22 results
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D1.13 - A rare case of isolated histaminergic angioedema

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D1.15 - True Mugwort Sensitization Presenting as Severe Atopic Dermatitis: A Diagnostic Challenge

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D1.02 - Sensitization to Sesame Proteins Despite Negative Conventional Testing

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D1.03 - Identification of a Thaumatin-Like Protein as a Shared Allergen in Kiwi and Persimmon: Molecular Analysis in a Case of Anaphylaxis

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D1.08 - Clinical relevance of troponin C (Cra c 6) sensitization in crustacean allergy

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D1.10 - Underrecognition of Anaphylaxis in Children: Gaps in Diagnosis and Management

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D1.11 - Determinants of allergen sensitization and wheal size variability in skin prick testing in a large outpatient cohort

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D1.14 - Biphasic, Refractory, and Persistent Anaphylaxis in Children

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D1.06 - When an alergic reaction turns into a cardiac event: clinical characterization of Kounis Syndrome

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D2.378 - Evaluations of Safety Margins and Response to Deucrictibant Extended-Release (XR) Tablet in Combination with Deucrictibant Immediate-Release (IR) Capsule

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D2.367 - Hepatic Involvement and Inflammatory Bowel Disease in Chronic Granulomatous Disease: A Retrospective Evaluation

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D2.368 - Concurrent Hereditary Angioedema Type I and Common Variable Immunodeficiency Presenting as Suspected Antibiotic Hypersensitivity: Case Report and Literature Review

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D2.370 - Chronic urticaria and autoimmunity: clinical, laboratory and molecular correlations

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D2.374 - Diagnostic delay in children with primary immunodeficiencies: clinical consequences in a single-country cohort from the Republic of Moldova

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D2.375 - Structural lung changes detected by chest CT in pediatric patients with combined immunodeficiencies

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D2.377 - Severe Eosinophilia as an Atypical Initial Presentation of X-Linked Hyper-IgM Syndrome Due to CD40LG Deficiency

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D3.357 - Revealing an Underlying Inborn Error of Immunity in Pediatric Granulomatous Disease: A Case of STAT1 Loss-of-Function–Associated Mendelian Susceptibility to Mycobacterial Disease after BCG Vaccination

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D3.361 - Pulmonary Embolism in a Patient with Hyper IgE (Job) Syndrome Associated with Genetic Thrombophilia: A Rare Case

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D3.362 - Ulcerative Colitis Developing in an Immunodeficiency Patient with CD19 Gene Mutation: A Case Report

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D3.363 - Systemic Lupus Erythematosus in a Patient with Hyper IgM Syndrome