- Multiple endocrine neoplasia2010 | Second Faculty of Medicine
- Multiple endocrine neoplasia type 2 syndrome2009 | Second Faculty of Medicine
- Multiple endocrine neoplasia in childhood2023 | Faculty of Medicine in Pilsen
- Multiple Endocrine Ne oplasi a Type 2 Syndrome2009 | Central Library of Charles University, Second Faculty of Medicine
- Multiple endocrine neoplasia type 2B: clinical course and outcomes2021 | Faculty of Medicine in Pilsen
- Multiple endocrine neoplasia 2B2004 | Central Library of Charles University, 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
- Multiple endocrine neoplasia type 1 syndrome with special emphasis on pancreatoduodenal tumours - a case report analysis2013 | Publication without faculty affiliation
- Mnohočetná endokrinní neoplazie1997 | Second Faculty of Medicine
- Multiple endocrine neoplasia type 1 at a young woman2014 | Faculty of Medicine in Hradec Králové
- Multiple endocrine neoplasia type 1 - MEN 1 syndrome +12009 | Faculty of Medicine in Hradec Králové
- Multiple Endocrine Neoplasia Type 1 Syndrome2009 | Second Faculty of Medicine
- Multiple endocrine neoplasia type 1 - MEN 1 syndrome2009 | First 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 | 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, First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A2007 | First Faculty of Medicine
- Implication of molecular genetic examination in a Ihree generational family with multiple endoerine neoplasia type 2A2007 | First Faculty of Medicine, Second Faculty of Medicine
- Paraganglioma in a patient with the multiple endocrine neoplasia type I: unusual feature of MEN I, mixed MEN I and MEN II, or MEN IV?2013 | First Faculty of Medicine
- Metastatic insulinoma - a case report of a patient with MEN 1 syndrome2023 | Faculty of Medicine in Hradec Králové
- Hereditary pheochromocytoma and paraganglioma2012 | First Faculty of Medicine
- RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest2009 | First Faculty of Medicine
- Pheochromocytoma2009 | First Faculty of Medicine
- Pheochromocytoma - clinical aspects2009 | First Faculty of Medicine
- Somatostatin receptor PET beyond the neuroendocrine tumors of the gastrointestinal tract - the review of literature2021 | First Faculty of Medicine
- Genetic Causes of the Thyroid Carcinomas2004 | Second Faculty of Medicine
- Hereditary pheochromocytoma and paraganglioma2012 | Central Library of Charles University, Second Faculty of Medicine
- Medullarythyroidcarcinoma - diagnostic a therapeutic alternative2011 | Second Faculty of Medicine
- Hereditary thyroid carcinoma and its molecular diagnostics2014 | Central Library of Charles University