Results 91 to 100 of about 616 (213)
Qualidade de vida de pacientes com angioedema hereditário em Santa Catarina: avaliação através do questionário AE-Qol [PDF]
, 2019 TCC(graduação) - Universidade Federal de Santa Catarina. Centro de Ciências da Saúde. Medicina.Introdução: angioedema hereditário (AEH) é um distúrbio autossômico dominante que se manifesta como crises de angioedema imprevisíveis, incapacitantes e ...
Bertoli, Andrezza Fabrízia
core
Anaphylactic transfusion reaction to group B platelets related to alpha‐gal syndrome: A case report
Transfusion, EarlyView.Abstract Background Alpha‐gal syndrome (AGS), a distinct form of IgE‐mediated hypersensitivity to the carbohydrate galactose‐α‐1,3‐galactose (α‐Gal), typically occurs after repeated tick bites and leads to allergic reactions after ingestion of mammalian meat.
Oscar Andre Hinojosa +2 more
wiley +1 more source
GUIDELINES FOR THE DIAGNOSIS AND TREATMENT OF HEREDITARY ANGIOEDEMA [PDF]
, 2014 Hereditarni angioedem (HAE) rijetka je, ali potencijalno za život opasna bolest zbog nepredvidivih napadaja bezbolnih, ograničenih, recidivirajućih otoka supkutanog ili submukoznog, intersticijskog tkiva u trajanju od nekoliko sati do nekoliko dana ...
Asja Stipić Marković +11 more
core +1 more source
Google searches show persistent use of outdated terminology for angioedema in Germany
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Sophia Neisinger +3 more
wiley +1 more source
Chronic Lower Lip Swelling due to Granulomatous Cheilitis
Clinical Case Reports, Volume 14, Issue 5, May 2026.ABSTRACT Granulomatous cheilitis should be considered in the differential diagnosis of persistent, unexplained orofacial swelling, particularly when standard treatments fail.
Jesus Ruiz, Jacob Garner
wiley +1 more source
Hereditary angioedema revisited [PDF]
Allergy and Asthma Proceedings, 2018 Joseph A, Bellanti, Russell A, Settipane
openaire +2 more sources
Edema angioneurotico en el embarazo [PDF]
, 2019 En este trabajo de titulación se presenta el estudio de edema angioneurótico en el embarazo, con la presentación de un caso clínico del HOSPITAL PROVINCIAL GENERAL DOCENTE DE RIOBAMBA, en una paciente primigesta de 22 años de edad, con antecedentes de ...
Carrillo Bravo, Edison Antonio
core
Biphasic, Refractory, and Persistent Anaphylaxis in Children
Clinical and Translational Allergy, Volume 16, Issue 5, May 2026.ABSTRACT Background A Delphi consensus report refined anaphylaxis phenotypes as biphasic, refractory, and persistent anaphylaxis (BA, RA, and PA). To date, no study in either pediatric or adult populations has comprehensively evaluated the full spectrum of anaphylaxis phenotypes as outlined in this consensus.
Gizem Koken +8 more
wiley +1 more source
Journal of General and Family Medicine, Volume 27, Issue 3, May 2026.ABSTRACT Acquired angioedema (AAE) due to C1 inhibitor deficiency can present as acute abdomen. A 24‐year‐old woman developed severe abdominal pain and bowel wall edema initially suggestive of hereditary angioedema, but genetic testing excluded it. She later manifested fever, arthritis, rash, and serological abnormalities consistent with systemic lupus
Seiji Shiota +2 more
wiley +1 more source
2025 Consensus Clinical Management Guidelines for Niemann‐Pick Disease Type C
Journal of Inherited Metabolic Disease, Volume 49, Issue 3, May 2026.ABSTRACT In 2018, the International Niemann‐Pick Disease Alliance (INPDA) and the International Niemann‐Pick Disease Registry (INPDR) developed and published comprehensive clinical management guidelines to support inclusive and standardized care pathways in Niemann‐Pick disease type C (NPC)—an ultra‐rare, autosomal recessive, neurovisceral lysosomal ...
Tarekegn Hiwot +33 more
wiley +1 more source