Abstract Background and Objectives Global demand for immunoglobulin (Ig) continues to rise, driven by expanding clinical indications and limited plasma supply. In England, use increased annually despite earlier demand‐management efforts, with substantial regional variation and prescribing for indications lacking evidence of benefit.
Claire Bethune +5 more
wiley +1 more source
Necrobiotic Xanthogranuloma (NXG): Dermoscopic and Reflectance Confocal Microscopic Findings and Review of Treatment with Intravenous Immunoglobulin (IVIG). [PDF]
Pawlus Z +4 more
europepmc +1 more source
Potential alternatives in treatment of kawasaki disease to reduce the extremely rare risk of reye syndrome. [PDF]
Johnson EJ +4 more
europepmc +1 more source
What Matters Most: A Case of Pemphigus Vulgaris in a Nonagenarian Physician
Journal of the American Geriatrics Society, EarlyView.
Svetlana Bagdasarov +6 more
wiley +1 more source
ABSTRACT Thymoma‐associated myasthenia gravis (TAMG) is frequently refractory, particularly when complicated by myasthenic crisis in advanced invasive disease. Complement C5 inhibitors and neonatal Fc receptor (FcRn) inhibitors have expanded the treatment of acetylcholine receptor (AChR) antibody‐positive generalized myasthenia gravis; however, their ...
Yuta Kizuka +9 more
wiley +1 more source
The hidden threat: understanding anti-PF4 disorders without proximate heparin exposure. [PDF]
Liu Z, Li Y, Ma L, Wang X, Cui Y.
europepmc +1 more source
POEMS Syndrome: 2026 Update on Diagnosis, Risk‐Stratification, and Management
ABSTRACT Disease Overview POEMS syndrome is a life‐threatening syndrome due to an underlying plasma cell neoplasm. The major criteria for the syndrome are polyneuropathy, clonal plasma cell disorder (PCD), sclerotic bone lesions, elevated vascular endothelial growth factor, and the presence of Castleman disease.
Angela Dispenzieri
wiley +1 more source
Fetal and Neonatal Alloimmune Thrombocytopenia in the Middle East: A Confirmed Case Highlighting Immunogenetic Diversity and Evidence-Based Neonatal Management. [PDF]
Haj Mohamad H +6 more
europepmc +1 more source
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu +23 more
wiley +1 more source
The Autophagy-Inflammasome Axis as a Molecular Switch: From Persistent Inflammation to Vascular Remodeling in IVIG-Resistant Kawasaki Disease. [PDF]
Zhang R, Zhang J, Yang Y, Wang Y, Cao H.
europepmc +1 more source

