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Lung|March 31, 2018
The Variants in the 3' Untranslated Region of the Matrix Metalloproteinase 9 Gene as Modulators of Treatment Outcome in Children with AsthmaSandra Dragicevic, Mitja Kosnik, Aleksandra Divac Rankov, et al.
Current Microbiology|June 28, 2006
High prevalence of multidrug resistance and random distribution of mobile genetic elements among uropathogenic Escherichia coli (UPEC) of the four major phylogenetic groupsMatija Rijavec, Marjanca Starcic Erjavec, Jerneja Ambrozic Avgustin, et al.
Acta Clinica Croatica|August 1, 2019
HEREDITARY ANGIOEDEMA DUE TO C1-INHIBITOR DEFICIENCY IN PEDIATRIC PATIENTS IN CROATIA - FIRST NATIONAL STUDY, DIAGNOSTIC AND PROPHYLACTIC CHALLENGESLjerka Karadža-Lapić, Marko Barešić, Renata Vrsalović, et al.
Biomolecules|January 8, 2025
Cellular and Humoral Response After Induction of Protection and After Finishing Hymenoptera Venom ImmunotherapyAjda Demšar Luzar, Matija Rijavec, Mitja Košnik, et al.
International Archives of Allergy and Immunology|June 23, 2012
House dust mite-specific immunotherapy alters the basal expression of T regulatory and FcεRI pathway genesBranko Pevec, Mira Radulovic Pevec, Asja Stipic Markovic, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 16, 2025
Hereditary α-tryptasemia is Associated With Anaphylaxis to Antibiotics and Monoclonal AntibodiesPeter Korošec, Jonathan J Lyons, Manca Svetina, et al.
Biomedicines|March 28, 2024
Prospective Observational Study of COVID-19 Vaccination in Patients with Thoracic Malignancies: Adverse Events, Breakthrough Infections and Survival OutcomesUrska Janzic, Andrej Janzic, Abed Agbarya, et al.
Vaccines|June 28, 2023
A Three-Dose mRNA COVID-19 Vaccine Regime Produces Both Suitable Immunogenicity and Satisfactory Efficacy in Patients with Solid CancersUrska Janzic, Urska Bidovec-Stojkovic, Peter Korosec, et al.
Frontiers in Immunology|March 10, 2025
Cold-induced anaphylaxis: new insights into clinical and genetic characteristicsMojca Bizjak, Peter Korošec, Mitja Košnik, et al.
Gene|April 28, 2024
The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiencyNina Rupar, Julij Šelb, Mitja Košnik, et al.
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