Publications
- A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literature2016 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Augmenting Clinical Interpretability of Thiopurine Methyltransferase Laboratory Evaluation2014 | Second Faculty of Medicine
- Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopenia2013 | Second Faculty of Medicine
- Immunosuppressive therapy combining anti-thymocyte globulin and cyclosporine A in childhood acquired aplastic anaemia - long term-outcomes and risks2012 | Second Faculty of Medicine
- Hemophagocytic lymphohistiocytosis as a manifestation of visceral leishmaniasis2002 | Second Faculty of Medicine
- Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome2024 | Second Faculty of Medicine
- Severe Acute Kidney Injury in Children as a Rare Complication of Paroxysmal Cold Hemoglobinuria2023 | Second Faculty of Medicine, Central Library of Charles University
- Schimke immunoosseous dysplasia: an ultra-rare disease. a 20-year case series from the tertiary hospital in the Czech Republic2023 | Second Faculty of Medicine
- TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins2022 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Mathematics and Physics
- Hydrops fetalis and failure of hematopoietic stem cell transplantation - A long route to the diagnosis of SPTA1-associated hereditary spherocytosis2022 | Second Faculty of Medicine, Central Library of Charles University
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