33 results
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D1.414 - The Clinical Course in a normal C1-Inhibitor Hereditary Angioedema family with Factor XII mutation

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D1.416 - Regulatory T Cells Induced by B cells Decreased Osteoclast Activity and Alleviated Disease Severity of Collagen Antibody Induced Arthritis

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D1.418 - An EBP Gene Variant in a Child with Immunodeficiency: A Case from the Chondrodysplasia Pontata Spectrum

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D1.419 - The management of Immunological Diseases in Internal Medicine Departments

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D1.420 - Lymphoma in CVID: on the edge between immune dysregulation and malignancy

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D1.404 - Live Renal Transplantation Outcome in Egyptian Cohort: A Single Center Study

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D1.405 - Establishment of a Mouse Nasal Epithelial Cell Air–Liquid Interface Culture System and Its Application in Mucosal Barrier Research

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D1.407 - Real-world patient characterization, prior long-term prophylactic prescribing patterns, and treatment outcomes for adults on berotralstat with hereditary angioedema in Japan

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D1.409 - Regulation of the intestinal epithelial barrier by the endocannabinoid system

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D1.413 - A Novel Variant of CORO1A Gene Contributing to The Development of Primary Immunodeficiency in Children

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D1.415 - Regulatory T‑Cell Deficiency and NF‑κB/IL‑1β Activation in Dilated Cardiomyopathy

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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