Classes
- Pediatrics, gynecology and obstetrics +1C4VL008 | Third Faculty of Medicine
- Paediatrics - I.C5VL005 | Third Faculty of Medicine
- Peadiatrics II. +1C6VL001 | Third Faculty of Medicine
- ERASMUS - Practice - PaediatricsCERA0P0022 | Third Faculty of Medicine
- ERASMUS - Pediatrics, gynecology and obstetrics - summerCERA4P0051 | Third Faculty of Medicine
- ERASMUS - Pediatrics, gynecology and obstetrics - winterCERA4P0055 | Third Faculty of Medicine
- ERASMUS - Paediatrics - I.CERA5P0081 | Third Faculty of Medicine
- ERASMUS - Module of Paediatrics - Peadiatrics II.CERA6P0056 | Third Faculty of Medicine
- Clinical Medicine Basics V. - Pediatrics, GerontologyCNT053P3 | Third Faculty of Medicine
- Module of Paediatrics - Paediatrics - I.CPADXX35 | Third Faculty of Medicine
Publications
- Procedure in the suspected case of the 21-hydroxylase deficiency detected in Czech newborn screening2017 | Third Faculty of Medicine
- Prenatal and postnatal development of the adrenal glands and adrenal steroid synthesis: effect on newborn screening for congenital adrenal hyperplasia2012 | Second Faculty of Medicine, Third Faculty of Medicine
- Genetic analysis of the CYP21A2 gene in neonatal dried blood spots from children with transiently elevated 17-hydroxyprogesterone2012 | Second Faculty of Medicine, Third Faculty of Medicine
- Chimeric CYP21A1P/CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia2011 | Third Faculty of Medicine, Central Library of Charles University
- Identification of CYP21A2 mutant alleles in Czech patients with 21-hydroxylase deficiency2010 | Second Faculty of Medicine, Third Faculty of Medicine
- Substitution in the promoter region ofthe CYP21 affects a phenotype ofthe disease in patients with 21-hydroxylase deficiency2009 | Third Faculty of Medicine
- Prevalence of congenital adrenal hyperplasia among sudden infant death in the Czech Republic and Austria2007 | Second Faculty of Medicine, Third Faculty of Medicine
- Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia2005 | Second Faculty of Medicine, Third Faculty of Medicine
- Lessons From 30 Years of Clinical Diagnosis and Treatment of Congenital Adrenal Hyperplasia in Five Middle European Countries2001 | Third Faculty of Medicine
- Newborn screening-detected 21-hydroxylase deficiency: growth pattern is not associated with the genotype2024 | Second Faculty of Medicine, Third Faculty of Medicine
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