- Brachytelephalangic Chondrodysplasia Punctata With Distinctive Phenotype and Normal Karyotype1998 | Central Library of Charles University, Faculty of Medicine in Hradec Králové
- Brachytelephalangic Chondrodysplasia Punctata With Distinctive Phenotype and Normal Karyotype.1998 | Faculty of Physical Education and Sport
- Normal karyotype is a poor prognostic factor in myeloid leukemia of Down syndrome: a retrospective, international study2014 | Publication without faculty affiliation
- Molecular Analysis of Chromosome 21 in a Patient With a Phenotype of Down Syndrome and Apparently Normal Karyotype1996 | Second Faculty of Medicine
- Standard Dose Chemotherapy 3+7 Induces Complete Remission in Patients Over 80 Years Old with Single-Lineage Acute Myeloid Leukemias and Normal KaryotypePublication without faculty affiliation
- Pre-transplant Quantitative Determination of NPM1 Mutation Significantly Predicts Outcome of AIlogeneic Hematopoietic Stem Cell Transplantation in Patients with Normal Karyotype AML in Complete Remission2016 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- From cryptic chromosomal lesions to pathologically relevant genes: Integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype2012 | First Faculty of Medicine
- Allogeneic hematopoietic cell transplantation in acute myeloid leukemia with normal karyotype and isolated Nucleophosmin-1 (NPM1) mutation: outcome strongly correlates with disease status2016 | Faculty of Medicine in Pilsen
- Outcome of patients with distinct molecular genotypes and cytogenetically normal AML after allogeneic transplantation2015 | Faculty of Medicine in Pilsen
- Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia2009 | Second Faculty of Medicine
- Patients older than 80 years with de novo acute myeloid leukemias without erythroblastic and/or megakaryocytic dysplasia achieve complete remission and longer survival after classical chemotherapy 3 + 72010 | First Faculty of Medicine
- Localization of AML-related nucleophosmin mutant depends on its subtype and is highly affected by its interaction with wild-type NPM2017 | Central Library of Charles University
- Baseline immunophenotypic profile of bone marrow leukemia cells in acute myeloid leukemia with nucleophosmin-1 gene mutation: a EuroFlow study2023 | Second Faculty of Medicine
- Differentiating juvenile myelomonocytic leukemia from infectious disease - Response1998 | Second Faculty of Medicine
- Diagnostic utility of flow cytometry in myelodysplastic syndrome (single centre experience)2017 | Publication without faculty affiliation
- Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndrome2021 | Second Faculty of Medicine
- Heterochromatin variants of chromosome 9: clinical aspects and method of molecular cytogenetic examinationPublication without faculty affiliation
- Refractory anemia in childhood: a retrospective analysis of 67 patients with particular reference to monosomy 72003 | Second Faculty of Medicine
- Prenatal phenotype of RASopathies2020 | Publication without faculty affiliation
- Scalp Defect (Giant Aplasia Cutis Congenita of the Scalp in a Newborn)2015 | Faculty of Medicine in Hradec Králové
- Recurrent Pregnancy Loss in Two Patients with High Density of NK Cells CD56 and CD16 in Ovulatory Cervical Mucus and in Endometrium (Case Report)2019 | Faculty of Medicine in Pilsen
- AML-associated mutation of nucleophosmin compromises its interaction with nucleolin2018 | Central Library of Charles University
- HOX Gene Expression in Phenotypic and Genotypic Subgroups and Low HOXA Gene Expression as an Adverse Prognostic Factor in Pediatric ALL2010 | Faculty of Science, Second Faculty of Medicine
- Heterochromatin variants of human chromosome 9 and the reproduction failurePublication without faculty affiliation
- Array comparative genome hybridization in patients with developmental delay: two example cases2012 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Array comparative genome hybridization in patients with developmental delay: two example casesPublication without faculty affiliation
- Premature chromosome condensation in humans associated with microcephaly and mental retardation: A novel autosomal recessive condition2002 | Central Library of Charles University
- Development of humanized culture medium with plant-derived serum replacement for human pluripotent stem cells2010 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Differentially expressed miRNAs in trisomy 21 placentas2016 | First Faculty of Medicine
- Bone marrow immunophenotyping by flow cytometry in refractory cytopenia of childhood2015 | Second Faculty of Medicine