- Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects2005 | First Faculty of Medicine, Faculty of Physical Education and Sport, Third Faculty of Medicine
- A boy with adrenal insufficiency and DAX-1 gene defect2001 | Third 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
- Mutations and Pituitary Morphology in a Series of 82 Patients with PROP1 Gene Defects2011 | Second Faculty of Medicine
- SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Léri-Weill dyschondrosteosis2012 | Faculty of Science, First Faculty of Medicine
- SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Leri-Weill dyschondrosteosis2012 | First Faculty of Medicine
- Mutations and polymorphisms porphobilinogen deaminase gene: Defects which result in acute intermittent porphyria: May 2006 update with the list of mutations in Slavic population2006 | First Faculty of Medicine
- Mutations and polymorphisms porphobilinogen deaminase gene: Defects which result in acute intermittent porphyria: May 2006 update with the list of mutations in Slavic population2006 | Faculty of Physical Education and Sport
- Characterization of 13 Novel Band 3 Gene Defects in Hereditary Spherocytosis With Band 3 Deficiency1996 | Faculty of Medicine in Hradec Králové
- Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population2016 | First Faculty of Medicine
- Disorders of sex differentiation: genes responsible for development of genital system and final phenotype2009 | Second Faculty of Medicine
- anamnézy; defekt jednoho genu2006 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport, Third Faculty of Medicine, Central Library of Charles University
- Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype: case report2017 | First Faculty of Medicine, Second Faculty of Medicine
- Six novel mutations in the GCK gene in MODY patients2007 | Third 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
- Discovery of gene causing congenital anomalies of urinary tract2013 | First Faculty of Medicine
- The relationship of the expression of mismatch repair (MLH1, MSH2) proteins to colonic adenomas2005 | Faculty of Physical Education and Sport
- Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness2017 | First Faculty of Medicine
- Congenital myasthenic sydromes2010 | First Faculty of Medicine
- Monogenic forms of diabetes: they are more common than we have thought so far2014 | Second Faculty of Medicine
- Hemiplegic migraine2017 | Publication without faculty affiliation
- Pioglitazone2007 | First Faculty of Medicine
- Pitfalls and drawbacks in screening of congenital disorders of glycocylation2004 | First Faculty of Medicine
- Present International Projects in the Area of Diagnostics and Therapy of Cystic Fibrosis: Participation of Specialists from the Czech Republic into the Problem Solving2008 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Congenital disorders of glycosylation: Still "hot" in 20202021 | First Faculty of Medicine
- Whole-body magnetic resonance imaging in pediatric oncology - recommendations by the Oncology Task Force of the ESPR2020 | Second Faculty of Medicine
- Is genetic testing in children with growth hormone deficiency clinically justified?2013 | Second Faculty of Medicine
- Germline Variants of CYBA and TRPM4 Predispose to Familial Colorectal Cancer2022 | Faculty of Medicine in Pilsen
- Monogenic form of autoimmune diabetes as a part of dysregulation of immune system2018 | Second Faculty of Medicine