29 results
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D1.327 - Genetic Analysis of Children with Suspected Immunodeficiency: Mimickers of Inborn Errors of Immunity

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D1.329 - Late-Childhood Diagnosis of DNA Methyltransferase 3B Deficiency-ICF1 Syndrome

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D1.322 - Clinical Cardiovascular Safety Assessment of Oral Deucrictibant

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D1.323 - Assessing Immune Responses to Conjugate Pneumococcal Vaccination in Infants with Transient and Unclassified Hypogammaglobulinemia:Insights from a Tertiary Pediatric Center

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D1.324 - JAK Inhibitors in the Treatment of Chronic Mucocutaneous Candidiasis in a Patient with STAT1 Gain-of-Function Mutation

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D1.326 - Behind The Scenes: Primary Immunodeficiencies in Pediatric Eosinophilic Gastrointestinal Diseases

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D1.328 - CARD11 Dominant-Negative Mutation Presenting with Early Severe Bacterial Sepsis, Viral Susceptibility, and Alopecia Totalis in a Child

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D1.330 - Two different clinical presentations, two same immunological features in Purin nucleoside phosporilase deficiency

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D1.331 - Analysis of early complement parameters and C1INH values in newborns with a positive family history of HAE-C1INH

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D1.333 - Digital clinical registry pilot for hereditary angioedema: standardized monthly real-world monitoring of C1 inhibitor deficiency in Serbia

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D1.334 - Association of Multiple Endocrinopaties with Immune Dysregulation, Allergies and Primary Immunodeficiency

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D2.480 - Features of the molecular sensitization profile in children with autism spectrum disorder

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D2.485 - Comprehensive Understanding of the Characteristics of Pediatric Pollen Allergy Patients

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D2.486 - Levels of house dust mite in dust settlements are associated with risk for allergic rhinitis in children

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D2.489 - B-Cell Subset Reconstitution After Rituximab-Containing Chemotherapy in Children and Adolescents With Non-Hodgkin Lymphoma: A Single-Center Experience

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D2.478 - HEREDITORY ANGIOEDEMA - A case report

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D2.477 - Nationwide Survey of Healthcare Transition from Paediatric to Adult Services for Allergic Diseases in Japan

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D2.479 - The bullous pemphigoid in a baby

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D2.481 - Severe obstructive syndrome in children with bronchopulmonary malformations

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D2.482 - Neuroendocrine Cell Hyperplasia of Infancy (NEHI): Report of 7 Cases