Classes
- Curriculum of Paediatrics before State ExaminationB81057 | First Faculty of Medicine
- PaediatricsB00141 | First Faculty of Medicine
- Propaedeutics in Paediatrics - Summer PracticeB00609 | First Faculty of Medicine
- Propaedeutics in Paediatrics +2B00610 | First Faculty of Medicine
- Paediatrics Practice before State ExaminationB01057 | First Faculty of Medicine
- Paediatrics - Summer Practice +1B03304 | First Faculty of Medicine
- Pediatric Nursing 1B03453 | First Faculty of Medicine
- Paediatric Nursing 2B03468 | First Faculty of Medicine
- Paediatrics SEB80141 | First Faculty of Medicine
Publications
- Importance of early diagnostics of inherited metabolic disorders in neonatal age2013 | First Faculty of Medicine
- Novel Mutations in the Tyrosine Hydroxylase Gene in the First Czech Patient with Tyrosine Hydroxylase Deficiency2012 | First Faculty of Medicine
- Neonatal onset of mitochondrial disorders in 129 patients: clinical and laboratory characteristics and a new approach to diagnosis2012 | First Faculty of Medicine
- Clinical symptoms and laboratory data in 75 children with neonatal manifestation of mitochondrial disease: Proposed diagnostics algorithms2010 | First Faculty of Medicine
- Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation2010 | First Faculty of Medicine
- A new case of ALG8 deficiency (CDG Ih)2009 | First Faculty of Medicine, Third Faculty of Medicine
- TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy2008 | First Faculty of Medicine
- Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates2008 | First Faculty of Medicine
- Effect of a novel intronic FBN1 mutation on splicing revealed by splicing minigene assayPublication without faculty affiliation
- Hepatocellular carcinoma in an infant with tyrosinemia type 12023 | First Faculty of Medicine, Second Faculty of Medicine
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