Publikace
- 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
- Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK2022 | 2. lékařská fakulta
- A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia2020 | 2. lékařská fakulta, 1. lékařská fakulta, Přírodovědecká fakulta, Ústřední knihovna
- EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children2020 | 2. lékařská fakulta
- CVID-Associated Tumors: Czech Nationwide Study Focused on Epidemiology, Immunology, and Genetic Background in a Cohort of Patients With CVID2019 | 2. lékařská fakulta, 1. lékařská fakulta, Lékařská fakulta v Hradci Králové
- Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects2018 | 2. lékařská fakulta
- Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia2017 | 2. lékařská fakulta
- High-resolution Antibody Array Analysis of Childhood Acute Leukemia Cells2016 | 2. lékařská fakulta
- Clinical outcomes, immunogenicity, and safety of BNT162b22 Vaccine in Primary Antibody Deficiency2023 | 2. 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
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