27 results
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D3.316 - Impact of chronic urticaria on the quality of life of patients followed up at a university hospital Nis-Serbia

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D3.305 - Pediatric and Adult Responses to Fourth-Fold Antihistamine Doses: Insights into Efficacy and Safety

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D3.306 - Successful treatment of severe atopic dermatitis in teenage patient with hyper-IgE syndrome (STAT3 mutation)

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D3.307 - Experience with Systemic Emergent Therapies for Moderate-to-Severe Atopic Dermatitis: Insights from an Allergy and Clinical Immunology Department

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D3.308 - Frailty in elderly with C1 Inhibitor Hereditary Angioedema: first evidence from a monocentric ITACA cohort

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D3.309 - Challenges in HAE therapy in children

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D3.310 - Hereditary angioedema (HAE) with factor XIIa mutation successfully treated with icatibant as on-demand therapy and lanadelumab for long-term prophylaxis

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D3.311 - Screening for Hereditary Angioedema in Pediatric Patients with Autoinflammatory Diseases and Chronic Abdominal Pain

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D3.312 - Lymphatic supplementation improves atopic dermatitis in dogs

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D3.313 - Chronic Spontaneous Urticaria and its relationship with Allergies to Aerogenic Fungi: dermographism, skin hyperreactivity, and chemical patterns of inflammation

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D3.314 - Sensitization Profile in Patch Tests with the Portuguese Baseline Series in the Algarve

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D3.315 - Airborne allergic contact dermatitis to dry shampoo

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

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

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

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D1.311 - Treatment Dilemmas in CARMIL2 Deficiency

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

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

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

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