| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Shripad S Pujari, Rahul V Kulkarni, Dattatraya B Nadgir, Pawan K Ojha, Shashank Nagendra, Vikram Aglave, Rashmi D Nadgir, Hemant Sant, Nilesh Palasdeokar, Satish Nirhale, Sunil Bandisht. Myelin Oligodendrocyte Glycoprotein (MOG)-IgG Associated Demyelinating Disease: Our Experience with this Distinct Syndrome. Annals of Indian Academy of Neurology. vol 24. issue 1. 2021-04-30. PMID:33911382. |
myelin oligodendrocyte glycoprotein (mog)-igg associated demyelinating disease: our experience with this distinct syndrome. |
2021-04-30 |
2023-08-13 |
Not clear |
| Shripad S Pujari, Rahul V Kulkarni, Dattatraya B Nadgir, Pawan K Ojha, Shashank Nagendra, Vikram Aglave, Rashmi D Nadgir, Hemant Sant, Nilesh Palasdeokar, Satish Nirhale, Sunil Bandisht. Myelin Oligodendrocyte Glycoprotein (MOG)-IgG Associated Demyelinating Disease: Our Experience with this Distinct Syndrome. Annals of Indian Academy of Neurology. vol 24. issue 1. 2021-04-30. PMID:33911382. |
discovery of serum myelin oligodendrocyte glycoprotein (mog) antibody testing in demyelination segregated mog-igg disease from aq-4-igg positive nmosd. |
2021-04-30 |
2023-08-13 |
Not clear |
| Archana Khan, Hiren Panwala, Divya Ramadoss, Raju Khubchandan. Myelin Oligodendrocyte Glycoprotein (MOG) Antibody Disease in a 11 Year Old with COVID-19 Infection. Indian journal of pediatrics. vol 88. issue 5. 2021-04-28. PMID:33471314. |
myelin oligodendrocyte glycoprotein (mog) antibody disease in a 11 year old with covid-19 infection. |
2021-04-28 |
2023-08-13 |
Not clear |
| Gwyneth Zai, Paul D Arnold, Margaret A Richter, Gregory L Hanna, David Rosenberg, James L Kenned. An association of Myelin Oligodendrocyte Glycoprotein (MOG) gene variants with white matter volume in pediatric obsessive-compulsive disorder. Psychiatry research. Neuroimaging. vol 307. 2021-04-27. PMID:33302097. |
an association of myelin oligodendrocyte glycoprotein (mog) gene variants with white matter volume in pediatric obsessive-compulsive disorder. |
2021-04-27 |
2023-08-13 |
Not clear |
| Gwyneth Zai, Paul D Arnold, Margaret A Richter, Gregory L Hanna, David Rosenberg, James L Kenned. An association of Myelin Oligodendrocyte Glycoprotein (MOG) gene variants with white matter volume in pediatric obsessive-compulsive disorder. Psychiatry research. Neuroimaging. vol 307. 2021-04-27. PMID:33302097. |
the myelin oligodendrocyte glycoprotein (mog) gene plays a major role in myelination, and has previously demonstrated significant association with this disorder, thus variations in this gene may contribute to observed white matter alterations. |
2021-04-27 |
2023-08-13 |
Not clear |
| Fernanda Veloso Pereira, Vinícius de Menezes Jarry, José Thiago Souza Castro, Simone Appenzeller, Fabiano Rei. Pediatric inflammatory demyelinating disorders and mimickers: How to differentiate with MRI? Autoimmunity reviews. vol 20. issue 5. 2021-04-20. PMID:33727154. |
the main imaging patterns of pediatric inflammatory demyelinating disorders and mimicking entities, including multiple sclerosis, neuromyelitis optica spectrum disorders, acute disseminated encephalomyelitis, mog (myelin oligodendrocyte glycoprotein) antibody-related disorders and differential diagnoses will be addressed in this article, highlighting key points to the differential diagnosis. |
2021-04-20 |
2023-08-13 |
Not clear |
| Tianrong Yeo, Giordani Rodrigues Dos Passos, Louwai Muhammed, Rosie Everett, Sandra Reeve, Silvia Messina, Fay Probert, Maria Isabel Leite, Jacqueline Palac. Factors associated with fatigue in CNS inflammatory diseases with AQP4 and MOG antibodies. Annals of clinical and translational neurology. vol 7. issue 3. 2021-04-12. PMID:32187851. |
