| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Ying Peng, Lei Liu, Yuanchu Zheng, Zhixin Qiao, Kai Feng, Jiawei Wan. Diagnostic implications of MOG/AQP4 antibodies in recurrent optic neuritis. Experimental and therapeutic medicine. vol 16. issue 2. 2020-09-30. PMID:30112048. |
the present study aimed to detect myelin oligodendrocyte glycoprotein (mog) and aquaporin-4 (aqp4) antibodies in serum specimens of patients with recurrent optic neuritis (ron) through establishing 293 cells with stable expression of mog and the complete genomic sequence as the substrate using a cell-based assay (cba). |
2020-09-30 |
2023-08-13 |
Not clear |
| Ying Peng, Lei Liu, Yuanchu Zheng, Zhixin Qiao, Kai Feng, Jiawei Wan. Diagnostic implications of MOG/AQP4 antibodies in recurrent optic neuritis. Experimental and therapeutic medicine. vol 16. issue 2. 2020-09-30. PMID:30112048. |
furthermore, the clinical features of mog antibody-positive recurrent optic neuritis (mog-ron) were assessed. |
2020-09-30 |
2023-08-13 |
Not clear |
| Hadas Stiebel-Kalish, Mark Andrew Hellmann, Michael Mimouni, Friedemann Paul, Omer Bialer, Michael Bach, Itay Lota. Does time equal vision in the acute treatment of a cohort of AQP4 and MOG optic neuritis? Neurology(R) neuroimmunology & neuroinflammation. vol 6. issue 4. 2020-09-30. PMID:31355308. |
does time equal vision in the acute treatment of a cohort of aqp4 and mog optic neuritis? |
2020-09-30 |
2023-08-13 |
Not clear |
| Shunichiro Takano, Aya Hanabusa, Yuji Yoshikawa, Kaori Sassa, Airi Shimura, Takuhei Shoji, Hisao Ohde, Kei Shinoda, Hideo Yamanouch. Pattern Visually Evoked Potentials in Japanese Girl With Optic Neuritis and Seropositive to Anti-myelin Oligodendrocyte Glycoprotein (MOG) Antibody. Frontiers in neurology. vol 10. 2020-09-30. PMID:31920953. |
pattern visually evoked potentials in japanese girl with optic neuritis and seropositive to anti-myelin oligodendrocyte glycoprotein (mog) antibody. |
2020-09-30 |
2023-08-13 |
Not clear |
| Sonja Hochmeister, Thomas Gattringer, Martin Asslaber, Verena Stangl, Michaela Tanja Haindl, Christian Enzinger, Romana Höftberge. A Fulminant Case of Demyelinating Encephalitis With Extensive Cortical Involvement Associated With Anti-MOG Antibodies. Frontiers in neurology. vol 11. 2020-09-28. PMID:32117004. |
anti-myelin oligodendrocyte glycoprotein (mog) antibodies (mog-abs) are commonly associated with clinical presentations as acute disseminated encephalomyelitis (adem) in both adults and children and anti-aquaporin 4 antibody-seronegative neuromyelitis optica spectrum disorder (nmosd) and related syndromes such as optic neuritis, myelitis, and brainstem encephalitis. |
2020-09-28 |
2023-08-13 |
Not clear |
| Pranjal Gupta, Vinay Goyal, Achal Kumar Srivastava, Awadh Kishor Pandit, Kameshwar Prasa. Uveitis, optic neuritis and MOG. Multiple sclerosis journal - experimental, translational and clinical. vol 6. issue 2. 2020-09-28. PMID:32489673. |
uveitis, optic neuritis and mog. |
2020-09-28 |
2023-08-13 |
Not clear |
| S Ramanathan, C Fraser, S R Curnow, M Ghaly, R J Leventer, J Lechner-Scott, A Henderson, S Reddel, R C Dale, F Brilo. Uveitis and optic perineuritis in the context of myelin oligodendrocyte glycoprotein antibody seropositivity. European journal of neurology. vol 26. issue 8. 2020-08-07. PMID:30748058. |
antibodies to myelin oligodendrocyte glycoprotein (mog) have been identified in both children and adults with demyelination, with a strong association with bilateral or recurrent optic neuritis (on). |
2020-08-07 |
2023-08-13 |
Not clear |
| Carlos A Pérez, Paunel Agyei, Bhanu Gogia, Rebecca Harrison, Rohini Samudralwa. Overlapping autoimmune syndrome: A case of concomitant anti-NMDAR encephalitis and myelin oligodendrocyte glycoprotein (MOG) antibody disease. Journal of neuroimmunology. vol 339. 2020-07-09. PMID:31837635. |
