Results 71 to 80 of about 18,389 (170)
Tumefactive demyelinating lesions (TDL) represent a diagnostic dilemma for clinicians, and in rare atypical cases a collaboration of a neuroradiologist, a neurologist, and a neuropathologist is warranted for accurate diagnosis.
Maria-Evgenia Brinia (12241238) +5 more
core +1 more source
Factors for Rituximab Refractoriness in AQP4‐IgG+ NMOSD: A Cohort Study
ABSTRACT Objective Neuromyelitis optica spectrum disorder (NMOSD) is a severe autoimmune condition of the central nervous system (CNS), often associated with aquaporin‐4 antibodies (AQP4‐IgG). Rituximab, a CD20+ B‐cell depleting monoclonal antibody, is widely used as first‐line therapy.
Mariano Marrodan +8 more
wiley +1 more source
Value of 18F-FET PET in Patients With Suspected Tumefactive Demyelinating Disease-Preliminary Experience From a Retrospective Analysis [PDF]
PURPOSE To investigate the diagnostic value of F-fluoroethyl-L-tyrosine (FET) positron emission tomography (PET) in patients with suspected tumefactive demyelinating disease.
Schreiner, Simon +13 more
core +1 more source
Objectives: Tumefactive demyelination is a rare form of multiple sclerosis which is characterised by solitary, acute, demyelinating lesions in the central nervous system, usually larger than 2 cm, accompanied by surrounding oedema.
Nayaab Saeed +4 more
doaj +1 more source
Semliki Forest virus induced, immune mediated demyelination: the effect of irradiation [PDF]
Intraperitoneal infection with the avirulent A7(74) strain of the alphavirus Semliki Forest virus (SFV) induces an immune mediated demyelinating encephalomyelitis.
Fazakerley, J K, Webb, H E
core
Tumefactive demyelinating lesions (TDL) represent a diagnostic dilemma for clinicians, and in rare atypical cases a collaboration of a neuroradiologist, a neurologist, and a neuropathologist is warranted for accurate diagnosis.
Maria-Evgenia Brinia (12241238) +5 more
core +1 more source
Multifaceted Biomarkers Suggest a Similar Profile of CNS Pathology in Relapsing and Progressive MS
ABSTRACT Background Relapsing–remitting (RR) and primary progressive (PP) multiple sclerosis (MS) have distinct clinical courses, but underlying pathophysiological differences remain unclear. We compared pathological components between RRMS, PPMS, and other inflammatory and neurodegenerative disorders, leveraging soluble biomarkers and post‐mortem ...
Katelijn M. Blok +12 more
wiley +1 more source
Whether or not recurrent tumefactive demyelinating lesions are a unique form of CNS demyelinating disease or part of the continuum of multiple sclerosis is a question raised by the case report on which this commentary is based.
Weinshenker, B. G.
core +1 more source
Chronic active lesions preferentially localize in watershed territories in multiple sclerosis
Abstract Objective Paramagnetic rim lesions (PRLs) are a biomarker of chronic active lesions (CALs), and an important driver of neurological disability in multiple sclerosis (MS). The reason subtending some acute lesions evolvement into CALs is not known. Here we ask whether a relatively lower oxygen content is linked to CALs.
Ahmad A. Toubasi +14 more
wiley +1 more source
Myelin Oligodendrocyte Glycoprotein Antibody-Associated Encephalitis among the Pediatric Intensive Care Unit Patients: A Comprehensive Clinical Review [PDF]
Background: Myelin oligodendrocyte glycoprotein antibody-associated encephalitis (MOGAE) is an increasingly recognized entity within the MOG antibody-associated disease spectrum in children.
Zienab Mohamed +3 more
doaj +1 more source