fatigue is a common and disabling symptom amongst people with multiple sclerosis, however it has not been compared across the central nervous system (cns) inflammatory diseases associated with aquaporin-4 (aqp4) and myelin oligodendrocyte glycoprotein (mog) antibodies (ab). |
2021-04-12 |
2023-08-13 |
Not clear |
| Orhan Aktas, Tania Kümpfe. [From neuromyelitis optica to neuromyelitis optica spectrum disorder: from clinical syndrome to diagnistic classification]. Der Nervenarzt. vol 92. issue 4. 2021-04-09. PMID:33728474. |
a subset of aqp4-igg negative nmosd patients have been found to harbor autoantibodies targeting myelin oligodendrocyte glycoprotein (mog), which is considered as a distinct disease entity: these mog antibody-associated disorders (mogad) can present with clinical syndromes resembling both nmosd and ms and are currently the subject of intensive research. |
2021-04-09 |
2023-08-13 |
human |
| Sven Jarius, Brigitte Wildeman. [Aquaporin 4 antibody-positive neuromyelitis optica spectrum disorders and myelin oligodendrocyte glycoprotein antibody-associated encephalomyelitis. A brief review]. Der Nervenarzt. vol 92. issue 4. 2021-04-09. PMID:33787942. |
aquaporin 4 (aqp4) immunoglobulin (ig)g-associated neuromyelitis optica spectrum disorders (nmosd) and myelin oligodendrocyte glycoprotein immunoglobulin (ig)g-associated encephalomyelitis (mog-em, also termed mog antibody-associated disease, mogad) are important autoimmune differential diagnoses of multiple sclerosis (ms), which differ from ms with respect to optimum treatment and prognosis. |
2021-04-09 |
2023-08-13 |
Not clear |
| Tai Otani, Takashi Irioka, Susumu Igarashi, Kimihiko Kaneko, Toshiyuki Takahashi, Takanori Yokot. Self-remitting cerebral cortical encephalitis associated with myelin oligodendrocyte glycoprotein antibody mimicking acute viral encephalitis: A case report. Multiple sclerosis and related disorders. vol 41. 2021-03-29. PMID:32146429. |
afterwards, the characteristic brain mri findings required us to check the patient's serum, and the final diagnosis of myelin oligodendrocyte glycoprotein (mog) antibody-positive cerebral cortical encephalitis (cce) was confirmed. |
2021-03-29 |
2023-08-13 |
Not clear |
| Madina Tugizova, Haojun Feng, Anna Tomczak, Kristen Steenerson, May Ha. Case series: Hearing loss in neuromyelitis optica spectrum disorders. Multiple sclerosis and related disorders. vol 41. 2021-03-29. PMID:32155460. |
aquaporin 4 (aqp4)- and myelin oligodendrocyte glycoprotein (mog)-associated neuromyelitis optica spectrum disorders (nmosd) are thought to primarily affect the central nervous system (cns). |
2021-03-29 |
2023-08-13 |
Not clear |
| Saori Kawakami, Satoshi Akamine, Pin Fee Chong, Fumiya Yamashita, Kenichi Maeda, Toshiyuki Takahashi, Ryutaro Kir. Isolated cranial neuritis of the oculomotor nerve: Expanding the MOG phenotype? Multiple sclerosis and related disorders. vol 41. 2021-03-29. PMID:32182468. |
autoantibody against myelin oligodendrocyte glycoprotein (mog) has been reported in a range of demyelinating neurological entities. |
2021-03-29 |
2023-08-13 |
Not clear |
| Ke Li, Yajing Zhan, Xiangmin She. Multiple intracranial lesions with lung adenocarcinoma: A rare case of MOG-IgG-associated encephalomyelitis. Multiple sclerosis and related disorders. vol 42. 2021-03-29. PMID:32234600. |
myelin oligodendrocyte glycoprotein (mog) is an important marker on the surface of oligodendrocytes and is associated with many demyelinating diseases. |
2021-03-29 |
2023-08-13 |
Not clear |
| Chi Hou, Wenlin Wu, Yang Tian, Yani Zhang, Haixia Zhu, Yiru Zeng, Bingwei Peng, Kelu Zheng, Xiaojing Li, Wenxiong Che. Clinical analysis of anti-NMDAR encephalitis combined with MOG antibody in children. Multiple sclerosis and related disorders. vol 42. 2021-03-29. PMID:32234601. |
