16 results
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D2.383 - Ocular Cicatricial Pemphigoid: Experience with Methotrexate immunosuppression in a case series from Mar del Plata, Argentina

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D2.381 - Early Infantile Immune Dysregulation with an Atopic Phenotype: A Case of Genetically Confirmed Otulipenia

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D2.382 - Contribution of Clinical and Laboratory Findings to Genetic Testing Decisions and Diagnostic Yield in Patients with Suspected Primary Immunodeficiency

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D2.384 - Early inflammatory manifestations in a child carrying a heterozygous TREX1 variant: possible evolving interferonopathy?

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D2.386 - Intravenous Immunoglobulin–Associated Severe Prolonged Neutropenia: A Rare but Life-Threatening Complication in Primary Immunodeficiency

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D2.391 - Assessment of Small Airway Dysfunction by Impulse Oscillometry in Patients with CVID and Selective IgA Deficiency

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D3.243 - Food allergy in children with inherited epidermolysis bullosa: possible role of transcutaneous sensitization and features of the clinical course

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D3.240 - Differential microRNA expression in chronic spontaneous urticaria in relation to treatment response

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D3.241 - How Clinical Control of Chronic Urticaria influence in mental health

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D3.242 - SDRIFE induced by multiple systemic corticosteroids

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D3.244 - STK4 Deficiency Presenting with Epidermodysplasia Verruciformis

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D3.246 - A Novel Mutation in a Case of Deficiency of Interleukin-1 Receptor Antagonist in a Filipino Male Child

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D3.247 - Skin Involvement Is One Of The Common Signs In Children With Inborn Errors Of Immunity

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D3.251 - Prevention of Irritant Contact Dermatitis Among Dental Students

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D3.252 - Water-induced localized urticaria: A rare case of aquagenic urticaria

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D3.253 - Two Infant Cases Diagnosed with Bullous Mastocytosis, a Rare Variant of Diffuse Cutaneous Mastocytosis