anti myelin oligodendrocyte glycoprotein (mog) antibody in the serum, she was ultimately diagnosed with mog related rhombencephalitis and discharged to her home on the 45th day. |
2024-12-18 |
2024-12-21 |
Not clear |
| Reza Taghipour-Mirakmahaleh, Françoise Morin, Yu Zhang, Louis Bourhoven, Louis-Charles Béland, Qun Zhou, Julie Jaworski, Anna Park, Juan Manuel Dominguez, Jacques Corbeil, Eoin P Flanagan, Romain Marignier, Catherine Larochelle, Steven Kerfoot, Luc Vallière. Turncoat antibodies unmasked in a model of autoimmune demyelination: from biology to therapy. bioRxiv : the preprint server for biology. 2024-12-16. PMID:39677612. |
here we report the discovery of autoantibody-secreting extrafollicular plasmablasts in eae induced with specific myelin oligodendrocyte glycoprotein (mog) antigens. |
2024-12-16 |
2024-12-21 |
mouse |
| Ryotaro Ikeguchi, Natsuki Kanda, Masaki Kobayashi, Kenta Masui, Masayuki Nitta, Tatsuro Misu, Yoshihiro Muragaki, Takakazu Kawamata, Noriyuki Shibata, Kazuo Kitagawa, Yuko Shimiz. CNS B cell infiltration in tumefactive anti-myelin oligodendrocyte glycoprotein antibody-associated disease. Multiple sclerosis journal - experimental, translational and clinical. vol 10. issue 4. 2024-12-09. PMID:39651331. |
few studies have examined b cells among patients with anti-myelin oligodendrocyte glycoprotein (mog) antibody-associated disease (mogad), including brain pathology. |
2024-12-09 |
2024-12-12 |
Not clear |
| Raheem Remtulla, Sanjoy Kumar Das, Leonard A Levi. In Silico Modeling of Myelin Oligodendrocyte Glycoprotein Disulfide Bond Reduction by Phosphine-Borane Complexes. Pharmaceuticals (Basel, Switzerland). vol 17. issue 11. 2024-11-27. PMID:39598329. |
proteomic evidence suggests that myelin oligodendrocyte glycoprotein (mog) is a potential target. |
2024-11-27 |
2024-11-29 |
Not clear |
| Samuel Pace, Silvia Messina, Bo Chen, Radu Tanasescu, Athanasios Papathanasiou, Cris S Constantinescu, Maria I Leite, Mark D Willis, Janet A Johnston, Jacqueline Palace, Ruth Dobso. Cerebral cortical encephalitis in adults with myelin oligodendrocyte glycoprotein antibody-associated disease: A national case series. European journal of neurology. 2024-11-19. PMID:39560205. |
myelin oligodendrocyte glycoprotein (mog) antibody-associated disease (mogad) is a relatively recently described disease, most commonly presenting with optic neuritis and longitudinally extensive transverse myelitis. |
2024-11-19 |
2024-11-22 |
Not clear |
| Mary Anne Poovathinga. The Varying Faces of MOGAD: A Case Series. Annals of African medicine. 2024-11-08. PMID:39513417. |
myelin oligodendrocyte glycoprotein-immunoglobulin g (mog-igg)-associated disease (mogad) is an immune mediated demyelinating disorder initially described as a subtype of neuromyelitis optica spectrum disorder with antibodies against mog. |
2024-11-08 |
2024-11-16 |
Not clear |
| Aparna Srinivasan, Isaac Baldwin, Joshua R Smit. A Case of Catatonia in a 37-Month-Old Child With MOG-Antibody-Positive Acute Disseminated Encephalomyelitis. Journal of the American Academy of Child and Adolescent Psychiatry. 2024-10-31. PMID:39413967. |
in this letter to the editor, we examine a case of catatonia in a 37-month-old child with myelin oligodendrocyte glycoprotein (mog) antibody-positive acute disseminated encephalomyelitis (adem). |
2024-10-31 |
2024-11-02 |
Not clear |
| Ahmed Elashmawy, Anas Haq, Saima Sharif, Kevin Daz. A Case of Myelin Oligodendrocyte Glycoprotein Antibody Disease in a Pediatric Patient: Clinical Presentation, Treatment Response, and Follow-Up Considerations. Cureus. vol 16. issue 9. 2024-10-31. PMID:39479073. |
