20 results
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D3.166 - Attention-deficit/hyperactivity disorder (ADHD) in asthmatic children

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D3.168 - Clinical Department of Allergy Center in Linköping

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D3.169 - Paediatric Severe Acute Respiratory Infections in Malta: A Three-Year Review

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D3.171 - Validation of the Kazakh Version of the Asthma Quality of Life Questionnaire (AQLQ) for Clinical Use in Adult Patients with Asthma

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D3.173 - Switching from Dupilumab to Tezepelumab in a Child with Severe Asthma and Atopic Dermatitis: Clinical Considerations and Therapeutic Implications

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D3.174 - Short-term tolerance of omlyclo, the omalizumab biosimilar

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D3.175 - Algorithm for Biologics Selection in Severe Asthma

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D3.178 - Assessment of blood rheological properties in children with bronchial asthma

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D3.179 - Longitudinal breath profiling of exhaled volatile organic compounds differentiates viral-induced asthma exacerbation from clinical control

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D2.373 - Characterizing the clinical allergic profile of Romanian adult patients with inborn errors of immunity: results from a tertiary center

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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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D2.369 - Acute Myeloid Leukemia in a Patient With X-linked Agammaglobulinemia

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

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D2.371 - Hematologic Findings in Primary Immunodeficiency Disorders: A Single-Center Experience

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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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D2.376 - Mevalonate kinase deficiency: An analysis of a Slovakian Cohort of MKD patients

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