antibodies against myelin oligodendrocyte glycoprotein (mog) are associated with a range of clinical presentations including acute disseminated encephalomyelitis (adem), optic neuritis, and transverse myelitis. |
2020-07-09 |
2023-08-13 |
Not clear |
| Ilijas Jelcic, James V M Hanson, Sebastian Lukas, Konrad P Weber, Klara Landau, Misha Pless, Markus Reindl, Michael Weller, Roland Martin, Andreas Lutterotti, Sven Schipplin. Unfavorable Structural and Functional Outcomes in Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis. Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society. vol 39. issue 1. 2020-06-15. PMID:30015656. |
recurrent optic neuritis (ron) associated with myelin oligodendrocyte glycoprotein (mog)-specific antibodies has been initially reported to show a better clinical outcome than aquaporin-4 (aqp4)-seropositive on in neuromyelitis optica spectrum disorder (nmosd). |
2020-06-15 |
2023-08-13 |
Not clear |
| Deena A Tajfirouz, M Tariq Bhatti, John J Che. Clinical Characteristics and Treatment of MOG-IgG-Associated Optic Neuritis. Current neurology and neuroscience reports. vol 19. issue 12. 2020-06-09. PMID:31773369. |
antibodies against myelin oligodendrocyte glycoprotein (mog) are associated with a unique acquired central nervous system demyelinating disease-termed mog-igg-associated disorder (mogad)-which has a variety of clinical manifestations, including optic neuritis, transverse myelitis, acute disseminating encephalomyelitis, and brainstem encephalitis. |
2020-06-09 |
2023-08-13 |
Not clear |
| Ünsal Yılmaz, Selvinaz Edizer, Çisel Yazan Songür, Yiğithan Güzin, Fatma Sibel Dura. Atypical presentation of MOG-related disease: Slowly progressive behavioral and personality changes following a seizure. Multiple sclerosis and related disorders. vol 36. 2020-06-08. PMID:31525625. |
myelin oligodendrocyte glycoprotein (mog) antibodies-related disease is mainly presented with acute disseminated encephalomyelitis (adem), recurrent optic neuritis, and neuromyelitis optica spectrum disorders (nmosds), however the complete clinical spectrum has not yet been defined. |
2020-06-08 |
2023-08-13 |
Not clear |
| Thea Giacomini, Thomas Foiadelli, Pietro Annovazzi, Margherita Nosadini, Matteo Gastaldi, Diego Franciotta, Claudio Panarese, Paolo Capris, Paola Camicione, Paola Lanteri, Elisa De Grandis, Giulia Prato, Ramona Cordani, Lino Nobili, Giovanni Morana, Andrea Rossi, Angela Pistorio, Maria Cellerino, Antonio Uccelli, Stefano Sartori, Salvatore Savasta, Maria Margherita Mancard. Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients. Multiple sclerosis and related disorders. vol 39. 2020-04-27. PMID:31896061. |
pediatric optic neuritis and anti mog antibodies: a cohort of italian patients. |
2020-04-27 |
2023-08-13 |
Not clear |
| Thea Giacomini, Thomas Foiadelli, Pietro Annovazzi, Margherita Nosadini, Matteo Gastaldi, Diego Franciotta, Claudio Panarese, Paolo Capris, Paola Camicione, Paola Lanteri, Elisa De Grandis, Giulia Prato, Ramona Cordani, Lino Nobili, Giovanni Morana, Andrea Rossi, Angela Pistorio, Maria Cellerino, Antonio Uccelli, Stefano Sartori, Salvatore Savasta, Maria Margherita Mancard. Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients. Multiple sclerosis and related disorders. vol 39. 2020-04-27. PMID:31896061. |
recent studies reported that anti myelin oligodendrocyte glycoprotein (mog) antibody (ab) related optic neuritis (on) tend to have characteristics that differ from seronegative ones. |
2020-04-27 |
2023-08-13 |
Not clear |
| Bojan Rojc, Barbara Podnar, Francesc Grau. A case of recurrent MOG antibody positive bilateral optic neuritis and anti-NMDAR encephalitis: Different biological evolution of the two associated antibodies. Journal of neuroimmunology. vol 328. 2019-11-29. PMID:30599296. |
