23 results
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D1.90 - Remission of asthma on biological therapy: one center experience

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D1.98 - MV130 drives the differentiation of human monocytes into dendritic cells with antiallergic properties

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D1.102 - Md

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D1.88 - Mepolizumab and intestinal parasitic infection: A case report

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D1.91 - Baseline characteristics and main clinical outcomes of patients receiving tezepelumab in the framework of use in Special Situations prior to commercialization in Spain (T-ROSS Study)

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D1.92 - Results from the EGPAware Delphi study on Red Flags for Suspicion of Eosinophilic Granulomatosis with Polyangiitis (EGPA): current management in Europe

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D1.93 - ICS use trajectories in severe asthma patients on benralizumab: real-life data from 3-years follow-up

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D1.94 - Impact of overweight and obesity on clinical remission and Response to Biologics in Severe Asthma Patients

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D1.95 - Dupilumab-induced eosinophilia: a transient effect

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D1.96 - Impact of Dupilumab-induced Eosinophilia on Pulmonary Function Tests and Patient Reported Outcomes Measures (PROMs)

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D1.99 - Exploring the relationship between 6 minutes walk test (6MWT) performance and lung function in Severe Asthma and CRSwNP

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D1.435 - Eosinophilic diseases: from nasal polyposis, eosinophilic asthma to EGPA (Eosinophilic Vasculitis with PolyAngioitis), evaluation of possible biomarkers of disease evolution

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D1.437 - Frequency of SNPs associated with pharmacogenetic phenotypes in Asthma in two Colombian populations

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D1.439 - Is allergic conjunctivitis tip of the allergic iceberg ?

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D1.440 - Single cell pipeline to improve immune cell annotation through comparison of multiple bioinformatic methods

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- D1.323 - Clinical Experience with Lanadelumab for Hereditary Angioedema in Kazakhstan

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D3.317 - Moderate-to-severe infections and initial SELENA-SLEDAI correlate with the incidence of flares in patients with Systemic Lupus Erythematosus

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D3.322 - Acquired chronic granulomatous disease secondary to myelodysplastic disorder

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D3.324 - Mastoiditis as complication of Hyper IgM syndrome

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D3.326 - A RARE COEXISTENCE: CARD9 DEFICIENCY AND IgG4-RELATED DISEASE IN A PEDIATRIC PATIENT