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195 results
- D3.130 - Selective IgA Deficiency in the Pediatric Population: A Gateway to Allergies and Autoimmunity
D3.317 - Moderate-to-severe infections and initial SELENA-SLEDAI correlate with the incidence of flares in patients with Systemic Lupus Erythematosus
D3.322 - Acquired chronic granulomatous disease secondary to myelodysplastic disorder
D3.324 - Mastoiditis as complication of Hyper IgM syndrome
D3.326 - A RARE COEXISTENCE: CARD9 DEFICIENCY AND IgG4-RELATED DISEASE IN A PEDIATRIC PATIENT
D3.327 - Use of C1 Inhibitor Subcutaneously in the United Kingdom
D3.328 - Relapsing COVID-19 pneumonia and Helicobacter cineadi cellulitis in a patient with X-linked agammaglobulinemia
D3.332 - Determination of Reference Intervals for IgG, IgA, and IgM Levels by Age in Healthy Adults
D3.348 - A Case of 19p13.3 Microdeletion
D3.349 - Evaluation of natural killer cells in female infertility
D3.138 - Asthma remission in EGPA patients: applicability and concordance of the main international guidelines
D3.193 - Impact of subcutaneous allergen immunotherapy on autoimmune disease development or exacerbations: a cross-sectional study
D3.354 - Selective IgE deficiency in children: its role in autoimmunity
D3.356 - Unconventional T cells in leukocyte adhesion deficiency I (LAD-I)
D3.362 - Use and safety of canakinumab during pregnancy
D3.394 - Anxiety Associated with Parenteral On-Demand Treatment for Hereditary Angioedema Attacks in Patients from Italy
D3.57 - Isoniazid-Induced Lupus in a Filipino Female: A Case Report
D1.308 - Case report: challenges in a long-term prophylaxis in hereditary angioedema (HAE)
D1.310 - Phenotypes of patients with Hereditary Angioedema (HAE): a case series
D1.311 - Treatment Dilemmas in CARMIL2 Deficiency
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