myelin oligodendrocyte glycoprotein antibody disease (mogad) is a rare autoimmune demyelinating disorder that targets the central nervous system and is characterized by antibodies that act against myelin oligodendrocyte glycoprotein (mog). |
2024-10-31 |
2024-11-02 |
Not clear |
| Michail Papantoniou, Georgia Panagou, Konstantinos Kanavoura. Clinical, Lab, and Radiological Evolution of an Adult Patient With Unilateral Cortical Lesion in Anti-Myelin Oligodendrocyte Glycoprotein (MOG)-Associated Encephalitis With Seizures and Anti-Glial Fibrillary Acidic Protein (GFAP) Positive Antibodies. Cureus. vol 16. issue 9. 2024-10-31. PMID:39479094. |
clinical, lab, and radiological evolution of an adult patient with unilateral cortical lesion in anti-myelin oligodendrocyte glycoprotein (mog)-associated encephalitis with seizures and anti-glial fibrillary acidic protein (gfap) positive antibodies. |
2024-10-31 |
2024-11-02 |
Not clear |
| Michail Papantoniou, Georgia Panagou, Konstantinos Kanavoura. Clinical, Lab, and Radiological Evolution of an Adult Patient With Unilateral Cortical Lesion in Anti-Myelin Oligodendrocyte Glycoprotein (MOG)-Associated Encephalitis With Seizures and Anti-Glial Fibrillary Acidic Protein (GFAP) Positive Antibodies. Cureus. vol 16. issue 9. 2024-10-31. PMID:39479094. |
myelin oligodendrocyte glycoprotein (mog) antibody-associated disease refers to a clinical and radiological spectrum of demyelinating disorders of the central nervous system. |
2024-10-31 |
2024-11-02 |
Not clear |
| Tomoya Shibahara, Kei Yamanaka, Mikiaki Matsuoka, Masaki Tachibana, Junya Kuroda, Hiroshi Nakan. Evaluation of arterial spin labeling in the diagnosis and monitoring of myelin oligodendrocyte glycoprotein-associated cerebral cortical encephalitis. Multiple sclerosis (Houndmills, Basingstoke, England). 2024-10-30. PMID:39473173. |
myelin oligodendrocyte glycoprotein (mog)-associated disorders are inflammatory demyelinating diseases of the cns. |
2024-10-30 |
2024-11-02 |
Not clear |
| Worapot Srimanan, Yaninsiri Ngathaweesu. A Rare Presentation of Myelin Oligodendrocyte Glycoprotein-Associated Optic Neuritis with Venous Stasis Retinopathy and Premacular Hemorrhage: A Case Report. Case reports in ophthalmology. vol 15. issue 1. 2024-10-30. PMID:39474012. |
myelin oligodendrocyte glycoprotein (mog)-associated disorders can cause inflammation of the central nervous system in various specific organs. |
2024-10-30 |
2024-11-02 |
Not clear |
| Sakir Necat Yilmaz, Katharina Steiner, Josef Marksteiner, Klaus Faserl, Mathias Villunger, Bettina Sarg, Christian Humpe. From Organotypic Mouse Brain Slices to Human Alzheimer's Plasma Biomarkers: A Focus on Nerve Fiber Outgrowth. Biomolecules. vol 14. issue 10. 2024-10-26. PMID:39456259. |
after a 2-week culture period, we performed immunolabeling for neurofilament and myelin oligodendrocyte glycoprotein (mog) to visualize newly formed nerve fibers and oligodendrocytes. |
2024-10-26 |
2024-10-29 |
mouse |
| Seongmi Kim, Suin Lee, Yeon Hak Chung, Hyunjin Ju, Yeon-Lim Suh, Ju-Hong Mi. Myelin oligodendrocyte glycoprotein antibody-associated disease with histopathologic features of primary CNS angiitis without demyelination: Case report and literature review. Journal of neuroimmunology. vol 396. 2024-10-24. PMID:39447418. |
primary angiitis of the central nervous system (pacns) is a rare inflammatory disease that affects both small- and medium-sized vessels of the cns, while myelin oligodendrocyte glycoprotein (mog) antibody-associated disease (mogad) is a novel antibody-mediated inflammatory demyelinating disorder that causes damage to the myelin in cns. |
2024-10-24 |
2024-10-28 |
Not clear |
