Natalia Lorena Fili
A5078546878- Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Urticaria and Related Conditions
- Autoimmune Bullous Skin Diseases
- Blood Coagulation and Thrombosis Mechanisms
- Enzyme function and inhibition
- Vitamin K Research Studies
- Hemophilia Treatment and Research
- Mast cells and histamine
Universidad Católica de Salta
2021
National University of Salta
2017
GA2LEN, the Global Allergy and Asthma European Network, HAE international (HAEi), global umbrella organization for world's hereditary angioedema (HAE) patient groups, have launched their joint ACARE (Angioedema Center of Reference Excellence) program, within GA2LEN's center reference excellence (CORE) initiative. Angioedema is a common, heterogeneous, often debilitating chronic condition frequently challenge physicians affected patients, especially patients suffering from recurrent attacks....
Hereditary angioedema (HAE) is a rare disease. During the last years, many studies and advances have been developed with aim of better understanding pathophysiology, as well optimizing patient management. Several international working groups attempted to clarify standardize care HAE communicated guidelines consensus recommendations. We considered necessary provide recommendations for diagnosis treatment patients in Argentina.A group specialists allergy immunology from Argentina by using...
<title>Abstract</title> PurposeHereditary angioedema (HAE) is a rare genetic disease with hyperactivated contact and kallikrein-kinin systems leading to bradykinin (BK) release edema. SARS-CoV-2 infection results in inflammatory exacerbation. C1 inhibitor (C1-INH) deficiency could aggravate clinical outcomes, HAE patients at greater risk of adverse outcomes COVID-19, however, data are still limited. Our aim was characterize the course severity COVID-19 HAE.MethodsLatin American reference...