Results 81 to 90 of about 6,760 (209)

Outcome and risk of recurrence in a large cohort of idiopathic longitudinally extensive transverse myelitis without AQP4/MOG antibodies

open access: yesJournal of Neuroinflammation, 2020
Background 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.
Elisabeth Maillart   +24 more
doaj   +1 more source

Cervical longitudinally extensive myelitis after vaccination with inactivated virus-based COVID-19 vaccine

open access: yesRadiology Case Reports, 2022
Myelitis, including longitudinally extensive transverse myelitis (LTEM), is reported in more than forty patients after coronavirus disease 2019 (COVID-19).
Mahsa Sepahvand, MD   +3 more
doaj   +1 more source

Mental Health and Corresponding Interventions for Persons With Physical Disabilities: A Scoping Review

open access: yesMedicine Advances, EarlyView.
This scoping review of 33 studies maps the landscape of mental health in persons with physical disabilities. It finds a high prevalence of depression, anxiety, posttraumatic stress disorder, and other psychological problems, but highlights significant heterogeneity across studies in sample size, measurement, and representativeness.
Hui Li   +7 more
wiley   +1 more source

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

open access: yesClinical 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   +2 more
wiley   +1 more source

Pediatric Acute Longitudinal Extensive Transverse Myelitis Secondary to Neuroborreliosis [PDF]

open access: yesCase Reports in Neurology, 2015
Lyme neuroborreliosis has several different clinical manifestations in children, of which facial nerve palsies, meningitis and radiculopathies are the most common. Transverse myelitis (TM) secondary to Lyme disease has been reported in rare occasions, typically presenting with severe weakness, sensory abnormalities and autonomic dysfunction. We present
Sana Khan   +3 more
openaire   +3 more sources

Novel Glial Targets and Recurrent Longitudinally Extensive Transverse Myelitis [PDF]

open access: yesJAMA Neurology, 2018
This cohort study presents serological data with regard to 2 novel glial targets (myelin oligodendrocyte glycoprotein and glial fibrillary acidic protein) in recurrent longitudinally extensive transverse myelitis.
Jiraporn, Jitprapaikulsan   +6 more
openaire   +2 more sources

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

open access: yesFrontiers 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   +5 more
doaj   +1 more source

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

open access: yesFrontiers 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   +3 more
doaj   +1 more source

Integrated Blood Inflammatory Ratios and Cerebrospinal Fluid Blood‒Brain Barrier Dysfunction Predict Relapse Risk in Neuromyelitis Optica Spectrum Disorder

open access: yesBrain and Behavior, Volume 16, Issue 6, June 2026.
ABSTRACT Background Relapse is the primary driver of irreversible disability accumulation in neuromyelitis optica spectrum disorder (NMOSD). Although aquaporin‐4 immunoglobulin G (AQP4‐IgG) is central to disease diagnosis and pathogenesis, reliable tools for individualized relapse risk stratification remain limited.
Xingyue Zheng   +11 more
wiley   +1 more source

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

open access: yesNeurology 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

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