Publications
- Skin Lesions in a Boy With X-linked Lymphoproliferative Disorder: Comparison of 5 SH2D1A Deletion Cases2012 | 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
- Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)2011 | Second Faculty of Medicine
- Atypical manifestation of severe combined immunodeficiency2011 | Second Faculty of Medicine
- Second national study AML-BFM 98 improved remission rate and overall survival in children with acute myeloid leukemia in the Czech Republic2008 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- 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
- Program of Hematopoietic Stem Cell Transplantation in Children at Department of Pediatric Hematology and Oncology, University Hospital Motol - from Fetal Liver to Cord Blood2007 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Problems in Early Establishment of the Diagnosis of Severe Combined Immunodeficiency2007 | Second Faculty of Medicine, Central Library of Charles University
- 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
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