Results 31 to 40 of about 2,672,729 (207)
Multiple sclerosis or neuromyelitis optica? Re-evaluating an 18th-century illness using 21st-century software. [PDF]
In this paper we report the application of an extensive database of symptoms, signs, laboratory findings and illnesses, to the diagnosis of an historical figure.
Garrard, P, Peters, TJ
core +1 more source
Fahr’s syndrome, also known as bilateral striopallidodendate calcinosis, is a rare inherited neurodegenerative illness characterized by abnormal calcium deposition in several areas of the brain, resulting in a wide range of neuropsychological symptoms ...
Ahmad Nawaz +5 more
doaj +1 more source
Symptomatic and restorative therapies in neuromyelitis optica spectrum disorders
Neuromyelitis optica spectrum disorders (NMOSD) are a group of autoimmune inflammatory conditions that primarily target the optic nerves, spinal cord, brainstem, and occasionally the cerebrum. NMOSD is characterized by recurrent attacks of visual, motor,
Salazar-Camelo, Andrea +14 more
core +1 more source
Visual Evoked Potentials in Neuromyelitis Optica Spectrum Disorders
Background Neuromyelitis optica spectrum disorders (NMOSDs) are rare antibody-mediated disorders of the central nervous system, with a predilection for the spinal cord and optic nerves.
Otto Jesus Hernandez Fustes MD, PhD +5 more
doaj +1 more source
Neuromyelitis optica spectrum disorders (NMOSDs) are autoimmune inflammatory disorders accompanied by central nervous system damage, widespread immunemediated demyelination, and axonal damage, involving mainly the optic nerves, spinal cord, and area ...
A. N. Boyko +16 more
doaj +1 more source
N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes [PDF]
Antibodies to the N-methyl-d-aspartate subtype of glutamate receptor have been associated with a newly-described encephalopathy that has been mainly identified in young females with ovarian tumours.
Irani, Sarosh R. +27 more
core +1 more source
Status of the neuromyelitis optica spectrum disorder in Latin America
Background: Neuromyelitis optica spectrum disorders (NMOSD) is an increasing diagnostic and therapeutic challenge in Latin America (LATAM). Despite the heterogeneity of this population, ethnic and socioeconomic commonalities exist, and epidemiologic ...
Douglas Kazutoshi Sato +88 more
core +1 more source
Neuromyelitis optic spectrum disorders (NMOSD): from pathogenesis to targeted therapy
In the review, we present the main pathogenetic mechanisms of the development of neuromyelitis optic spectrum disorders (NMOSD) associated with the appearance of anti-aquaporin-4 (APQ4-IgG) autoantibodies: damage to astrocytes, including complement ...
P. A. Zaitseva, A. N. Boyko
doaj +1 more source
Late Onset of Neuromyelitis Optica Spectrum Disorders
Introduction Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune demyelinating disease of the central nervous system. NMOSD starting after the age of 50 years is considered a “late onset” (LO-NMOSD) and seems to be particularly aggressive ...
Yara Dadalti Fragoso +15 more
doaj +1 more source
Naive B cells in neuromyelitis optica spectrum disorders: impact of steroid use and relapses
Neuromyelitis optica spectrum disorders are a group of rare, but severe autoimmune diseases characterized by inflammation of the optic nerve(s) and/or spinal cord.
Janssen, Malou +13 more
core +1 more source

