Publications
- Fanconi anemia with biallelic FANCD1/BRCA2 mutations - Case report of a family with three affected children2016 | Second Faculty of Medicine
- A pilot study conducted in the Czech Republic relating to the molecular analysis of the RET and GDNF genes in patients with cakut, predominantly unilateral renal agenesis2015 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Current views on cell metabolism in SDHx-related pheochromocytoma and paraganglioma2014 | Second Faculty of Medicine
- Pacak-Zhuang Syndrome: A New Kid on The Block2014 | Second Faculty of Medicine
- Genetics of pheochromocytoma and paraganglioma syndromes: new advances and future treatment options2013 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Hereditary pheochromocytoma and paraganglioma2012 | Second Faculty of Medicine, Central Library of Charles University
- Molecular Cytogenetic Characterization in Four Pediatric Pheochromocytomas and Paragangliomas2011 | Faculty of Science, First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Molecular Cytogenetic Characterization in Four Pediatric Pheochromocytomas and Paragangliomas2011 | Second Faculty of Medicine
- Molecular cytogenetic characterization of pheochromocytoma2010 | Faculty of Science, First Faculty of Medicine, Second Faculty of Medicine, Faculty of Mathematics and Physics, Faculty of Physical Education and Sport
- Paraganglioma in a 13-year-old girl: A novel SDHB gene mutation in the family?2010 | Faculty of Science, First Faculty of Medicine, Second Faculty of Medicine
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