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30 results
D1.309 - Association of Antenatal Corticosteroids with Risk of Autoimmune Diseases in Children: a Nationwide Cohort Study
D1.308 - Case report: challenges in a long-term prophylaxis in hereditary angioedema (HAE)
D1.310 - Phenotypes of patients with Hereditary Angioedema (HAE): a case series
D1.311 - Treatment Dilemmas in CARMIL2 Deficiency
D1.312 - Acquired C1-inhibitor deficiency angioedema treated with lanadelumab: a case series
D1.313 - Inborn Error of Immunity Associated Inflammatory Bowel Disease at a Tertiary Care Center
D1.315 - Classifying the unclassifiable: diagnosis, characterization, and management of adults with unclassified primary antibody deficiency (unPAD)
D1.316 - Lessons Learned from the Diagnosis and Management of a female pediatric patient with NCF2 Mutations and Chronic Granulomatous Disease
D1.317 - A Retrospective Analysis of Dengue-Associated Hemophagocytic Lymphohistiocytosis in a Dengue-Endemic Country
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
D1.319 - The Silent Threat of Hereditary Angioedema in Children: Single Center Experience
D1.322 - A Prescription for Lower Immunity: The Hidden Cost of Certain Psychiatric Medications
D1.323 - Concurrence of essential mixed cryoglobulinemia and cold agglutinin disease: a matter of shared light chains. Case series and literature review
D1.324 - Evaluation of the Potential for Sebetralstat to Cause Pseudo-allergic Reactions
D1.325 - Autoantibodies to interferon-gamma: clinical features, treatment outcomes, and in-vitro monitoring of disease
D2.342 - Changes of MMP-9 and MMP-12 in response of acute viral infection in virtual model of macrophages
D2.343 - Use of IDDA 2.1 score in Common Variable Immunodeficiency (CVID): a single center experience
D2.344 - Unraveling the Mysteries of Chronic Granulomatous Disease: A Case of detected Protein Deficiency Amidst Negative Genetic Screening
D2.345 - Conformations of HVEM engaged in its Trans and Cis interactions are caused by two kinds of post-translational folding
D2.346 - Assessment of the safety of allogenic natural killer cells in the treatment of metastatic colon cancer
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