26 results
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- D1.340 - Attack burden and patient-reported outcomes in adults with hereditary angioedema: associations with quality of life, pain, and coping strategies

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- D1.337 - Long-Term Safety, Tolerability, and Effectiveness of Berotralstat in Hereditary Angioedema: Interim Analysis of the APeX-N Post-Authorization Study

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- D1.339 - Renal and urinary tract disorders in inborn errors of immunity

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- D1.341 - Severe Atopic Features with Prematurity and Ichthyosis: Ichthyosis Prematurity Syndrome

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- D1.342 - Case Report: Off-Label Dosage of Berotralstat in Hereditary Angioedema

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- D1.343 - Common Variable Immunodeficiency Associated Enteropathy: A Single-Center Experience

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- D1.344 - Hidden Immunodeficiency in Adult Bronchiectasis: Lymphocyte Subsets, Humoral Defects, and Genetic Findings

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- D1.346 - Clinically significant gastrointestinal endoscopic findings in asymptomatic patients with common variable immunodeficiency

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- D1.347 - Lanadelumab in Children with Hereditary Angioedema Aged 2 to

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D2.326 - The frequency of hereditary α-tryptasemia (HαT) in patenits with insect venom anaphylaxis and in patients with mastocytosis – preliminary results

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D2.324 - Anaphylaxis in very early childhood: An ongoing challenge

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D2.325 - Desensitization of Olipudase alfa-induced anaphylaxis in a child with chronic neurovisceral acid sphingomyelinase deficiency and ochoa syndrome

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D2.327 - Patient and caregiver perspectives on sublingual adrenaline for anaphylaxis: findings from an international survey

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D2.329 - Profilin-mediated anaphylaxis with cofactor

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D2.331 - An Adult Case of Cofactor-Induced Anaphylaxis Associated with Physical Exercise

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D2.350 - Exploring the Psychological Burden of Hereditary Angioedema Using the Pictorial Representation of Illness and Self Measure (PRISM): Updated Insights from a Prospective Real-Life Cohort

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D2.351 - Germline Variant in the GNAI2 Gene Associated with Severe Immune Dysregulation and Autoimmune Hemolytic Anemia in a Pediatric Patient

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D2.352 - Epidermodysplasia verruciformis as a sign for STK4 deficiency

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D2.353 - Same Disease, Different Clinical Phenotypes: A20 Haploinsufficiency

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D2.354 - Evaluation of Subjective Sleep Quality and Psychological Status in Adult Patients with Inborn Errors of Immunity