Results 71 to 80 of about 7,096 (184)
Demyelinating syndrome in SLE: review of different disease subtypes and report of a case series
Demyelinating syndrome (DS) is a rare manifestation of systemic lupus erythematosus (SLE) (1%) with high clinical heterogeneity and potentially severe prognosis. It can represent a diagnostic and therapeutic challenge for clinicians.
E. Chessa +4 more
doaj +1 more source
ABSTRACT There is a need to better understand the indications and safety profiles for therapeutic plasma exchange (TPE) in children. We aimed to assess pediatric TPE practice at a large academic center by retrospective chart review from 2011 to 2022. Patient demographics and clinical information including American Society for Apheresis (ASFA) category ...
Benjamin C. Lee +4 more
wiley +1 more source
Neuro-ophthalmic manifestation of neuromyelitis optica spectrum disorders
Neuromyelitis optica spectrum disorders (NMOSDs) include classic neuromyelitis optica (NMO), opticospinal multiple sclerosis (OSMS), limited form of NMO and isolated optic neuritis or myelitis accompanied by either systemic autoimmune diseases or ...
Xiao-jun ZHANG, Xian-hao XU
doaj
Pain in patients with neuromyelitis optica spectrum disorders
Neuromyelitis optica spectrum disorders (NMOSD) are a group of chronic autoimmune diseases of the central nervous system with a relapsing course. Unfortunately, the symptoms of exacerbation cannot always be completely stopped, and in addition to motor ...
E. S. Novikova, A. S. Kotov, S. V. Kotov
doaj +1 more source
ABSTRACT Purpose Spontaneous reporting of a possible link between myelin oligodendrocyte glycoprotein (MOG) antibody‐associated disease (MOGAD) and mRNA SARS‐CoV‐2 vaccination warrants further examination. Hence, the objective of this study was to investigate the association between MOG‐IgG positivity as a proxy for MOGAD and mRNA SARS‐CoV‐2 ...
Tine Iskov Kopp +9 more
wiley +1 more source
Pain in AQP4-IgG-positive and MOG-IgG-positive neuromyelitis optica spectrum disorders
Background Pain is a frequent symptom in aquaporin-4-immunoglobulin-G-positive neuromyelitis optica spectrum disorders (AQP4-IgG-pos. NMOSD). Data on pain in myelin-oligodendrocyte-glycoprotein-immunoglobulin-G autoimmunity with a clinical NMOSD ...
Susanna Asseyer +7 more
doaj +1 more source
Annals of Clinical and Translational Neurology, Volume 13, Issue 6, Page 1303-1304, June 2026.
Lea Gerischer +3 more
wiley +1 more source
Income growth was significantly lower for people with MS compared to controls, and men with MS lost income at a younger age than women with MS (49 vs. 55 years). Men also lost income earlier in the disease course than women (2 vs. 5 years post‐diagnosis).
Anne Høgset +6 more
wiley +1 more source
Neuromyelitis optica spectrum disorders (NMOSDs) is a new concept which includes classical neuromyelitis optica (NMO) and partial forms of NMO such as recurrent optic neuritis with positive aquaporin-4 antibodies (AQP4) or brainstem symptoms (intractable
Nicolas Collongues, Jérôme de Seze
doaj +1 more source
Update on neuromyelitis optica: natural history and management
Panitha Jindahra1,2, Gordon T Plant1,21The National Hospital for Neurology and Neurosurgery, Queen Square, London, UK; 2St Thomas' Hospital, Westminster Bridge Road, London, UKAbstract: Neuromyelitis optica or Devic disease is an inflammatory ...
Jindahra P, Plant GT
doaj

