Type II hereditary angioedema with an apparently de novo SERPING1 mutation in China: A case report and family screening. [PDF]
Guan Z +5 more
europepmc +1 more source
Performance of PEN‐FAST and CEPH‐FAST for Cephalosporin Allergy Delabeling
Evaluation of PEN‐FAST and CEPH‐FAST in 100 patients with cephalosporin allergy labels showed that PEN‐FAST reliably identified low‐risk patients suitable for direct drug challenge, while CEPH‐FAST demonstrated reduced diagnostic performance. ABSTRACT Background Unverified antibiotic allergy labels lead to suboptimal antimicrobial prescribing and ...
Deniz Göcebe +4 more
wiley +1 more source
Vascular endothelial growth factor (VEGF) emerging as a mediator of hereditary angioedema (HAE). [PDF]
Giavina-Bianchi P, Aun MV, Kalil J.
europepmc +1 more source
Exploring Floristic Diversity and Medicinal Plant Uses in Venda, Limpopo, South Africa
ABSTRACT Plants have been an important source of medicine for thousands of years. To better understand the current diversity and usage of medicinal plants, floristic studies are essential. This report documents an expedition conducted in the Venda region of Limpopo, South Africa. The study was carried out in Shanzha and surrounding villages, as well as
Gurusamy Manikandan +2 more
wiley +1 more source
Abstract Neurodegenerative Langerhans cell histiocytosis (ND‐LCH) is a severe and debilitating complication of LCH with no effective treatment. In this study, we assessed the efficacy of MAPK inhibitors (MAPKi) in a large cohort of children with ND‐LCH. We included pediatric patients with ND‐LCH who received MAPKi between 2013 and 2025.
Francesco Pegoraro +38 more
wiley +1 more source
Pain management in patients with hereditary angioedema: A case report. [PDF]
Li X, Ran Y, Zuo C, He S, Ma Y, Li X.
europepmc +1 more source
Recurrent angioedema manifestation and treatment response in two patients from different families caring the myoferlin gene mutation: case series. [PDF]
Fomina DS +12 more
europepmc +1 more source
MEAT PIES: Mammalian Meat Allergy in Patients Investigated for Gastrointestinal Symptoms
ABSTRACT Background Alpha‐gal syndrome (AGS), an IgE‐mediated allergy to galactose‐α‐1,3‐galactose acquired via tick bites, often presents with a delayed gastrointestinal (GI) phenotype without anaphylaxis. We evaluated a local diagnostic guideline in a Far North Queensland gastroenterology outpatient clinic.
Elias Bitzer +2 more
wiley +1 more source
Real-world quality of life in patients with hereditary angioedema receiving lanadelumab or other long-term prophylaxis. [PDF]
Davis-Lorton M +8 more
europepmc +1 more source
Trends in Asthma‐Rhinitis Allergic Multimorbidity and Polysensitization in China: The CARRAD Study
This cross‐sectional study highlights the increasing prevalence of allergic diseases and comorbidities under environmental conditions of rapid modernization in China. Our observations underline the relevance of the allergic comorbidities phenotype at the clinical and public health levels.
Wanjun Wang +41 more
wiley +1 more source

