Results 41 to 50 of about 3,236 (115)
Abstract Objective This study aims to assess the prevalence of head and neck (ENT) symptoms in patients with sarcoidosis. Study Design 1:4 matched‐case control study. Setting Patients with and without sarcoidosis who enrolled in the All of Us Research Program and consented to electronic medical record use.
Peter J. Attia +6 more
wiley +1 more source
Imperatorin Mitigates Rosacea‐Like Inflammation by Modulating the Crosstalk Between JNK1 and STAT1
IMP treatment disrupts the interaction between JNK1 and STAT1, thereby attenuating STAT1 activity. This interference subsequently diminishes the phosphorylation and nuclear translocation of STAT1, which ultimately results in a reduced production of inflammatory cytokines and chemokines.
Xiaoxue Wang, Zexin Zhu
wiley +1 more source
Our experience with granulomatous rhinitis. A new occupational disease.
From the study of two groups of patients-133 cases of Extrinsic Pulmonary Granulomatoses (E.P.G.) and 360 cases of exposure to various occupational environments who were routinely submitted to nasal biopsies the authors conclude that granulomatous rhinitis is either a manifestation of E.P.G.
R, Avila +4 more
openaire +1 more source
ABSTRACT Background Acupoint embedding (AEM) therapy merges traditional acupuncture with modern biomaterials to treat various diseases and for cosmetic uses, especially obesity and facial anti‐aging. Research Objective To examine complications from acupuncture embedding therapy (AEM), focusing on foreign body granulomas and infections.
Xiazhen Xu +4 more
wiley +1 more source
Churg Strauss Syndrome after Polypectomy in Asthmatic and Allergic Patients
Churg Strauss Syndrome (CSS) is a form of primary vasculitis that is characterized by severe eosinophilia and often granulomatous inflammation as well as history of asthma or allergy.
Fallah Tafti Saeid +2 more
doaj
Bullous Vasculitis in Eosinophilic Granulomatosis with Polyangiitis: A Case Report
Introduction: Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis affecting small- and medium-sized vessels. It is characterized by multiorgan involvement and can lead to severe outcomes if not diagnosed promptly.
Tiraporn Phumwiriya, Charussri Leeyaphan
doaj +1 more source
Schistosomiasis remains the most devastating neglected tropical disease, affecting over 240 million people world-wide. The disease is caused by the eggs laid by mature female worms that are trapped in host’s tissues, resulting in chronic Th2 driven ...
Paballo Mosala +15 more
doaj +1 more source
Wegener’s granulomatosis in ophthalmic practice. Clinical case
Wegener’s granulomatosis (WG) or granulomatosis with polyangiitis is a primary systemic necrotizing vasculitis of small and medium-sized vessels with the development of foci of granulomatous inflammation.
M. M. Bikbov +2 more
doaj +1 more source
Widespread Skin Lesions in an Italian Man
JEADV Clinical Practice, Volume 5, Issue 1, Page 333-336, March 2026.
Rebecca Donadoni +7 more
wiley +1 more source
A Case of Wegener's Granulomatosis
Background: Wegener is a granulomatous necrotizing vasculitis characterized by a predilection to affect the upper and lower respiratory tracts and, in most cases, the kidneys.
Mansoor Karimifar +5 more
doaj

