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Poster topics
  • Aerobiology and pollution (41)
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  • Thematic Poster Session (262)
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Session Reference
  • L-TPS01 (11)
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312 results
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D3.349 - Evaluation of natural killer cells in female infertility

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D3.138 - Asthma remission in EGPA patients: applicability and concordance of the main international guidelines

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D3.193 - Impact of subcutaneous allergen immunotherapy on autoimmune disease development or exacerbations: a cross-sectional study

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D3.306 - Successful treatment of severe atopic dermatitis in teenage patient with hyper-IgE syndrome (STAT3 mutation)

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D3.310 - Hereditary angioedema (HAE) with factor XIIa mutation successfully treated with icatibant as on-demand therapy and lanadelumab for long-term prophylaxis

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D3.354 - Selective IgE deficiency in children: its role in autoimmunity

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D3.356 - Unconventional T cells in leukocyte adhesion deficiency I (LAD-I)

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D3.362 - Use and safety of canakinumab during pregnancy

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D3.382 - Evaluation of Serum Arginase-1 Levels in Chronic Urticaria

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D3.394 - Anxiety Associated with Parenteral On-Demand Treatment for Hereditary Angioedema Attacks in Patients from Italy

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D1.292 - Assessing Quality of Life in Chronic Spontaneous Urticaria: Insights from DLQI Scores

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D1.295 - Clinical, Laboratory and Prognostic Evaluation of Antinuclear Antibody Positive and Negative Children with Chronic Urticaria

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D1.298 - Topical gluconolactone induces immune tolerance in cutaneous lupus erythematosus in human and mice

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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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