27 results
Thumbnail

D1.202 - Small-Spotted Catshark Parvalbumin Sensitization in Fish-Allergic Patients

Thumbnail

D1.203 - Pine Nut Allergy in a Pediatric Patient with Multiple Sensitizations to Tree Nuts and Storage Proteins

Thumbnail

D1.204 - Pea-ling Back the Layers: A Systematic Review of Pea Allergies

Thumbnail

D1.205 - Characterization of a cohort of fish allergic portuguese patients

Thumbnail

D1.206 - A 50-year history of IgE-mediated hypersensitivity reactions to Saccharomyces cerevisiae presenting with respiratory symptoms

Thumbnail

D1.207 - “Do nut know what: What is the current role of the prick test and serum IgE in the diagnosis of walnut allergy?

Thumbnail

D1.208 - Clinical relevance of food allergen families

Thumbnail

D1.209 - Pollen and Food Non-Specific Lipid Transfer Proteins: Clinical Presentations and Sensitization Profiles in a Mediterranean Population

Thumbnail

D1.210 - Effects of Omalizumab on Human Basophils in Children with Cow’s Milk Protein Allergy

Thumbnail

D1.212 - IgE mediated allergic reaction to rice

Thumbnail

D1.213 - Exercise-Induced Anaphylaxis in a 18-Year-Old Woman with Egg Allergy and Potential Bird-Egg Syndrome

Thumbnail

D1.214 - Food Allergy:Even in doubt, Challenge Test

Thumbnail

D1.309 - Association of Antenatal Corticosteroids with Risk of Autoimmune Diseases in Children: a Nationwide Cohort Study

Thumbnail

D1.308 - Case report: challenges in a long-term prophylaxis in hereditary angioedema (HAE)

Thumbnail

D1.310 - Phenotypes of patients with Hereditary Angioedema (HAE): a case series

Thumbnail

D1.311 - Treatment Dilemmas in CARMIL2 Deficiency

Thumbnail

D1.312 - Acquired C1-inhibitor deficiency angioedema treated with lanadelumab: a case series

Thumbnail

D1.313 - Inborn Error of Immunity Associated Inflammatory Bowel Disease at a Tertiary Care Center

Thumbnail

D1.315 - Classifying the unclassifiable: diagnosis, characterization, and management of adults with unclassified primary antibody deficiency (unPAD)

Thumbnail

D1.316 - Lessons Learned from the Diagnosis and Management of a female pediatric patient with NCF2 Mutations and Chronic Granulomatous Disease