21 results
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D1.349 - Early Diagnosis of WHIM Syndrome in Infancy: A Case with a De Novo CXCR4 Mutation

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D1.348 - Retrospective Evaluation of Laboratory and Clinical Characteristics of Pediatric Patients Diagnosed with IgG Subclass Deficiency and Receiving Intravenous Immunoglobulin Replacement Therapy

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D1.350 - Selective IgA deficiency and its association with allergic and autoimmune diseases

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D1.351 - Chronic urticaria and autoimmunity: clinical, laboratory and molecular associations

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D1.353 - A Rare Cause of Recurrent Infections: SIFD Syndrome

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D1.354 - Possible Association of a MYOF Loss-of-Function Variant With Recurrent Angioedema: Overlap Between Chronic Spontaneous Urticaria and Normal-C1 Hereditary Angioedema? A Case Report

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D1.355 - Familial Recurrent Angioedema with Normal C1-Inhibitor: A Clinical Case Series Suggestive of HAE with Normal C1-INH

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D1.356 - Atypical association of anti-EJ and anti-RNA polymerase III antibodies in a patient referred for interstitial lung disease

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D1.357 - Atypical case of common variable immune deficiency with granulomatous lymphocytic interstitial lung disease

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D1.363 - Long-Acting Prophylactic Injection BW-20805: Remarkable and Sustained HAE Attack Reduction — Updated Analysis from an Ongoing Phase 2 Study

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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