- Nonsmall cell lung cancer with RET gene fusion2021 | Publication without faculty affiliation
- Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas +12008 | First Faculty of Medicine
- Thyroid carcinomas and Hirschsprung's disease - 10-year experience with molecular genetic testing of the RET proto-oncogene2006 | Second Faculty of Medicine
- Thyroid carcinomas and Hirschsprung's disease - 10-year experience with molecular genetic testing of the RET proto-oncogene2006 | Central Library of Charles University, Second Faculty of Medicine
- RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest2009 | First Faculty of Medicine
- Double Germline Mutations in the RET Proto-oncogene in MEN 2A and MEN 2B Kindreds2006 | Publication without faculty affiliation
- Double Germline Mutations in the RET Proto-oncogene in MEN 2A and MEN 2B Kindreds2006 | First Faculty of Medicine
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg2005 | First Faculty of Medicine
- Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas2008 | Faculty of Medicine in Hradec Králové
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg2005 | Faculty of Medicine in Hradec Králové
- Detection of Minimal Residual Disease in Ewing's sarcoma Using RT-PCR2000 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- New multiple somatic mutations in the RET proto-oncogene associated with a sporadic medullary thyroid carcinoma2007 | First Faculty of Medicine
- Thyroid tumors - moleculargenetic causes and choices for target therapy2012 | Central Library of Charles University
- RET protooncogene mutations in patients with medullary thyroid carcinomaPublication without faculty affiliation
- Genetics of Thyroid Cancer and its Molecular Target Therapy2011 | Central Library of Charles University
- RET fusion genes in pediatric and adult thyroid carcinomas: cohort characteristics and prognosis2023 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- Double Germline Mutations in the RET Proto-oncogene in MEN 2A and MEN 2B Kindreds2006 | Faculty of Medicine in Hradec Králové
- 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 | First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine
- A novel RET/PTC variant detected in a pediatric patient with papillary thyroid cancer without ionization history2015 | First Faculty of Medicine, Faculty of Science, Second Faculty of Medicine
- Medullarythyroidcarcinoma - diagnostic a therapeutic alternative2011 | Second Faculty of Medicine
- RT-CGMS (real time continuous glucose monitoring system) using in the care of newborns of diabetic mothers2015 | 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, 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 Ihree generational family with multiple endoerine neoplasia type 2A2007 | First Faculty of Medicine, Second Faculty of Medicine
- Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas2008 | Faculty of Medicine in Hradec Králové, Central Library of Charles University
- Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas2008 | 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
- RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease2014 | Central Library of Charles University
- Hirschsprung's disease and its genetic cause2013 | Faculty of Science, Second Faculty of Medicine
- Double germline mutations in the RET proto-oncogene in MEN 2A and MEN 2B kindreds2006 | Second Faculty of Medicine