109 results
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D2.343 - Use of IDDA 2.1 score in Common Variable Immunodeficiency (CVID): a single center experience

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D2.344 - Unraveling the Mysteries of Chronic Granulomatous Disease: A Case of detected Protein Deficiency Amidst Negative Genetic Screening

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D2.349 - Hereditary Angioedema in Bulgaria: an update on patient characteristics and treatment modalities

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D2.350 - CVID: the crossroad between immune dysregulation, autoimmunity and cancer

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D2.54 - Basophil Activation Test for Chronic Spontaneous Urticaria: the experience of a paediatric allergy centre

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D2.57 - Recurrent pleural effusion in patient with hereditary angioedema: a case report

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- D3.124 - Severe asthma associated with hereditary angioedema type 1 and other pathologies

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- D3.130 - Selective IgA Deficiency in the Pediatric Population: A Gateway to Allergies and Autoimmunity

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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

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D3.327 - Use of C1 Inhibitor Subcutaneously in the United Kingdom

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D3.328 - Relapsing COVID-19 pneumonia and Helicobacter cineadi cellulitis in a patient with X-linked agammaglobulinemia

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D3.332 - Determination of Reference Intervals for IgG, IgA, and IgM Levels by Age in Healthy Adults

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D3.348 - A Case of 19p13.3 Microdeletion

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D3.349 - Evaluation of natural killer cells in female infertility

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D3.138 - Asthma remission in EGPA patients: applicability and concordance of the main international guidelines

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D3.193 - Impact of subcutaneous allergen immunotherapy on autoimmune disease development or exacerbations: a cross-sectional study

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D3.306 - Successful treatment of severe atopic dermatitis in teenage patient with hyper-IgE syndrome (STAT3 mutation)