- Pediatric Case of Primary Cutaneous Eosinophil-Rich CD30 Anaplastic Large-Cell Lymphoma With Follicular Mucinosis2014 | Faculty of Medicine in Pilsen
- Case reports (not only) from primary pediatric practice III.2023 | Second Faculty of Medicine
- Narcolepsy in childhood2009 | First Faculty of Medicine
- Narcolepsy in childhood2009 | Publication without faculty affiliation
- TB meningitis in the Czech Republic - new encounter with an old diagnosis after 20 years2016 | First Faculty of Medicine
- Oral Ibandronate Therapy in Three Patients with Osteogenesis Imperfecta2021 | Faculty of Medicine in Hradec Králové, Third Faculty of Medicine
- Cerebral sinovenous thrombosis in children with nephrotic syndrome: systematic review and one new case2023 | Second Faculty of Medicine
- Mixed Epithelial and Stromal Tumor of the Kidney: Mutation Analysis of the DICER 1 Gene in 29 Cases2017 | Faculty of Medicine in Pilsen
- Rearrangement of KMT2A Characterizes a Subset of Pediatric Parotid Mucoepidermoid Carcinomas Arising Metachronous to Acute Lymphoblastic Leukemia2023 | Faculty of Medicine in Pilsen
- Relapsing encephalopathy with cerebellar ataxia are caused by variants involving p.Arg756 in ATP1A32019 | First Faculty of Medicine
- Complication rates in rigid vs. flexible endoscopic foreign body removal in children2023 | Second Faculty of Medicine
- A subset of pediatric-type thalamic gliomas share a distinct DNA methylation profile, H3K27me3 loss and frequent alteration of EGFR2021 | Second Faculty of Medicine
- Idiopathic vs. secondary retroperitoneal fibrosis: a clinicopathological study of 12 cases, with emphasis to possible relationship to IgG4-related disease2013 | Faculty of Medicine in Hradec Králové
- Surgical management of major pancreatic injury in children2007 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Genome-wide peripheral blood leukocyte DNA methylation microarrays identified a single association with inflammatory bowel diseases2012 | Second Faculty of Medicine
- Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood2022 | Second Faculty of Medicine
- Dystonia Linked to EIF4A2 Haploinsufficiency: A Disorder of Protein Translation Dysfunction2023 | First Faculty of Medicine