to analyze the clinical features in children with anti-nmdar encephalitis combined with myelin oligodendrocyte glycoprotein antibody (mog ab). |
2021-03-29 |
2023-08-13 |
Not clear |
| Athanasios Papathanasiou, Jing-Ming Yeo, Miles Humberstone, Akram A Hossein. MOG-antibody-associated hypertrophic pachymeningitis. Multiple sclerosis and related disorders. vol 42. 2021-03-29. PMID:32361264. |
the clinical spectrum of myelin oligodendrocyte glycoprotein (mog)-antibody-associated disease is expanding. |
2021-03-29 |
2023-08-13 |
Not clear |
| Joyutpal Das, Atta Gill, Christine Lo, Natalie Chan-Lam, Siân Price, Stephen B Wharton, Helen Jessop, Basil Sharrack, John A Snowde. A Case of Multiple Sclerosis-Like Relapsing Remitting Encephalomyelitis Following Allogeneic Hematopoietic Stem Cell Transplantation and a Review of the Published Literature. Frontiers in immunology. vol 11. 2021-03-29. PMID:32431694. |
neuromyelitis optica (nmo) and myelin oligodendrocyte glycoprotein (mog) antibodies were negative. |
2021-03-29 |
2023-08-13 |
Not clear |
| Satoru Tanaka, Baku Hashimoto, Shoko Izaki, Satoru Oji, Hikoaki Fukaura, Kyoichi Nomur. Clinical and immunological differences between MOG associated disease and anti AQP4 antibody-positive neuromyelitis optica spectrum disorders: Blood-brain barrier breakdown and peripheral plasmablasts. Multiple sclerosis and related disorders. vol 41. 2021-03-22. PMID:32114369. |
patients with anti-aquaporin-4 (aqp4) water channel antibody-positive neuromyelitis optica spectrum disorders (aqp4-nmosd) and myelin oligodendrocyte glycoprotein (mog) associated disease (mogad) often present with similar clinical symptoms, and some cases are hard to differentiate at the time of onset. |
2021-03-22 |
2023-08-13 |
Not clear |
| Thomas Foiadelli, Matteo Gastaldi, Silvia Scaranzin, Diego Franciotta, Salvatore Savast. Seizures and myelin oligodendrocyte glycoprotein (MOG) antibodies: Two paradigmatic cases and a review of the literature. Multiple sclerosis and related disorders. vol 41. 2021-03-22. PMID:32163756. |
seizures and myelin oligodendrocyte glycoprotein (mog) antibodies: two paradigmatic cases and a review of the literature. |
2021-03-22 |
2023-08-13 |
Not clear |
| Thomas Foiadelli, Matteo Gastaldi, Silvia Scaranzin, Diego Franciotta, Salvatore Savast. Seizures and myelin oligodendrocyte glycoprotein (MOG) antibodies: Two paradigmatic cases and a review of the literature. Multiple sclerosis and related disorders. vol 41. 2021-03-22. PMID:32163756. |
myelin oligodendrocyte glycoprotein (mog) antibodies (abs) have been associated with a heterogeneous range of acquired cns demyelinating disorders. |
2021-03-22 |
2023-08-13 |
Not clear |
| Elisabeth Maillart, Françoise Durand-Dubief, Céline Louapre, Bertrand Audoin, Bertrand Bourre, Nathalie Derache, Jonathan Ciron, Nicolas Collongues, Jérome de Sèze, Mikael Cohen, Christine Lebrun-Frenay, Nawel Hadhoum, Hélène Zéphir, Romain Deschamps, Clarisse Carra-Dallière, Pierre Labauge, Philippe Kerschen, Alexis Montcuquet, Sandrine Wiertlewski, David Laplaud, Gwenaëlle Runavot, Sandra Vukusic, Caroline Papeix, Romain Marignie. Outcome and risk of recurrence in a large cohort of idiopathic longitudinally extensive transverse myelitis without AQP4/MOG antibodies. Journal of neuroinflammation. vol 17. issue 1. 2021-03-18. PMID:32326965. |
longitudinally extensive transverse myelitis (letm) is classically related to aquaporin (aqp4)-antibodies (ab) neuromyelitis optica spectrum disorders (nmosd) or more recently to myelin oligodendrocyte glycoprotein (mog)-ab associated disease. |
2021-03-18 |
2023-08-13 |
Not clear |