a case of recurrent mog antibody positive bilateral optic neuritis and anti-nmdar encephalitis: different biological evolution of the two associated antibodies. |
2019-11-29 |
2023-08-13 |
Not clear |
| Patrick Peschl, Monika Bradl, Romana Höftberger, Thomas Berger, Markus Reind. Myelin Oligodendrocyte Glycoprotein: Deciphering a Target in Inflammatory Demyelinating Diseases. Frontiers in immunology. vol 8. 2019-11-20. PMID:28533781. |
using cell-based assays with recombinant full-length, conformationally intact mog, several recent studies have revealed that mog abs can be found in a subset of predominantly pediatric patients with acute disseminated encephalomyelitis (adem), aquaporin-4 (aqp4) seronegative neuromyelitis optica spectrum disorders (nmosd), monophasic or recurrent isolated optic neuritis (on), or transverse myelitis, in atypical ms and in |
2019-11-20 |
2023-08-13 |
human |
| Itay Lotan, Mark A Hellmann, Felix Benninger, Hadas Stiebel-Kalish, Israel Steine. Recurrent optic neuritis - Different patterns in multiple sclerosis, neuromyelitis optica spectrum disorders and MOG-antibody disease. Journal of neuroimmunology. vol 324. 2019-10-03. PMID:30267996. |
optic neuritis is a frequent finding in multiple sclerosis (ms) and in neuromyelitis optica spectrum disorder (nmosd), as well as in myelin-oligodendrocyte glycoprotein (mog) -positive disease. |
2019-10-03 |
2023-08-13 |
Not clear |
| Anjiao Peng, Masako Kinoshita, Wanlin Lai, Arui Tan, Xiangmiao Qiu, Lin Zhang, Wanling Li, Lei Che. Retinal nerve fiber layer thickness in optic neuritis with MOG antibodies: A systematic review and meta-analysis. Journal of neuroimmunology. vol 325. 2019-10-03. PMID:30290966. |
retinal nerve fiber layer thickness in optic neuritis with mog antibodies: a systematic review and meta-analysis. |
2019-10-03 |
2023-08-13 |
Not clear |
| John J Chen, W Oliver Tobin, Masoud Majed, Jiraporn Jitprapaikulsan, James P Fryer, Jacqueline A Leavitt, Eoin P Flanagan, Andrew McKeon, Sean J Pittoc. Prevalence of Myelin Oligodendrocyte Glycoprotein and Aquaporin-4-IgG in Patients in the Optic Neuritis Treatment Trial. JAMA ophthalmology. vol 136. issue 4. 2019-09-12. PMID:29470571. |
autoantibodies to aquaporin-4 (aqp4) and myelin oligodendrocyte glycoprotein (mog) are recently established biomarkers of autoimmune optic neuritis whose frequency and accompanying phenotype, especially for mog-igg, are still being characterized. |
2019-09-12 |
2023-08-13 |
Not clear |
| Jiraporn Jitprapaikulsan, John J Chen, Eoin P Flanagan, W Oliver Tobin, Jim P Fryer, Brian G Weinshenker, Andrew McKeon, Vanda A Lennon, Jacqueline A Leavitt, Jan-Mendelt Tillema, Claudia Lucchinetti, B Mark Keegan, Orhun Kantarci, Cheryl Khanna, Sarah M Jenkins, Grant M Spears, Jessica Sagan, Sean J Pittoc. Aquaporin-4 and Myelin Oligodendrocyte Glycoprotein Autoantibody Status Predict Outcome of Recurrent Optic Neuritis. Ophthalmology. vol 125. issue 10. 2019-09-05. PMID:29716788. |
to determine the aquaporin-4 and myelin oligodendrocyte glycoprotein (mog) immunoglobulin g (igg) serostatus and visual outcomes in patients with recurrent optic neuritis (ron) initially seeking treatment. |
2019-09-05 |
2023-08-13 |
Not clear |
| Sudarshini Ramanathan, Gina L O'grady, Stephen Malone, Claire G Spooner, David A Brown, Deepak Gill, Fabienne Brilot, Russell C Dal. Isolated seizures during the first episode of relapsing myelin oligodendrocyte glycoprotein antibody-associated demyelination in children. Developmental medicine and child neurology. vol 61. issue 5. 2019-08-26. PMID:30221764. |
myelin oligodendrocyte glycoprotein (mog) antibodies have a strong association with acute disseminated encephalomyelitis (adem) in children, and bilateral and recurrent optic neuritis in children and adults. |
2019-08-26 |
2023-08-13 |
Not clear |