26 results
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D3.306 - Veno-Venous ECMO For Aprotinin-Induced Perioperative Anaphylaxis

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D3.308 - Kounis Syndrome: the allergic myocardial infarction

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D3.313 - Recurrent Anaphylaxis with Elevated Baseline Tryptase Revealing Hereditary Alpha-Tryptasemia with Mast Cell Activation

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D3.314 - Rapid desensitization to intravenous risankizumab after anaphylaxis in a patient with Crohn’s disease: a case report

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D3.315 - Management of Drug Hypersensitivity Reactions in an Oncology Patient: An Atypical Case of Omeprazole Allergy with Pantoprazole Tolerance

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D3.317 - Linguistic Validation of the Turkish Version of the Mastocytosis Control Test (MCT)

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D3.318 - Evaluation of Clinical Predictors and Serum Tryptase Levels in Systemic Mastocytosis

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D3.319 - Clinical Data of Drug Induced Anaphylaxis according to the standardized European Anaphylaxis Registry (NORA)

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D3.320 - Anaphylaxis by Chlorhexidine: A case series

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D3.321 - Cardiac arrest after Iodixanol: a case of non-IgE mediated mast cell activation

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D3.307 - Chlorhexidine-triggered anaphylaxis in a child with multisystem allergy and sickle cell disease: a diagnostic pitfall

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D3.309 - Basophil Activation Test Detects Rocuronium Allergy During the Post-Anaphylactic Refractory Period: A PAMA Case Report

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D3.322 - Successful management with Omalizumab and high-dose venom immunotherapy in a patient with Kounis Syndrome and Clonal Mast Cell Activation Syndrome

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D3.357 - Revealing an Underlying Inborn Error of Immunity in Pediatric Granulomatous Disease: A Case of STAT1 Loss-of-Function–Associated Mendelian Susceptibility to Mycobacterial Disease after BCG Vaccination

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D3.361 - Pulmonary Embolism in a Patient with Hyper IgE (Job) Syndrome Associated with Genetic Thrombophilia: A Rare Case

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D3.362 - Ulcerative Colitis Developing in an Immunodeficiency Patient with CD19 Gene Mutation: A Case Report

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D3.363 - Systemic Lupus Erythematosus in a Patient with Hyper IgM Syndrome

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D3.366 - Experience With Berotralstat In The First Turkish Patients

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D3.367 - Clinical and immunological heterogeneity of 22q11.2 deletion syndrome in children from the Republic of Moldova

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D3.368 - Selective IgE Deficiency in Children: 10-Year Experience