Publications
- Fanconi anemia with biallelic FANCD1/BRCA2 mutations - Case report of a family with three affected children2016 | Second Faculty of Medicine
- Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene - Case Report2016 | Second Faculty of Medicine
- Ikaros (IKZF1) alterations and minimal residual disease at day 15 assessed by flow cytometry predict prognosis of childhood BCR/ABL-negative acute lymphoblastic leukemia2013 | Second Faculty of Medicine
- The adaptor protein NTAL enhances proximal signaling and potentiates corticosteroid-induced apoptosis in T-ALL2012 | Second Faculty of Medicine
- Adaptor molecules PAG, NTAL and LAT in physiological lymphocyte precursors and in childhood leukaemia2009 | Second Faculty of Medicine
- Adaptor molecules expression in normal lymphopoiesis and in childhood leukemia2009 | Second Faculty of Medicine
- The ECHO recommendations for dealing with vinblastine shortage affecting standard treatment of systemic Langerhans cell histiocytosis2024 | Second Faculty of Medicine
- Constitutively active Lyn kinase causes a cutaneous small vessel vasculitis and liver fibrosis syndrome2023 | Second Faculty of Medicine, Central Library of Charles University
- Clinicogenomic associations in childhood Langerhans cell histiocytosis: an international cohort study2023 | Second Faculty of Medicine
- The Role of Cryotherapy in Vitreous Concentrations of Topotecan Delivered by Episcleral Hydrogel Implant2022 | First Faculty of Medicine, Second Faculty of Medicine
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