- Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A2007 | Faculty of Medicine in Hradec Králové, Central Library of Charles University
- Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A2007 | Faculty of Medicine in Hradec Králové, Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Implication of molecular genetic examination in a Ihree generational family with multiple endoerine neoplasia type 2A2007 | First Faculty of Medicine, Second Faculty of Medicine
- Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A2007 | Faculty of Medicine in Hradec Králové
- Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A2007 | First Faculty of Medicine
- Hereditary thyroid carcinoma and its molecular diagnostics2014 | Central Library of Charles University
- Multiple endocrine neoplasia2010 | Second Faculty of Medicine
- Neuroendocrine tumors in cases2018 | First Faculty of Medicine
- The penetrance of MEN2 pheochromocytoma is not only determined by RET mutations2017 | First Faculty of Medicine, Second Faculty of Medicine
- Screening of six risk exons of the RET proto-oncogene in families with medullary thyroid carcinoma in the Czech Republic2004 | Second Faculty of Medicine
- Multiple Endocrine Neoplasia I (Wermer's Syndrome), Forms of Clinical Manifestation, 5 Case Studies2016 | First Faculty of Medicine, Second Faculty of Medicine
- RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest2009 | Second Faculty of Medicine
- RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest2009 | Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine