Category Ranking
98%
Total Visits
921
Avg Visit Duration
2 minutes
Citations
20
Article Abstract
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12049199 | PMC |
| http://dx.doi.org/10.4103/aian.aian_726_24 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
An updated, comprehensive meta-analysis of the treatment of anti-NMDAR encephalitis: Analysis, equipoise, and the urgent need for evidence over anecdote.
J Neuroimmunol
August 2025
Department of Neurology, University of Utah, Salt Lake City, UT, United States of America; George E. Wahlen Veterans Affairs Medical Center, Salt Lake City, UT, United States of America. Electronic address:
Background: There are no FDA-approved treatments for anti-N-methyl-d-aspartate receptor encephalitis (NMDARE), and no prospective, multicenter clinical trials have been completed to provide evidence for management of this disease. We evaluated changes in treatment strategies and outcomes since the previous comprehensive review in 2019.
Methods: A systematic literature review was conducted in PubMed capturing manuscripts published from January 2019 through March 2024.
Case report on severe myelin oligodendrocyte glycoprotein antibody-associated disease relapse after ectopic pregnancy and laparoscopic medical abortion: relevance of peripheral inflammation for demyelinating disease activity.
Front Immunol
May 2025
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Background: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a rare neurological condition. Tubal ectopic pregnancy is an important cause of maternal morbidity and mortality worldwide. Regular pregnancy has a disease-modifying effect on MOGAD, with an increased relapse rate postpartum.
View Article and Find Full Text PDFLongitudinally extensive transverse myelitis: Impact on functional prognosis and mortality in a 10-year follow-up cohort.
Mult Scler Relat Disord
February 2025
Neuroimmunology Group, Division of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HC-FMUSP), 255 Doutor Enéas de Carvalho Aguiar Avenue, São Paulo, 05403-000, Brazil.
Background: Neuromyelitis optica spectrum disorder (NMOSD) with positivity for aquaporin-4 antibody (AQP4-IgG) represents one of the mains etiologies of longitudinally extensive transverse myelitis (LETM). Advancements in early diagnosis and treatment have led to a decline in NMOSD-related mortality. However, long-term prognostic data for patients experiencing their first episode of LETM remain scarce, especially in Brazil.
View Article and Find Full Text PDFMOGAD and Mortality: A Rarity.
Ann Indian Acad Neurol
March 2025
Department of Pediatrics, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.
Article Synopsis
- MOGAD is usually linked to inflammation and demyelination in younger people, but this case shows it can also cause isolated encephalitis in older adults, like an 80-year-old male with cognitive issues and seizures.
- Despite normal imaging results, the patient had elevated MOG antibodies and pleocytosis in cerebrospinal fluid, pointing towards MOG antibody encephalitis.
- Treatment with intravenous immunoglobulin led to significant cognitive improvement and a reduction in antibody levels, highlighting the need for awareness of MOGAD in elderly patients to improve outcomes.