15 results
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D1.308 - Case report: challenges in a long-term prophylaxis in hereditary angioedema (HAE)

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D1.310 - Phenotypes of patients with Hereditary Angioedema (HAE): a case series

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D1.311 - Treatment Dilemmas in CARMIL2 Deficiency

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D1.312 - Acquired C1-inhibitor deficiency angioedema treated with lanadelumab: a case series

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D1.313 - Inborn Error of Immunity Associated Inflammatory Bowel Disease at a Tertiary Care Center

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D1.315 - Classifying the unclassifiable: diagnosis, characterization, and management of adults with unclassified primary antibody deficiency (unPAD)

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D1.316 - Lessons Learned from the Diagnosis and Management of a female pediatric patient with NCF2 Mutations and Chronic Granulomatous Disease

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D1.317 - A Retrospective Analysis of Dengue-Associated Hemophagocytic Lymphohistiocytosis in a Dengue-Endemic Country

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D1.318 - Extending Lanadelumab Dosing Intervals to Every 4 Weeks With Sustained Effectiveness for Hereditary Angioedema Attack Prevention: An Analysis From the Final ENABLE Study Data

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D1.319 - The Silent Threat of Hereditary Angioedema in Children: Single Center Experience

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D1.322 - A Prescription for Lower Immunity: The Hidden Cost of Certain Psychiatric Medications

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D1.323 - Concurrence of essential mixed cryoglobulinemia and cold agglutinin disease: a matter of shared light chains. Case series and literature review

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D1.324 - Evaluation of the Potential for Sebetralstat to Cause Pseudo-allergic Reactions

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D1.325 - Autoantibodies to interferon-gamma: clinical features, treatment outcomes, and in-vitro monitoring of disease

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D2.57 - Recurrent pleural effusion in patient with hereditary angioedema: a case report