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
- Macro AST - cause of asymptomatic aspartate aminotransferase elevation - case report2018 | Third Faculty of Medicine, First Faculty of Medicine
- ACTH dependent Cushing's syndrome - case report2018 | Third Faculty of Medicine
- A product of immunoreactive trypsinogen and pancreatitis-associated protein as second-tier strategy in cystic fibrosis newborn screening2016 | Second Faculty of Medicine, Third Faculty of Medicine
- Diffuse parenchymal lung disease as first clinical manifestation of GATA-2 deficiency in childhood2015 | Second Faculty of Medicine, Third Faculty of Medicine
- Lessons learned from 5 years of newborn screening for congenital adrenal hyperplasia in the Czech Republic: 17-hydroxyprogesterone, genotypes, and screening performance2012 | Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Prospective and parallel assessments of cystic fibrosis newborn screening protocols in the Czech Republic: IRT/DNA/IRT versus IRT/PAP and IRT/PAP/DNA2012 | Second Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University
- The Newborn Screening for Cystic Fibrosis in the Czech Republic: Results of Pilot Study2007 | Second Faculty of Medicine, Third Faculty of Medicine
- Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia2005 | Third Faculty of Medicine
- A boy with adrenal insufficiency and DAX-1 gene defect2001 | 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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