Publikace
- EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children2020 | 2. lékařská fakulta
- Novel XIAP mutation causing enhanced spontaneous apoptosis and disturbed NOD2 signalling in a patient with atypical adult-onset Crohn's disease2020 | 2. lékařská fakulta
- Utility of Ruxolitinib in a Child with Chronic Mucocutaneous Candidiasis Caused by a Novel STAT1 Gain-of-Function Mutation2018 | 2. lékařská fakulta, 1. lékařská fakulta
- Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia2017 | 2. lékařská fakulta
- Stanovení lymfocytárních subpopulací CD3+ , CD4+ , CD8+ , CD19+ , CD16,56+ v periferní krvi průtokovou cytometrií [Gate: lymfocytární]Publikace bez příslušnosti k fakultě
- Clinical outcomes, immunogenicity, and safety of BNT162b22 Vaccine in Primary Antibody Deficiency2023 | 2. lékařská fakulta
- TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins2022 | 2. lékařská fakulta, Matematicko-fyzikální fakulta, 1. lékařská fakulta
- Impact of JAK Inhibitors in Pediatric Patients with STAT1 Gain of Function (GOF) Mutations-10 Children and Review of the Literature2022 | 2. lékařská fakulta, 1. lékařská fakulta, Ústřední knihovna
- A novel case of homozygous IFNAR1 deficiency with haemophagocytic lymphohistiocytosis2022 | 2. lékařská fakulta
- Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK2022 | 2. lékařská fakulta
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