Publications
- Deficit of GATA-2 transcription factor: new immunodeficiency syndrome with broad phenotype. First patients diagnosed in the Czech Republic and review of the literature2013 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Pilsen
- Leukemia surfaceome analysis reveals new disease-associated features2013 | Second Faculty of Medicine
- Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)2012 | Second Faculty of Medicine
- Hemophagocytic lymphohistiocytosis syndrome2010 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- B-cell reconstitution after allogeneic SCT impairs minimal residual disease monitoring in children with ALL2008 | Second Faculty of Medicine
- Unrelated partially matched lymphocyte infusions in a patient with complete DiGeorge/CHARGE syndrome2007 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Familial haemophagocytic lymphohistiocytosis caused by perforin deficit can be successfully treated by haematopoietic stem cell transplantation - the first diagnosed case in the Czech Republic2006 | Second Faculty of Medicine
- Phenotypic profiling of CD34+ cells by advanced flow cytometry improves diagnosis of Juvenile Myelomonocytic Leukemia2024 | Second Faculty of Medicine
- Minimal residual disease assessment in B-cell precursor acute lymphoblastic leukemia by semi-automated identification of normal hematopoietic cells: A EuroFlow study2024 | Second Faculty of Medicine
- CD371+ pediatric B-cell acute lymphoblastic leukemia: propensity to lineage switch and slow early response to treatment2024 | Second Faculty of Medicine
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