34 results
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D2.314 - Late Presentation of Cutaneous Chronic Graft Versus Host Disease – A Case Report

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D2.309 - Descriptive Study of Chronic Urticaria Under Treatment with Omalizumab: Our Experience

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D2.310 - Dysregulation of barrier function and distribution of nerve cells in a mouse model of atopic dermatitis

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D2.311 - Real World Web Survey on the Burden of Urticaria

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D2.312 - Impact of metabolic disorders on immune dysregulation in psoriasis and atopic dermatitis

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D2.313 - Importance of non-itchy erythema marginatum as a prodromal symptom of hereditary angioedema attacks

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D2.315 - Clinical features and Progress of Diagnosis and Therapy of Hereditary Angioedema in China: A Systemic Review of Published Cases

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D2.316 - The role of Tumor necrosis factor ligand superfamily member 15 in Atopic dermatitis

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D2.317 - The role of sirtuin 2 (SIRT2) in atopic dermatitis

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D2.318 - Triggers and prodromal indicators of angioedema attacks in hereditary angioedema patients

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D2.319 - Advancing Diagnosis and Management of Hereditary Angioedema in Brazil: Insights from the first 704 patients of a Multicenter Registry

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D2.322 - Quality of life of families with children suffering from chronic urticaria

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D2.323 - Higher neonatal urinary phthalate are associated with the development of infantile atopic dermatitis

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D2.324 - Psychological Burden Associated with Injectable HAE On-Demand Treatments: A Patient and Caregiver Interview Study

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D3.333 - Unveiling the Role of PGD2/CRTH2 Signaling in Antigen-Specific IgE Production

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D3.334 - Characterization of novel nickel specific cd4+ regulatory T cells from a nickel sensitized joint implant failure patient

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D3.335 - The role of activated leukocyte cell-adhesion molecule in hyperoxia induced acute lung injury

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D3.336 - CC variant of the -634G/C polymorphism of the VEGF gene is associated with higher HDL levels in patients with type 1 diabetes mellitus

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D3.337 - The -634G/C polymorphism of the VEGF gene affects BPI concentration in patients with type 1 diabetes mellitus

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D3.338 - The sCD14 level in patients with type 1 diabetes mellitus may be related to the -786T/C polymorphism of the NOS3 gene