Publications
- Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK2022 | Second Faculty of Medicine
- Comprehensive Molecular Profiling for Relapsed/Refractory Pediatric Burkitt Lymphomas-Retrospective Analysis of Three Real-Life Clinical Cases-Addressing Issues on Randomization and Customization at the Bedside2020 | Second Faculty of Medicine
- CVID-Associated Tumors: Czech Nationwide Study Focused on Epidemiology, Immunology, and Genetic Background in a Cohort of Patients With CVID2019 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- 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
- Laboratory testing for the presence of minimal residual disease using DNA-based RQ-PCR for clonal rearrangements of Ig/TCR defined by PCR or massive parallel sequencing (NGS)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
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