Results 1 to 10 of about 616 (213)

Hospitalizations due to Angioedema without Urticaria in a Portuguese Center: Five Year Retrospective Study

Acta Médica Portuguesa, 2019
Introduction: Hospitalizations due to angioedema are important especially in debilitating or life-threatening situations. The aim of this study was to evaluate the frequency and etiology of angioedema without urticaria in hospital admissions.
Joana Cosme, Amélia Spínola, Manuel Branco Ferreira, Manuel Pereira Barbosa   +3 more
doaj   +1 more source

Anesthesia in a patient with hereditary angioedema [PDF]

, 2022
Hereditary angioedema (HAE) is a rare genetic disease caused by an autosomal dominant mutation that results in an alteration of the gene encoding the activated C1 esterase inhibitor protein (C1-INH), causing deficiency or dysfunction of C1-INH.
Carlos Enríquez Fernández Montoya, Dayné García García, Zhachel Alejandro Redondo Gómez   +2 more
core   +1 more source

Hereditary Angioedema [PDF]

New England Journal of Medicine, 2020
Anna, Valerieva, Maria, Staevska, Jonathan A, Bernstein   +2 more
  +10 more sources

Pseudoangioedema [PDF]

, 2017
Angioedema is a rapid, localized and temporary subcutaneous edema, which targets the lips, eyelids, gastrointestinal and respiratory mucosa resulting in abdominal pain, asthma and even serious life‐threatening conditions like airway obstruction.
Akarsu, Sevgi, Canturk, Ecem
core   +2 more sources

Analyses of Spontaneous Adverse Drug Reaction Databases Using Descriptive and Inferential Statistics [PDF]

, 2020
The presented cumulative dissertation summarizes four scientific research papers of analyses assessing data of the adverse drug reaction (ADR) database of the Federal Institute for Drugs and Medical Devices (BfArM) and the European ADR database ...
Dubrall, Diana
core  

ANGIOEDEMA HEREDITÁRIO: UMA ATUALIZAÇÃO. [PDF]

, 2015
Objective: Hereditary angioedema is a genetic disease with autosomal dominance inheritance characterized by quantitative and qualitative deficiency of C1 inhibitor, resulting in edema of multiples organs.
Chong Neto, Herberto José, Machado, Ana Flávia, Riedi, Carlos Antônio, Rosário, Nelson Augusto, Thomaz, José Eduardo   +4 more
core   +2 more sources

Pediatric hereditary angioedema [PDF]

Pediatric Allergy and Immunology, 2013
Abstract Hereditary angioedema ( HAE ) is a lifelong illness characterized by recurrent swelling of the skin, intestinal tract, and, ominously, the upper airway. It is caused by inadequate activity of the protein C1‐inhibitor, with dysfunction in the kallikrein/bradykinin ...
openaire   +3 more sources

[Hereditary angioedema].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1989
Hereditary angioedema is a rare disease, transmitted as an autosomal dominant trait. The disease usually manifests as acute subcutaneous or submucosal swellings and abdominal pain of two to five days duration. When localized to head or throat, life-threatening edema of the larynx may occur. The disease is caused by reduced amount of active C1 inhibitor.
A, Sabbah, I, Marsollier, V, Trouillard
  +6 more sources

Anesthetic Management of Labor in a Woman with Hereditary Angioedema

Acta Médica Portuguesa
N/a.
Inês P. Rodrigues, Maria M. Armindo, Luísa Marinho   +2 more
doaj   +1 more source

Novel SERPING1 Genetic Variant in Two Family Members with Hereditary Angioedema

Acta Médica Portuguesa
Hereditary angioedema is a rare, autosomal dominant, genetic disorder characterized by recurrent episodes of angioedema. Over 800 SERPING1 gene variants have been reported, and their clinical profiles and causal genetic variants are highly heterogeneous.
Sofia Cosme Ferreira, Alexandra Rosa, Filipa Sousa, Alejandro Mendoza-Alvarez, Rafaela González-Montelongo, Ariel Callero, Carlos Flores, Rita Câmara   +7 more
doaj   +1 more source