Publikace
- 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
- Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK2022 | 2. lékařská fakulta
- Natural Course of Activated Phosphoinositide 3-Kinase Delta Syndrome in Childhood and Adolescence2021 | 2. lékařská 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
- EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children2020 | 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
- Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised?2017 | 2. lékařská fakulta
- Imunofenotypizace a jiné využití průtokové cytometrie u akutních leukémií2015 | 2. lékařská fakulta
- Aberrantly expressed CEACAM6 is involved in the signaling leading to apoptosis of acute lymphoblastic leukemia cells2010 | 2. lékařská fakulta
- Clinical outcomes, immunogenicity, and safety of BNT162b22 Vaccine in Primary Antibody Deficiency2023 | 2. lékařská fakulta
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