Results 231 to 240 of about 84,459 (353)

Atypical Pediatric‐Onset Behçet's Disease Presenting With Superior Vena Cava Thrombosis in an Adolescent Male: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Behçet's disease is a chronic, relapsing multisystem vasculitis known for its highly variable clinical spectrum. We report the case of an 18‐year‐old male who presented with progressive headache and facial swelling. Imaging revealed extensive thrombosis involving the dural venous sinuses, superior vena cava, and left brachiocephalic vein ...
Ubaid Ullah   +8 more
wiley   +1 more source

Chikungunya Infection Increases Osteoclastogenic Genes Ex-pression in Blood and Chronic Arthralgia May Be Related to Enhanced Osteoclast Survival

open access: green
Alysson H. Urbanski   +5 more
openalex   +1 more source

Drooling as a Red Flag: Insights From a Case Series in Severe Dermatomyositis With Literature Review

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Dermatomyositis (DM) is a rare idiopathic inflammatory disease characterized by progressive proximal muscle weakness and distinctive dermatologic manifestations. Although dysphagia is a recognized complication of oropharyngeal muscle involvement, drooling (sialorrhea) is infrequently described and may be a marker of severe disease.
Alireza Mirzamohamadi   +9 more
wiley   +1 more source

Dual use of combustible and heated tobacco products associates persistent symptoms with a history of COVID-19: a JASTIS 2023 cross‑sectional study. [PDF]

open access: yesSci Rep
Toyokura E   +12 more
europepmc   +1 more source

Adult‐Onset Still's Disease Complicated by Secondary Hemophagocytic Lymphohistiocytosis: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Adult‐onset Still's disease (AOSD) is a rare autoinflammatory disorder characterized by fever, rash, joint pain, and elevated ferritin levels. Systemic inflammation can trigger an exaggerated immune response, leading to secondary hemophagocytic lymphohistiocytosis (HLH).
Vasileios Patriarcheas   +8 more
wiley   +1 more source

Joint involvement in VEXAS and non-VEXAS clonal haematopoiesis: two clusters from a multicentre regional cohort. [PDF]

open access: yesRMD Open
de Maleprade B   +13 more
europepmc   +1 more source

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