Publications
- Iron status in patients with pyruvate kinase deficiency: neonatal hyperferritinaemia associated with a novel frameshift deletion in the PKLR gene (p.Arg518fs), and low hepcidin to ferritin ratios2014 | Publication without faculty affiliation
- Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopenia2013 | Second Faculty of Medicine
- SNP Array and Phenotype Correlation Shows That FLI1 Deletion Per se is Not Responsible for Thrombocytopenia Development in Jacobsen Syndrome2012 | Publication without faculty affiliation
- 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
- Secondary hemophagocytic lymphohistiocytosis in SARS-CoV-2 infection2022 | Second Faculty of Medicine
- Czech and Slovak Diamond-Blackfan Anemia (DBA) Registry update: Clinical data and novel causative genetic lesions2020 | Central Library of Charles University
Loading network view...