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
- Novel Mutations in the Tyrosine Hydroxylase Gene in the First Czech Patient with Tyrosine Hydroxylase Deficiency2012 | First Faculty of Medicine
- Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 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
- Elevated CSF-lactate is a reliable marker of mitochondrial disorders in children even after brief seizures2011 | Faculty of Science, First Faculty of Medicine
- The importance of biogenic amines metabolities determination in cerebrospinal fluid by high performance liquid chromatography in the diagnostics of pediatric neurotransmitter disorders.2011 | First Faculty of Medicine
- Elevated CSF-lactate is a reliable marker of mitochondrial disorders in children even after brief seizures2011 | First Faculty of Medicine
- Clinical manifestations of inherited metabolic disorders in childhood2011 | First Faculty of Medicine
- Elevated lactate is a reliable marker pointing to mitochondrial disorders even in children after brief seizures.2010 | Faculty of Science, Faculty of Physical Education and Sport, First Faculty of Medicine
- Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal development2010 | 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
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