- Spinal Complications in Genetic Syndromes - Case Reports2011 | First Faculty of Medicine
- Spinal Complications in Genetic Syndromes - Case Reports2011 | Publication without faculty affiliation
- Minor anomalies are clues toward the recognition of genetic syndromes2008 | Second Faculty of Medicine
- Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A2007 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport, Central Library of Charles University, Faculty of Medicine in Hradec Králové
- Implication of molecular genetic examination in a Ihree generational family with multiple endoerine neoplasia type 2A2007 | First Faculty of Medicine, Second Faculty of Medicine
- Neurogenetics2013 | First Faculty of Medicine
- The importance of classical cytogenetic examination in clinical paediatric practice: analysis of 384 indications2014 | First Faculty of Medicine
- Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach2023 | Faculty of Physical Education and Sport
- Subsequent neoplasms in childhood cancer survivors2020 | Second Faculty of Medicine
- Complex approach towards patients with hypertrophic cardiomyopathy and indications to genetic testing2020 | Second Faculty of Medicine, Central Library of Charles University
- Noonan syndrom with multiple lentigines and congenital myotonic dystrophy type 1 in a newborn2020 | Faculty of Medicine in Pilsen
- The Survey of Syndromes with the Risk of Cancer in Children Age2009 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Hereditary pheochromocytoma and paraganglioma2012 | First Faculty of Medicine
- Genetic disorders and sleepiness: medical, psychiatric and neurological causes of sleepiness2011 | First Faculty of Medicine
- Hereditary pheochromocytoma and paraganglioma2012 | Second Faculty of Medicine, Central Library of Charles University
- A mutation in the c-Fos gene associated with congenital generalized lipodystrophy2013 | Second Faculty of Medicine
- Gastroesophageal reflux disease in children with psychomotor retardation (PMR)2016 | Second Faculty of Medicine
- Current nomenclature and histopathological criteria for assessment of the noninflammatory degenerative diseases of the aorta2020 | Second Faculty of Medicine
- The most common motor stereotypes in childhood2022 | Publication without faculty affiliation
- Defects of insulin and IGF-1 action at receptor and postreceptor level in a patient with type A syndrome of insulin resistance1997 | Second Faculty of Medicine
- Differential diagnosis of hyperglycemia in children and adolescent2005 | Third Faculty of Medicine
- Current perspectives on the aetiology of tall stature in children and adolescents (1): Syndromes associated with tall stature2022 | Second Faculty of Medicine
- Differential diagnosis of childhood obesity2002 | Third Faculty of Medicine
- Iron chelation in the treatment of neurodegenerative diseases2016 | First Faculty of Medicine
- Radiotherapy and radiosensitivity syndromes in DNA repair gene mutations2022 | First Faculty of Medicine
- Molecules of Life and Mutations: a new course of advanced pathophysiology combining several modern didactic approaches2019 | First Faculty of Medicine, Faculty of Science, Faculty of Medicine in Pilsen
- Acute aortic dissection - an unexpected cause of death of a young pregnant woman. Case report2021 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Overweight and obesity in children and adolescents with endocrine disorders2023 | Faculty of Medicine in Pilsen
- Integrative role of the SALL4 gene: From thalidomide embryopathy to genetic defects of the upper limb, internal organs, cerebral midline, and pituitary2024 | Second Faculty of Medicine
- Autistic and dysphasic children differ in social responsiveness and empathy but not in systemizing behavior2023 | Second Faculty of Medicine