Results 81 to 90 of about 11,219 (248)
Tolosa-Hunt syndrome with general myasthenia gravis involvement
Tolosa-Hunt syndrome is an uncommon disease that exhibits unilateral periorbital pain or headache, accompanied by cranial nerve palsies. Myasthenia gravis is an acquired immune system disease involving the neuromuscular junction. One rare case of Tolosa-Hunt syndrome combined with ocular myasthenia gravis had been reported in the literature, but not ...
Lu, Li, Zhe, Wang, Ming-Ou, Lu
openaire +3 more sources
Myasthenia Gravis Patients with Anti-MuSK Antibodies [PDF]
In myasthenia gravis (MG) patients without detectable anti-acetylcholine receptor (anti-AChR) antibody, referred to as seronegative myasthenia gravis patients, there is a variable proportion of patients with antibodies against the muscle-specific kinase (
Davorka Vranješ +5 more
core +1 more source
An evaluation of nipocalimab for the treatment of generalized myasthenia gravis
Myasthenia gravis (MG) is an autoimmune disease caused by autoantibodies targeting the neuromuscular junction. MG, characterized clinically by fluctuating muscle weakness and fatigability, is traditionally treated primarily with corticosteroids and nonspecific immunosuppressive drugs.
Carlo Antozzi, Marie Fitzgibbon
openaire +2 more sources
Abstract Objective This study aimed to evaluate demographic characteristics, treatment effectiveness, and safety outcomes in patients with migraine undergoing anti‐calcitonin gene‐related peptide (CGRP) treatments regarding the presence of autoimmune diseases. Background CGRP has an important role in migraine pathophysiology through neuronal modulation
María Clara García‐Castillo +37 more
wiley +1 more source
Abstract Objective This study aimed to evaluate whether a single dose of intravenous dexamethasone, when added to standard abortive therapy, reduces relapse of migraine after emergency department (ED) discharge in children and adolescents. Background Migraine is a leading cause of headache presentations to the ED for children and adolescents.
Geneviève Tourigny‐Ruel +3 more
wiley +1 more source
Sneddon's syndrome: clinical and laboratory analysis of 10 cases. [PDF]
Sneddon's syndrome is characterized by livedo reticularis and cerebrovascular lesions. We report the cases of women (mean age, 36.2 +/- 8.1 years) diagnosed with Sneddon's syndrome based on the presence of livedo reticularis and characteristic ...
Akyol, Melih +5 more
core +1 more source
Risk factors for generalization of ocular myasthenia gravis
Purpose: To identify potential risk factors for the generalization of ocular myasthenia gravis (OMG). Design: Retrospective cohort study. Methods: This study was conducted at a tertiary neurology clinic between January 2007 and January ...
Djordjevic, Ivana S +7 more
openaire +3 more sources
CD4+ T Cells Predict Relapse in Pemphigus Vulgaris Treated With Rituximab: A Retrospective Study
ABSTRACT Objective This study evaluated the CD4+ T‐cell role in mediating post‐Rituximab Pemphigus vulgaris (PV) relapse, comparing CD4+ count and CD4+/CD20+ ratio between patients who achieved remission and those who relapsed. Methods The clinical course of 27 PV patients treated with Rituximab was evaluated after a 32‐month median follow‐up. CD4+ and
Simone Liguori +9 more
wiley +1 more source
Exacerbation Rate in Generalized Myasthenia Gravis and Its Predictors
<b><i>Objective:</i></b> The aim of the study was to estimate the exacerbation incidence rate (IR) in acetylcholine receptor antibody (AChR)-positive generalized myasthenia gravis (MG) and its predictors. <b><i>Methods:</i></b> The primary outcome in this retrospective study was to estimate moderate-to ...
Ahmad R, Abuzinadah +4 more
openaire +3 more sources
Abstract This study examines whether underwriting methods—representation, medical examination, extra premiums, and coverage—effectively mitigate adverse selection using data from an insurance company. Regarding representation, we focus on statements disclosing pre‐existing medical conditions.
Chia‐Ling Ho +3 more
wiley +1 more source

