29 results
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D1.103 - Two cases of discrepancy between fractional exhaled nitric oxide and airway eosinophils in asthma

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D1.104 - Severe Bronchial Asthma Phenotypes in a Referral Tertiary Center in Saudi Arabia

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D1.105 - Lichen Planus induced by treatment of severe eosinophilic asthma with biological therapy

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D1.106 - Grape polyphenols reduce the concentration of LPS in patients with asthma

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D1.107 - Polyphenol concentrate reduces CRP in asthma patients who have had COVID-19

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D1.108 - Grape polyphenols increase the concentration of BPI in asthma patients who have had SARS-CoV-2

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D1.109 - Predominance of eosinophilic pathogenetic mechanisms in a severe allergic asthma patient on biologic therapy

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D1.110 - Analysis of clinical and anamnestic risk factors of bronchial asthma in children

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D1.111 - Improving severe asthma through psychological management of traumatic life events

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D1.112 - Managing patients with Type 2 inflammation in a joint interdisciplinary “United Airways Clinic” at Lund University Hospital, Sweden

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D1.113 - Severe Asthma and Depression: the Overlooked Burden

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D1.114 - The Hidden Costs of Severe Asthma Treatment: Unveiling the Iatrogenic Burden

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D1.115 - Post-emergency asthma management

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D3.419 - Prevalence of physical urticaria hives in patients with systemic mastocytosis and their relation to disease course – preliminary data

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D3.411 - Targeting MRGPRX2 for the Treatment of Mast Cell-Driven Diseases

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D3.412 - MRGPRX2 Specific Activation Signature is Enriched in Atopic Dermatitis Lesions and Wheals from Chronic Spontaneous Urticaria Compared to Adjacent Healthy Skin

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D3.413 - Development of the Mastocytosis Symptom Severity Daily Diary (MS2D2) for Non-Advanced Systemic Mastocytosis (NonAdvSM) Patients and Establishing Content Validity

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D3.414 - The Phase 2/3 Study of Elenestinib, a Highly Potent and Selective Tyrosine Kinase Inhibitor, in Patients With Indolent Systemic Mastocytosis

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D3.415 - Clinical manifestations of Hereditary alpha-tryptasemia (HaT) in Patients with Mast Cell Activation Syndromes

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D3.416 - Hereditary Alpha-Tryptasemia: A Case Series