Results 91 to 100 of about 13,156 (215)

Myelitis‐Predominant Aggressive Phenotype: Unveiling Unique Patterns of Late‐Onset Neuromyelitis Optica Spectrum Disorders

open access: yesAnnals of Neurology, Volume 99, Issue 5, Page 1139-1151, May 2026.
Objective The objective of this study was to compare clinical features and prognosis of late‐onset neuromyelitis optica spectrum disorder (LO‐NMOSD, onset age ≥60 years) with adult‐onset NMOSD (AO‐NMOSD, onset age 18–59 years), and to provide insights for individualized management in elderly patients.
Ya‐Lan Pu   +15 more
wiley   +1 more source

Therapeutic decision making in autoimmune and inflammatory disorders of the central nervous system in children. [PDF]

open access: yes, 2016
Autoimmune and inflammatory disorders of the central nervous system can result in significant morbidity and mortality. Through the recognition of syndromes using diagnostic biomarkers, the clinician is now able to use immune suppressive therapies to ...
Dale, Rc, Lim, M., Nosadini, M
core   +3 more sources

Myasthenia Gravis and Neuromyelitis Optica Association

open access: yesPediatric Neurology Briefs, 2012
Investigators at the University of Oxford, UK and 8 other international neurology centers describe the clinical, serological, and temporal associations of myasthenia gravis (MG) and neuromyelitis optica spectrum disorder (NMOSD) in 16 patients.
J Gordon Millichap
doaj   +1 more source

Hypersensitivity Responses in the Central Nervous System [PDF]

open access: yes, 2015
Immune-mediated tissue damage or hypersensitivity can be mediated by autospecific IgG antibodies. Pathology results from activation of complement, and antibody-dependent cellular cytotoxicity (ADCC), mediated by inflammatory effector leukocytes include ...
Carsten Tue Berg   +5 more
core   +4 more sources

Posterior Spinal Artery Infarction With Unilateral Lumbar Spinal Cord Lesion: A Challenge in Early Diagnosis

open access: yesJournal of General and Family Medicine, Volume 27, Issue 3, May 2026.
ABSTRACT A 71‐year‐old woman presented with acute muscle weakness and paresthesia in her left lower limb with the preceding back pain and impaired deep sensation. Although initial brain and spinal MRI were normal, follow‐up spinal MRI confirmed the left‐sided posterior lesion at T10 to T12 vertebral level, leading to the diagnosis of posterior spinal ...
Munenori Iwamoto   +2 more
wiley   +1 more source

Multidisciplinary rehabilitation for adults with neuromyelitis optica spectrum disorders: A pilot study

open access: yesJournal of Rehabilitation Medicine, 2019
Objective: To provide detailed data on the effects of multidisciplinary rehabilitation for patients with neuromyelitis optica spectrum disorder with moderate to severe disability. Design: A pilot randomized control study.
Dong-Mei Suo   +9 more
doaj   +1 more source

Relapse and Neurological Prognosis in Myelin Oligodendrocyte Glycoprotein Antibody‐Associated Disease: A Retrospective Secondary Analysis of a Japanese Nationwide Epidemiologic Survey

open access: yesClinical and Experimental Neuroimmunology, Volume 17, Issue 2, May 2026.
ABSTRACT Background Some patients with myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD) experience multiple relapses and poor prognoses; however, the factors associated with these outcomes are unclear. This study aimed to identify factors associated with relapse and neurological prognosis in patients with MOGAD.
Masashi Nakamura   +4 more
wiley   +1 more source

Role of repetitive transcranial magnetic stimulation in neuromyelitis optica spectrum disorder: a case report

open access: yesThe Egyptian Journal of Neurology, Psychiatry and Neurosurgery
Background Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory disorder of the central nervous system (CNS) predominantly affecting the optic nerves and spinal cord, should be considered as a differential diagnosis in all patients ...
Noha T. Abokrysha   +6 more
doaj   +1 more source

Epidemiology, clinical presentation, radiological and laboratory features, treatment responses, and long-term outcome [PDF]

open access: yes, 2016
Background A subset of patients with neuromyelitis optica spectrum disorders (NMOSD) has been shown to be seropositive for myelin oligodendrocyte glycoprotein antibodies (MOG-IgG).
Asgari, Nasrin   +6 more
core   +1 more source

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