33 results
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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

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D2.480 - Features of the molecular sensitization profile in children with autism spectrum disorder

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D2.485 - Comprehensive Understanding of the Characteristics of Pediatric Pollen Allergy Patients

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D2.486 - Levels of house dust mite in dust settlements are associated with risk for allergic rhinitis in children

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D2.489 - B-Cell Subset Reconstitution After Rituximab-Containing Chemotherapy in Children and Adolescents With Non-Hodgkin Lymphoma: A Single-Center Experience

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D2.478 - HEREDITORY ANGIOEDEMA - A case report

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D2.477 - Nationwide Survey of Healthcare Transition from Paediatric to Adult Services for Allergic Diseases in Japan

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D2.479 - The bullous pemphigoid in a baby

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D2.481 - Severe obstructive syndrome in children with bronchopulmonary malformations

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D2.482 - Neuroendocrine Cell Hyperplasia of Infancy (NEHI): Report of 7 Cases