13 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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D3.260 - 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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D3.258 - Not just a rash: a delayed diagnosis of allopurinol-induced dress syndrome