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
- 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
- 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
- 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
- Minimal Residual Disease-Guided Intermittent Dosing in Patients With Cancer: Successful Treatment of Chemoresistant Anaplastic Large Cell Lymphoma Using Intermittent Lorlatinib Dosing2022 | 2. lékařská fakulta
- Partial RAG deficiency in humans induces dysregulated peripheral lymphocyte development and humoral tolerance defect with accumulation of T-bet(+) B cells2022 | 2. lékařská fakulta
- Somatic Mutations in Oncogenes Are in Chronic Myeloid Leukemia Acquired De Novo via Deregulated Base-Excision Repair and Alternative Non-Homologous End Joining2021 | 2. lékařská fakulta, Fakulta tělesné výchovy a sportu, 1. lékařská fakulta
- Natural Course of Activated Phosphoinositide 3-Kinase Delta Syndrome in Childhood and Adolescence2021 | 2. lékařská fakulta, 1. lékařská fakulta
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