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
- 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
- The Global Retinoblastoma Outcome Study: a prospective, cluster-based analysis of 4064 patients from 149 countries2022 | Second Faculty of Medicine
- Paediatric Nephrology2021 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Is There a Higher Incidence of Sporadic Renal Angiomyolipoma in Childhood Cancer Survivors?2021 | Second Faculty of Medicine, Faculty of Medicine in Pilsen
- Travel burden and clinical presentation of retinoblastoma: analysis of 1024 patients from 43 African countries and 518 patients from 40 European countries2021 | Second Faculty of Medicine
Loading network view...