| Jonathan D Krett, Angeliki G Filippatou, Paula Barreras, Carlos A Pardo, Allan C Gelber, Elias S Sotircho. "Lupus Myelitis" Revisited: A Retrospective Single-Center Study of Myelitis Associated With Rheumatologic Disease. Neurology(R) neuroimmunology & neuroinflammation. vol 12. issue 1. 2024-10-23. PMID:39442039. |
previous reports of patients with myelitis associated with rheumatologic disease may have had unrecognized aquaporin-4 (aqp4)-igg seropositive neuromyelitis optica spectrum disorder (nmosd) or myelin oligodendrocyte glycoprotein (mog)-igg-associated disease (mogad). |
2024-10-23 |
2024-10-26 |
Not clear |
| Ana Lídia Neves, Andrea Cabral, Catarina Serrão, Daniela Santos Oliveira, Janice Alves, José Miguel Alves, Mafalda Soares, Ernestina Santos, Mafalda Seabra, Helena Felgueiras, João Ferreira, Eva Brandão, Rui Guerreiro, Carla Cecília Nunes, Filipa Ladeira, José Vale, Maria José Sá, André Jorg. Blood neutrophils, oligoclonal bands and bridging corticosteroids as predictive factors for MOGAD course: Insights from a multicentric Portuguese cohort. Multiple sclerosis and related disorders. vol 92. 2024-10-20. PMID:39427600. |
myelin oligodendrocyte glycoprotein (mog) antibody-associated disease (mogad) is a heterogeneous entity with either a monophasic or relapsing course. |
2024-10-20 |
2024-10-23 |
Not clear |
| Jihane Frikeche, Marion David, Xavier Mouska, Damien Treguer, Yue Cui, Sandrine Rouquier, Enora Lecorgne, Emma Proics, Papa Babacar Fall, Audrey Lafon, Gregory Lara, Alexandra Menardi, David Fenard, Tobias Abel, Julie Gertner-Dardenne, Maurus de la Rosa, Celine Dumon. MOG-specific CAR Tregs: a novel approach to treat multiple sclerosis. Journal of neuroinflammation. vol 21. issue 1. 2024-10-20. PMID:39428507. |
we developed a myelin oligodendrocyte glycoprotein (mog)-specific car treg cell therapy for patients with ms. mog is expressed on the outer membrane of the myelin sheath, the insulating layer the forms around nerves, making it an ideal target for car treg therapy. |
2024-10-20 |
2024-10-23 |
mouse |
| Yan Mi, Jianjun Dong, Caiyun Liu, Qingxiang Zhang, Chao Zheng, Hao Wu, Wenrong Zhao, Jie Zhu, Zuobin Wang, Tao Ji. Amelioration of experimental autoimmune encephalomyelitis by exogenous soluble PD-L1 is associated with restraining dendritic cell maturation and CCR7-mediated migration. International immunopharmacology. vol 143. issue Pt 2. 2024-10-18. PMID:39423660. |
here, the administration of soluble pd-l1 (spd-l1) protein significantly alleviated the clinical symptoms of myelin oligodendrocyte glycoprotein (mog)-induced eae, and inhibited the expression of cluster of differentiation (cd)86, c-c motif chemokine receptor 7 (ccr7) as well as ccr7-mediated trafficking of splenic dcs, accompanied by enhancing their phagocytosis. |
2024-10-18 |
2024-10-21 |
Not clear |
| Efstratia-Maria Georgopoulou, Myrto Palkopoulou, Dimitrios Liakopoulos, Eleni Kerazi, Angelos-Michail Kalaentzis, Vanessa Barmparoussi, Michail Kokkinos, Anastasia Kaliontzoglou, Maria Anagnostoul. Myelin Oligodendrocyte Glycoprotein Antibody Disease (MOGAD)-Monophasic Optic Neuritis and Epstein-Barr Virus (EBV): A Case Report of Rare Comorbid Diagnoses in an Adolescent From a Remote Greek Island. Cureus. vol 16. issue 9. 2024-10-09. PMID:39381468. |
a unique case of a female adolescent diagnosed with myelin oligodendrocyte glycoprotein (mog) monophasic optic neuritis with epstein-barr virus (ebv) reactivation antibody profile on a remote greek island is presented, highlighting the challenges of diagnosing rare conditions in rural settings and the importance of connecting centers of expertise with regional hospitals. |
2024-10-09 |
2024-10-11 |
Not clear |