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Poster topics
Poster available until
  • Monday 29 June 2026 (5)
  • Until platform closure (5)
Poster categories
  • Thematic Poster Session (10)
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Session Reference
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21 results
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D1.172 - Parallel Trajectories of Lung Function and Allergic Sensitization in Childhood Asthma: A 7-Year Prospective Study

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D1.180 - Hidden fragility behind optimal ACT score: identifying silent-risk phenotypes through clinical-biological dissociation

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D1.182 - Relationship between eHealth Literacy and Medication Adherence in Patients with Asthma: The Mediating Role of Self-Efficacy

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D1.171 - Real-World Exacerbation Outcomes After AIR Therapy Rescue Implementation: Toward a SABA-Free Era

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D1.173 - Sputum Tryptase Identifies Airway Mast Cell Activation Across Asthma Phenotypes

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D1.174 - Framing ADAM17 alterations across bronchial, sputum and nasal sites in asthma and controls

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D1.175 - Clinical Phenotypes of Difficult-to-treat and Mild Asthma Defined by Cluster Analysis

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D1.176 - Prognostic Evaluation of the Allergic March in Patients with Atopic Dermatitis

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D1.177 - Turkish Validity and Reliability of the Medication Adherence Report Scale for Asthma (MARS-A) in Adolescents with Asthma

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D1.178 - Real-World Comparison of Inhaled Corticosteroid Monotherapy versus Fixed-Dose Inhaled Corticosteroid–Long-Acting Beta-2 Agonist Combinations in Children Aged 6–11 Years with Persistent Asthma

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- D1.340 - Attack burden and patient-reported outcomes in adults with hereditary angioedema: associations with quality of life, pain, and coping strategies

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- D1.336 - Barriers to Normalization with Existing Treatments Among People Living with Hereditary Angioedema in Europe

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- D1.337 - Long-Term Safety, Tolerability, and Effectiveness of Berotralstat in Hereditary Angioedema: Interim Analysis of the APeX-N Post-Authorization Study

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- D1.338 - Divergent Clinical and Functional Consequences of Canonical NF-κB Pathway Defects

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- D1.339 - Renal and urinary tract disorders in inborn errors of immunity

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- D1.341 - Severe Atopic Features with Prematurity and Ichthyosis: Ichthyosis Prematurity Syndrome

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- D1.342 - Case Report: Off-Label Dosage of Berotralstat in Hereditary Angioedema

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- D1.343 - Common Variable Immunodeficiency Associated Enteropathy: A Single-Center Experience

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- D1.344 - Hidden Immunodeficiency in Adult Bronchiectasis: Lymphocyte Subsets, Humoral Defects, and Genetic Findings

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- D1.346 - Clinically significant gastrointestinal endoscopic findings in asymptomatic patients with common variable immunodeficiency

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