Results 131 to 140 of about 161,435 (256)
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
Glymphatic System Dysfunction and its Associated Factors in Wilson's Disease: A DTI–ALPS Study
Glymphatic function, assessed by DTI‐ALPS index, was impaired in neurological Wilson's disease compared with hepatic phenotype and controls. Age, AST, and UWDRS‐I score independently predicted dysfunction, linking neurodegeneration, liver injury, and altered glymphatic activity. ABSTRACT Background Wilson's disease (WD) is a genetic disorder of copper (
Ling Zhu +14 more
wiley +1 more source
Histopathologic Analysis of the Morpho‐Functional Zones of the Human Acetabular Labrum
ABSTRACT The structural and functional adaptation of soft tissues to mechanical load controls their ability to withstand injury and influences their capacity for healing. Similar to the knee meniscus, the acetabular labrum exhibits zonal differences in mechanical load distribution, resulting in distinct regions with unique structural and functional ...
Abdulaziz A. Alomiery +4 more
wiley +1 more source
Fibrous dysplasia is a benign disease of the bone characterized by the replacement of normal bone with fibro-osseous tissue.
Nickisa Hodgson; Jessica Chang; Adelita Vizcaino; Charles Eberhart; Andrew Carey; Amanda Henderson; Timothy McCulley
core
Proteomic Signatures of Noise‐Induced Hearing Loss in the Mouse Cochlea
ABSTRACT Hearing loss affects over 1.5 billion people worldwide and has substantial social, educational, and economic consequences. Although genetic studies have identified numerous hearing‐loss‐associated genes, the molecular changes accompanying noise‐induced hearing loss (NIHL) remain incompletely understood.
Ana Carla Batissoco +6 more
wiley +1 more source
ABSTRACT Dermatomyositis (DM) is a rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and distinctive cutaneous manifestations. It is frequently associated with underlying malignancies, making recognition of paraneoplastic features crucial.
Manisha Chapagain +4 more
wiley +1 more source
ABSTRACT Hypopharyngeal cysts are a rare cause of pediatric upper airway obstruction and may present acutely, even in previously asymptomatic children. Early endoscopic evaluation is essential in children with stridor and unexplained airway compromise, as prompt surgical excision can be both diagnostic and curative.
Fathalla Noori +5 more
wiley +1 more source
Fibrous Dysplasia of Bone [PDF]
Brenda L, Nelson, Lester D R, Thompson
openaire +2 more sources
ABSTRACT Background Crohn's disease (CD) is a multifactorial inflammatory bowel disease (IBD) characterized by impaired epithelial barrier integrity, excessive immune hyperactivation, and gut microbiota perturbations. Cumulative evidence supports the role of the intestinal epithelial barrier, immune system and gut microbiota in the progression of CD ...
Qing Lai +3 more
wiley +1 more source
ABSTRACT Hypoplastic myelodysplastic syndrome (MDS) often overlaps clinically with aplastic anemia and frequently involves clonal hematopoiesis. Thrombopoietin receptor agonists (TPO‐RAs), including eltrombopag, are increasingly used to treat cytopenias in hypoplastic marrow failure syndromes; however, their long‐term effects on clonal dynamics and ...
Kyoko Yoshihara +7 more
wiley +1 more source

