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30 results
D2.100 - The usefulness of the forced oscillation technique in the diagnosis of bronchial asthma in seniors
D2.111 - Wheeze phenotypes in infants whose mothers have asthma
D2.99 - A mechanosensitive cytoskeleton protein talin2 involved in asthma pathogenesis
D2.102 - Adult Gut Microbiota and Metabolomics in Different Phenotypes of Asthma
D2.103 - Exploring association between lung function, asthma and epigenetic predisposition to obesity
D2.104 - Dissecting the molecular mechanisms underlying TSLP-driven non-type 2 inflammatory responses in severe asthma
D2.105 - Clinical remission of severe asthma: 5-year follow-up
D2.106 - Molecular Clustering Using microRNA Expression Profiles in Pediatric Asthma Reveals Differential Corticosteroid Responsiveness
D2.107 - Effect of n-3 long-chain polyunsaturated fatty acid and vitamin D supplementation on human lung organoids
D2.108 - Real-life experience after 6 months with Tezepelumab in specialized asthma units across northern Spain
D2.109 - Interleukin-17A gene polymorphism contribute to the elderly asthma susceptibility: evidences from a case-control study
D2.110 - MicroRNA Signatures of Pediatric Obesity-Associated Asthma: Identifying Molecular Links Between Obesity and Asthma in Children
D2.112 - The Impact of Obesity in Asthma and Small Airway Dysfunction: Prevalence, Clinical characteristics, and Predictors
D2.114 - Insights from the BREATHE Study: Comorbidity Burden and Biomarker Trends in Severe Asthma Patients
- D1.323 - Clinical Experience with Lanadelumab for Hereditary Angioedema in Kazakhstan
D3.317 - Moderate-to-severe infections and initial SELENA-SLEDAI correlate with the incidence of flares in patients with Systemic Lupus Erythematosus
D3.322 - Acquired chronic granulomatous disease secondary to myelodysplastic disorder
D3.324 - Mastoiditis as complication of Hyper IgM syndrome
D3.326 - A RARE COEXISTENCE: CARD9 DEFICIENCY AND IgG4-RELATED DISEASE IN A PEDIATRIC PATIENT
D3.327 - Use of C1 Inhibitor Subcutaneously in the United Kingdom
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