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Poster topics
  • AllergoOncology (1)
  • Allergy diagnosis (15)
  • Drug allergy (15)
  • Epidemiology (2)
  • x Immune deficiencies and autoimmunity (13)
  • Pediatrics (1)
  • Systems medicine (1)
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Poster categories
  • Thematic Poster Session (13)
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Session Reference
  • L-TPS06 (8)
  • L-TPS07 (2)
  • L-TPS11 (3)
  • L-TPS18 (1)
  • L-TPS20 (2)
  • L-TPS21 (4)
  • TPS11 (1)
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  • TPS16 (14)
  • TPS17 (1)
  • TPS28 (1)
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  • x TPS40 (12)
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  • x TPS54 (1)
  • TPS56 (2)
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  • TPS65 (8)
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13 results
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D2.325 - Long-Term Safety and Efficacy of Oral Deucrictibant for Treatment of Hereditary Angioedema Attacks: Results of the RAPIDe-2 Extension Study

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D2.326 - Long-Term Safety and Efficacy of Oral Deucrictibant for Prophylaxis in Hereditary Angioedema: Data Snapshot Results of the CHAPTER-1 Open-Label Extension Study

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D2.327 - Outcome of hematopoietic stem cells transplantation for inborn error of immunity in Vietnam

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D2.328 - Comparison of the frequency of viral infections in immunocompromised patients receiving immunoglobulin by different routes

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D2.329 - Impact of Berotralstat on Quality of Life among Patients with Hereditary Angioedema: Pooled Analysis of the APeX-2 and APeX-J Trials

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D2.330 - Hereditary angioedema prophylaxis therapy: berotralstat and lanadelumab safety profile

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D2.331 - Lanadelumab safety and efficacy in patients aged ≥12 with hereditary angioedema (HAE) in China for long-term prophylaxis (LTP): An open-label, multicenter study

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D2.334 - Real-World Effectiveness of Lanadelumab in Hereditary Angioedema: A 12-Month Retrospective Study at a Single Center in Colombia

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D2.336 - Evolution of Hereditary Angioedema Prophylaxis in Hungary Over Four Decades (1979-2023)

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D2.338 - The Effect of Covid-19 Vaccines on Adult Primary Immunodeficiency Patients

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D2.339 - Hereditary Angioedema Burden: Impact on Quality of Life, Disease Management, and Sleep Health

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D2.340 - A high prevalence of autoimmune diseases and autoantibodies in patients with hereditary angioedema in Sweden

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D3.57 - Isoniazid-Induced Lupus in a Filipino Female: A Case Report

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