23 results
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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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D3.290 - Manifestations of allergic skin lesions in the early childhood and adult population: Epidemiological manifestations of diseases

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D3.291 - Hereditary angioedema with normal C1Inh and PLG mutation treated with tranexamic acid : Beware of the risk of thrombosis

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D3.292 - "Evaluating Inflammatory Markers in Chronic Spontaneous Urticaria: Impact of Omalizumab Treatment"

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D3.293 - Acrodermatitis chronica atrophicans in the field of scleroderma

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D3.295 - Mental health support for atopic dermatitis patients in the Republic of Kazakhstan

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D3.296 - Urticaria activity, quality of life and disease control in chronic spontaneous urticaria patients in Kazakhstan

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D3.298 - Monomorphic maculo-papular late age onset cutaneous mastocytosis

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D3.299 - Cholinergic urticaria treated with dupilumab

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D3.302 - Elevated Kocuria rhizophila contributing to repair of skin barrier function in patients with atopic dermatitis

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D3.303 - Contact Dermatitis and Rhinoconjunctivitis due to Palisander Wood Exposure in a Cabinetmaker

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D3.304 - Monitoring skin inflammation in atopic dermatitis by non-invasive sampling through skin tape stripping for multiplex protein analysis is complementary to serum biomarkers

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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