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24 results
D2.283 - Beyond the skin. A rare case of contact angioedema due to Methylisothiazolinone
D2.292 - Epinephrine Nasal Powder - a sustainable and reliable option for the treatment of anaphylaxis
D2.293 - Assessment of the Efficacy of Specific Immunotherapy After a Long Break in Asthmatic Patients
D2.278 - National Survey on Perioperative Hypersensitivity Reactions: Evaluating Practices and Challenges in Spanish Hospitals
D2.279 - In an emergency, can YOU really give that adrenaline pen? – the need for structured, further and improved training in Ireland
D2.282 - IgE-mediated anaphylaxis to quinine confirmed with a basophil activation test
D2.284 - Eat the fruit, do not swallow the seed: A rare case of Cucurbitaceae allergy causing anaphylaxis
D2.286 - A case of prawn induced FDEIA
D2.287 - Evaluation of NSAID Hypersensitivity in Children: A Retrospective Analysis
D2.288 - Idursulfase Hypersensitivity Reactions: Unpacking Immunological Mechanisms Beyond Clinical Manifestations
D2.289 - A Cardiovascular Enigma in the Emergency Room
D2.290 - Allergens involved in a case report of anaphylaxis to ginger (Zingiber officinale), a very rare but severe allergy
D2.291 - The level of knowledge of adolescent and young adults about food allergies and anaphylaxis: Key information that can save lives - a pilot study
D3.419 - Prevalence of physical urticaria hives in patients with systemic mastocytosis and their relation to disease course – preliminary data
D3.411 - Targeting MRGPRX2 for the Treatment of Mast Cell-Driven Diseases
D3.412 - MRGPRX2 Specific Activation Signature is Enriched in Atopic Dermatitis Lesions and Wheals from Chronic Spontaneous Urticaria Compared to Adjacent Healthy Skin
D3.413 - Development of the Mastocytosis Symptom Severity Daily Diary (MS2D2) for Non-Advanced Systemic Mastocytosis (NonAdvSM) Patients and Establishing Content Validity
D3.414 - The Phase 2/3 Study of Elenestinib, a Highly Potent and Selective Tyrosine Kinase Inhibitor, in Patients With Indolent Systemic Mastocytosis
D3.415 - Clinical manifestations of Hereditary alpha-tryptasemia (HaT) in Patients with Mast Cell Activation Syndromes
D3.416 - Hereditary Alpha-Tryptasemia: A Case Series
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