Publications
- A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia2020 | First Faculty of Medicine, Second Faculty of Medicine, Central Library of Charles University, Faculty of Science
- Fanconi anemia in the Czech Republic: Role of HSCT and long-term follow-up2020 | Second Faculty of Medicine
- 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
- Differential diagnosis of anaemia in children2014 | Publication without faculty affiliation
- Immunosuppressive therapy combining anti-thymocyte globulin and cyclosporine A in childhood acquired aplastic anaemia - long term-outcomes and risks2012 | Second Faculty of Medicine
- The role of allogeneic haematopoietic stem cell transplantation in the treatment of acquired aplastic anaemia in children - experience in the Czech Republic from 1991-20072011 | Second Faculty of Medicine
- Significant progress in the treatment of acquired aplastic anemia in children in 1990s1998 | Second Faculty of Medicine, Central Library of Charles University
- Acute haemolytic crisis with hepatic failure as the first manifestation of morbus Wilson in children1996 | Second Faculty of Medicine
- Four Additional Doses of PEG-L-Asparaginase During the Consolidation Phase in the AIEOP-BFM ALL 2009 Protocol Do Not Improve Outcome and Increase Toxicity in High-Risk ALL: Results of a Randomized Study2024 | Second Faculty of Medicine
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