29 results
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D2.342 - Changes of MMP-9 and MMP-12 in response of acute viral infection in virtual model of macrophages

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D2.343 - Use of IDDA 2.1 score in Common Variable Immunodeficiency (CVID): a single center experience

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D2.344 - Unraveling the Mysteries of Chronic Granulomatous Disease: A Case of detected Protein Deficiency Amidst Negative Genetic Screening

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D2.345 - Conformations of HVEM engaged in its Trans and Cis interactions are caused by two kinds of post-translational folding

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D2.346 - Assessment of the safety of allogenic natural killer cells in the treatment of metastatic colon cancer

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D2.347 - Allergen-Specific T Cells to House Dust Mite are absent on the circulation of local allergic rhinitis patients

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D2.348 - Clinical Course of Hereditary Angioedema Patients Transitioning off Androgens

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D2.349 - Hereditary Angioedema in Bulgaria: an update on patient characteristics and treatment modalities

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D2.350 - CVID: the crossroad between immune dysregulation, autoimmunity and cancer

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D3.260 - Bempedoic acid allergy in a patient with hypercholesterolemia

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- D3.262 - Bempedoic acid allergy in a statin-intolerant patient with hypercholesterolemia

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D3.252 - Azithromycin and Mycoplasma pneumonia: an unusual Stevens-Johnson syndrome case

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D3.256 - Is an Early-Type Hypersensitivity Reaction Possible with Both Peroral and Parenteral Anticoagulant Drugs? A Successful 2-Day Peroral Desensitization Protocol to Rivaroxaban

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D3.257 - Two cases of propofol anaphylaxis revealed by provocation test

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D3.258 - Probable drug- induced Enterocolitis Syndrome (DIES) caused by Amoxicillin

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D3.259 - KOLLIPHOR : An excipient to be futher explored

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D3.263 - Rare case of anaphylaxis to lidocaine in skin testing during perioperative anaphylaxis investigation

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D3.264 - Pioneering study evaluating the Basophil Activation Test (BAT), PENFAST and skin sensitization to penicillin in patients with gestational syphilis

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D3.290 - Manifestations of allergic skin lesions in the early childhood and adult population: Epidemiological manifestations of diseases

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D3.291 - Hereditary angioedema with normal C1Inh and PLG mutation treated with tranexamic acid : Beware of the risk of thrombosis