100 results
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001399 - Can Mepolizumab at asthma doses prevent the development of vasculitis in patients with EGPA?

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001410 - A Rare Case: Anaphylaxis Induced by Melon Seed

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001414 - Recognition of a Heat-Resistant Beef Allergen: Molecular Analysis in a Patient with Multiple Meat and Fish Allergy

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001426 - Clinical and Genetic Characterization of Hereditary Alpha-Tryptasemia: A Case Series

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001458 - Multisensitization to Chicken, Turkey, Rooster and Whey Proteins: Molecular Allergen Characterization by IgE–Western Blot

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001490 - Comparison of skin prick tests with allergen extracts and molecular allergy diagnostics for allergen-specific immunotherapy decision-making in pollen allergy

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001498 - Clinical heterogeneity of Eosinophilic Esophagitis in children

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001542 - Immediate Hypersensitivity to Systemic Corticosteroids: Two Case Reports with Safe Alternative Identification

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001614 - Biological Sensitization Patterns in Suspected Egg Allergy in Tunisia : A Real-Life Laboratory-Based Study

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001679 - Alpha-gal sensitization as a cause of allergy to heparins and collagen

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001757 - Suspected Beta-Lactam Allergy in Young Children: A Delabeling Approach

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001828 - DRESS syndrome or Bullous pemphigoid? A losartan-induced severe exanthema beyond limits

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001856 - Eosinophilic esophagitis (EoE). A case report

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001867 - Excipients under suspicion: A diagnosis challenge in adverse reactions to drugs and vaccines. A case report

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001899 - Efficacy of Omalizumab in Isolated Angioedema as An Uncommon Phenotype of Chronic Spontaneous Urticaria (one-centre experience)

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001971 - Omalizumab‑Assisted Accelerated Oral Immunotherapy In Alpha‑Gal Syndrome: A Case Report

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002001 - Comparative analysis of psoriasis and cancer frequency in patients and their families

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002007 - Quercus pollen as the primary sensitizer in patients with PR-10 sensitization in Salamanca

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002038 - Exercise-Associated Anaphylaxis Complicated by Type II Kounis Syndrome in a Patient With Chronic Coronary Artery Disease

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002112 - Heterozygous IL6ST Mutation–Associated Rare Primary Immunodeficiency: A Case Report