- Clinical Importance of Identification of PROP1 Gene Mutations in Children with Inherited Growth Hormone Deficiency2009 | Second Faculty of Medicine
- Pituitary Morphology in Patients with Combined Pituitary Hormone Deficiency Due to PROP1 Gene Mutations2005 | Faculty of Physical Education and Sport, First Faculty of Medicine, Third Faculty of Medicine
- Clinical Importance of Identification of PROP1 Gene Mutations in Children with Inherited Growth Hormone Deficiency +12009 | Faculty of Medicine in Hradec Králové
- Clinical Importance of Identification of PROP1 Gene Mutations in Children with Inherited Growth Hormone Deficiency2009 | First Faculty of Medicine
- Morphiology of pituitary gland in patients with multiple pituitary hormone insuficiency in the patients with PROP1 gene mutationPublication without faculty affiliation
- Is genetic testing in children with growth hormone deficiency clinically justified?2013 | Second Faculty of Medicine
- Lucas who likes horses2011 | Second Faculty of Medicine
- Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects2005 | Faculty of Physical Education and Sport, First Faculty of Medicine, Third Faculty of Medicine
- Therapy-Induced Growth and Sexual Maturation in a Developmentally Infantile Adult Patient with a PROP1 Mutation2017 | First Faculty of Medicine, Third Faculty of Medicine, Faculty of Science
- Mutations and Pituitary Morphology in a Series of 82 Patients with PROP1 Gene Defects2011 | Second Faculty of Medicine
- Pituitary size in patients with PROP1 mutations throughout lifespan: from early hyperplasia to late atrophy?Publication without faculty affiliation
- Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes2017 | Second Faculty of Medicine
- Natural growth and response to growth hormone therapy in 18 czech patients with a PROP1 gene defectPublication without faculty affiliation
- Natural growth and response to growth hormone therapy in a population - based cohort of 18 patients with PROP1 gene defectPublication without faculty affiliation
- Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations2016 | Second Faculty of Medicine
- High Prevalence of PROP1 Defects in Lithuania: Phenotypic Findings in an Ethnically Homogenous Cohort of Patients With Multiple Pituitary Hormone Deficiency2014 | Second Faculty of Medicine
- Prevalence of PROP1 gene defects in a population-based cohort of patients with multiple pituitary hormone deficiency and their natural history of growth and response to growth hormone treatmentPublication without faculty affiliation
- Role of transcription factors in pituitary embryogenesis2007 | Third Faculty of Medicine
- Role of transcription factors in pituitary embryogenesis2007 | Second Faculty of Medicine
- Gregor Mendel and regulation of child's growth: genes, molecules, and paediatric clinical routine2022 | Second Faculty of Medicine
- Disorders of pituitary morphogenesis and differentiation2006 | Faculty of Medicine in Hradec Králové, Second Faculty of Medicine, Faculty of Physical Education and Sport, First Faculty of Medicine, Third Faculty of Medicine
- Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes2018 | Second Faculty of Medicine
