Results 81 to 90 of about 1,878,367 (184)

Neuromyelitis Optica Spectrum Disorder with Tumefactive Demyelination mimicking Multiple Sclerosis: a rare case

Frontiers in Neurology, 2016
Neuromyelitis optica spectrum disorder (NMOSD) is a diverse condition which not only encompasses isolated longitudinally extensive transverse myelitis and optic neuritis but also includes area postrema syndrome, acute brainstem syndrome, symptomatic ...
UJJAWAL eROY, Dinesh eSatyanarayan, Koushik ePan, Alak ePandit, Goutam eGanguly, Ajay ePanwar   +5 more
doaj   +1 more source

Cryptococcal infection causing longitudinal extensive transverse myelitis in an immunocompetent individual: Case report and literature review

Frontiers in Neurology, 2023
Cryptococcal CNS infections in immunocompetent individuals are occasionally reported in literature. The spinal manifestations of cryptococcal CNS infections are epidural abscess, chronic arachnoiditis, intramedullary granuloma, myelitis and vasculitis ...
Ashwin Kumar Panda, Sourav Hazra, Aldrin Anthony, Suman Kushwaha   +3 more
doaj   +1 more source

A Rare Overlap of AQP4 and MOG Seropositivity in Neuromyelitis Optica Spectrum Disorder: A Case Report

Clinical and Experimental Neuroimmunology, Volume 17, Issue 3, August 2026.
ABSTRACT Background Neuromyelitis optica spectrum disorder (NMOSD) is an immune‐mediated disorder of the central nervous system associated with autoantibodies against aquaporin‐4 (AQP4). This is distinct from myelin‐oligodendrocyte glycoprotein antibody‐associated disease (MOGAD), defined by anti‐MOG antibodies.
Sarah E. Butler, Siew Kar Chen, Mastura Monif   +2 more
wiley   +1 more source

Longitudinal extensive transverse myelitis due to tuberculosis

Journal of Postgraduate Medicine, 2014
Tuberculosis of the central nervous system (CNS) accounts for approximately 1% of all cases of tuberculosis and half of these involve the spine. Intramedullary involvement is rare in tuberculosis and usually present in the form of radiculomyelitis, transverse myelitis, intraspinal granulomas, or thrombosis of anterior spinal ...
S K, Sahu, S, Giri, N, Gupta
openaire   +2 more sources

Correction to: Abstracts from the 5th International Porto Congress of Multiple Sclerosis

Neurology and Therapy, 2019
The given name of one of the authors was incorrectly published as Vera in abstract EPIII028 “Anti-MOG Antibody-Positive Isolated Longitudinally Extensive Transverse Myelitis”. The correct name should read as follows:
Maria José Sá
doaj   +1 more source

Update on the Incidence of Paediatric Multiple Sclerosis, Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease, Aquaporin‐4 Antibody–Positive Neuromyelitis Optica Spectrum Disorder, and Other Acquired Demyelinating Syndromes in the Netherlands, 2017–2025, Including the COVID‐19 Pandemic

European Journal of Neurology, Volume 33, Issue 8, August 2026.
ABSTRACT Background Acquired demyelinating syndromes (ADS) in children include multiple sclerosis (MS), myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD), aquaporin 4 antibody‐positive neuromyelitis optica spectrum disorder (AQP4+ NMOSD), and other seronegative disorders.
Sandy Molenaar, Michiel S. J. Buijze, Arlette L. Bruijstens, Yu Yi M. Wong, Maud A. Quist, C. Louk de Mol, Beatrijs H. A. Wokke, Rinze F. Neuteboom, Dutch Study Group for Paediatric Multiple Sclerosis and Acute Disseminated Encephalomyelitis   +8 more
wiley   +1 more source

Longitudinally extensive transverse myelitis with pulmonary tuberculosis

Medicine, 2018
Longitudinally extensive transverse myelitis (LETM) is characterized by contiguous inflammatory lesions of spinal cord extending to ≥3 vertebral segments. The etiology of LETM is complicated, including various infection, autoimmune disease, and so on. Neuromyelitis optic spectrum disorder (NMOSD) is the most common cause of LETM.
Zhang, Yu, Zhu, Mingqin, Wang, Lifang, Shi, Miao, Deng, Hui   +4 more
openaire   +2 more sources

Spinal Cord Infarction Versus Idiopathic Transverse Myelitis: Clinical, Radiological, and Functional Insights From a Retrospective Cohort Study

Annals of Clinical and Translational Neurology, Volume 13, Issue 7, Page 1388-1397, July 2026.
ABSTRACT Introduction Spinal cord infarction (SCI) is a rare but devastating myelopathy, characterized by a high disability rate and an unfavorable prognosis. It has often been underdiagnosed and misdiagnosed as idiopathic transverse myelitis (ITM). This study aimed to describe the clinical features, radiological biomarkers, treatments, and functional ...
Zeqiang Ji, Jianlong Zhang, Yiming Shi, Shiyu Shan, Yang Du, Guangshuo Li, Ying Jin, Yani Zhang, Chuanying Wang, Yijun Lin, Yuhao Guo, Decai Tian, Xingquan Zhao, Tian Song   +13 more
wiley   +1 more source

Safety considerations of gene‐based therapies for Alzheimer's disease

Alzheimer's &Dementia, Volume 22, Issue 7, July 2026.
Abstract Gene‐based therapies show increasing promise for the treatment of neurologic disease. In 2016, nusinersen, an RNA‐based therapy, was approved for children with spinal muscular atrophy (SMA). Over 200 clinical trials have utilized gene therapy approaches for a host of neurodegenerative and neuromuscular disorders, including Alzheimer's disease (
Elizabeth A. Bevins, Gabriel C. Léger, Michelle A. Herman, John M. Ringman, Subhojit Roy, Matthew Shtrahman, Judy Pa, Howard H. Feldman   +7 more
wiley   +1 more source

Longitudinally extensive transverse myelitis with anti-myelin oligodendrocyte glycoprotein antibodies following SARS-CoV-2 infection

, 2021
© 2021 Elsevier B.V. All rights reserved.We report the case of a patient with symptoms of myelopathy following acute SARS-CoV-2 infection. MRI documented a longitudinally extensive transverse myelitis and further investigation was unremarkable with the ...
Leal Rato, Miguel, Dias Da Costa, Mariana, Cruz, Diana, Antunes, Ana Patrícia, Albuquerque, Luísa, Valadas, Anabela   +5 more
core   +1 more source