Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1111/cea.12869 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Angioedema.
Allergy Asthma Clin Immunol
December 2024
Division of Allergy and Immunology, Department of Medicine, Western University, London, ON, Canada.
Angioedema can occur in the absence of urticaria and can be broadly divided into three main categories: mast cell-mediated (e.g., histamine), non-mast-cell-mediated (bradykinin-induced) and idiopathic angioedema.
View Article and Find Full Text PDFEtiology, Recent Advances, and Clinical Trials Data for the Treatment of Angioedema: A Review.
Rev Recent Clin Trials
October 2024
Department of Pharmaceutics, Lovely Professional University, Phagwara, Punjab, 144001, India.
Angioedema is a health issue that affects parts of the body like the upper pulmonary and gastric pathways and is identified by abrupt, nonpitting enlargement of the skin, mucous membranes, or both. The swelling usually lasts a few hours to 72 hours and may appear as non-puritic, subcutaneous, or submucosal organ edema. It is characterized by localized swelling brought on by the release of histamine.
View Article and Find Full Text PDFClinical features and potential markers of disease in idiopathic non-histaminergic angioedema, a real-life study.
Immunol Res
October 2024
Department of Translational Medical Sciences, University of Naples Federico II, Via Sergio Pansini 5, Naples, 80131, Italy.
Article Synopsis
- Idiopathic non-histaminergic acquired angioedema (InH-AAE) is a rare disease that causes swelling and doesn't respond well to common medications like antihistamines.
- The study looked at 26 patients with InH-AAE to understand their symptoms and possible markers of the disease, collecting a lot of health-related information.
- Findings included changes in specific proteins in the blood and differences in blood vessel shape, helping to improve the understanding of InH-AAE and possibly leading to better treatments in the future.
Contact System Activation and Bradykinin Generation in Patients With Idiopathic Angioedema.
J Investig Allergol Clin Immunol
October 2024
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, SC Medicina - Emostasi e Trombosi, Milan, Italy.
Latent inter-organ mechanism of idiopathic pulmonary fibrosis unveiled by a generative computational approach.
Sci Rep
December 2023
Karydo TherapeutiX, Inc., 2-2-2 Hikaridai, Seika-Cho, Soraku-Gun, Kyoto, 619-0288, Japan.
Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive disease characterized by complex lung pathogenesis affecting approximately three million people worldwide. While the molecular and cellular details of the IPF mechanism is emerging, our current understanding is centered around the lung itself. On the other hand, many human diseases are the products of complex multi-organ interactions.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!