Publications
- EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children2020 | Second Faculty of Medicine
- Novel XIAP mutation causing enhanced spontaneous apoptosis and disturbed NOD2 signalling in a patient with atypical adult-onset Crohn's disease2020 | Second Faculty of Medicine
- Utility of Ruxolitinib in a Child with Chronic Mucocutaneous Candidiasis Caused by a Novel STAT1 Gain-of-Function Mutation2018 | Second Faculty of Medicine, First Faculty of Medicine
- Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia2017 | Second Faculty of Medicine
- Determination of lymphocyte subpopulations (CD3+, CD4+, CD8+, CD19+, CD16,56+) in peripheral blood using flow cytometry [Gate: lymphocytes]Publication without faculty affiliation
- Clinical outcomes, immunogenicity, and safety of BNT162b22 Vaccine in Primary Antibody Deficiency2023 | Second Faculty of Medicine
- TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins2022 | Second Faculty of Medicine, Faculty of Mathematics and Physics, First Faculty of Medicine
- Impact of JAK Inhibitors in Pediatric Patients with STAT1 Gain of Function (GOF) Mutations-10 Children and Review of the Literature2022 | Second Faculty of Medicine, First Faculty of Medicine, Central Library of Charles University
- A novel case of homozygous IFNAR1 deficiency with haemophagocytic lymphohistiocytosis2022 | Second Faculty of Medicine
- Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK2022 | Second Faculty of Medicine
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