19 results
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D3.260 - Shiitake-Induced Flagellate Dermatitis: Case Series from Kazakhstan

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D3.261 - Orphan Diseases In Allergology - Melkersson-Rosenthal Syndrome

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D3.264 - Delayed Type Hypersensitivity Injection Site Reaction Induced By Liraglutide

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D3.265 - Gleish syndrome: A case report

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D3.266 - Component-Resolved Delayed Hypersensitivity to Piperacillin/Tazobactam and Clavulanic Acid Despite Structural Divergence

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D3.267 - Statistics of Contributing Factors to Atopic Dermatitis in Children

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D3.256 - A Child with Mastocytosis presenting with generalized severe Pruritus: A Diagnostic Pitfall

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D3.258 - Not just a rash: a delayed diagnosis of allopurinol-induced dress syndrome

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- D1.340 - Attack burden and patient-reported outcomes in adults with hereditary angioedema: associations with quality of life, pain, and coping strategies

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- D1.336 - Barriers to Normalization with Existing Treatments Among People Living with Hereditary Angioedema in Europe

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- D1.337 - Long-Term Safety, Tolerability, and Effectiveness of Berotralstat in Hereditary Angioedema: Interim Analysis of the APeX-N Post-Authorization Study

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- D1.338 - Divergent Clinical and Functional Consequences of Canonical NF-κB Pathway Defects

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- D1.339 - Renal and urinary tract disorders in inborn errors of immunity

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- D1.341 - Severe Atopic Features with Prematurity and Ichthyosis: Ichthyosis Prematurity Syndrome

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- D1.342 - Case Report: Off-Label Dosage of Berotralstat in Hereditary Angioedema

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- D1.343 - Common Variable Immunodeficiency Associated Enteropathy: A Single-Center Experience

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- D1.344 - Hidden Immunodeficiency in Adult Bronchiectasis: Lymphocyte Subsets, Humoral Defects, and Genetic Findings

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- D1.346 - Clinically significant gastrointestinal endoscopic findings in asymptomatic patients with common variable immunodeficiency

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- D1.347 - Lanadelumab in Children with Hereditary Angioedema Aged 2 to