38 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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- D1.336 - Barriers to Normalization with Existing Treatments Among People Living with Hereditary Angioedema in Europe

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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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- D1.338 - Divergent Clinical and Functional Consequences of Canonical NF-κB Pathway Defects

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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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D3.51 - Cardiovascular System Problems in Children Athletes with Allergic Diseases

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D3.53 - Prevalence of allergic sensitization to edible insects in exposed breeders from Thailand

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D3.59 - Occupational Cobalt Contact Dermatitis: Clinical Profile and Work implications

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D3.52 - Clinical spectrum and diagnostic challenges of paediatric angioedema without wheals

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D3.55 - Hereditary angioedema with normal C1-INH: DAB2IP mutation report

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D3.56 - Investigation of Serum Eosinophilic Granule Proteins Levels in Children with Chronic Spontaneous Urticaria

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D3.57 - Respiratory Manifestations Of Ascariasis Mimicking Allergic Disease: A Clinical Case

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D3.58 - Eosinophilic ascites and extreme hypereosinophilia: differential diagnosis through medical treatment

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D3.60 - Allergic reaction in bisoprolol overdose