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43 results
D1.274 - Anaphylaxis Risks in Beekeeping: The Importance of Developing a Health Education Program
D1.284 - Trends in Recurrent Anaphylaxis Triggered by Food, Drug, and Insect Allergies from 2015 to 2021: A Population-Based Retrospective Cohort Study Using the National Insurance Claims Database of Japan
D1.275 - Wheat-free diet restore the normal intestinal microbiome structure in patients with wheat-dependent exercise-induced anaphylaxis
D1.276 - Social #anaphylaxis: how social media reveals shifting trends in public health concerns
D1.278 - Chlorhexidine allergy in perioperative anaphylaxis: undeclared and overlooked
D1.279 - Vit v 5: A Chitinase Implicated in Grape-Induced Anaphylaxis
D1.282 - Identification of Thaumatin-like protein (Ole E 13) as a potential allergen in green olives, a case report
D1.283 - Idiopathic anaphylaxis in a child, Alpha-gal syndrome. Is it an entity in children?
D1.285 - Analysis of systemic food reactions in patients sensitized to Bet v1 in Madrid (Spain)
D1.286 - Nebulized inhaled epinephrine versus epinephrine autoinjector for the treatment of food-induced anaphylaxis in young children – a randomized controlled clinical trial
D1.287 - Lipid profiling of Co-factor Induced Anaphylaxis: The Impact of Exercise and Aspirin on metabolism
D1.289 - Severe allergy to albumin after cesarean section
D1.309 - Association of Antenatal Corticosteroids with Risk of Autoimmune Diseases in Children: a Nationwide Cohort Study
D1.308 - Case report: challenges in a long-term prophylaxis in hereditary angioedema (HAE)
D1.310 - Phenotypes of patients with Hereditary Angioedema (HAE): a case series
D1.311 - Treatment Dilemmas in CARMIL2 Deficiency
D1.312 - Acquired C1-inhibitor deficiency angioedema treated with lanadelumab: a case series
D1.313 - Inborn Error of Immunity Associated Inflammatory Bowel Disease at a Tertiary Care Center
D1.315 - Classifying the unclassifiable: diagnosis, characterization, and management of adults with unclassified primary antibody deficiency (unPAD)
D1.316 - Lessons Learned from the Diagnosis and Management of a female pediatric patient with NCF2 Mutations and Chronic Granulomatous Disease
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