Classes
- 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
- Curriculum of Paediatrics before State ExaminationB81057 | First Faculty of Medicine
Publications
- Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency2012 | First Faculty of Medicine
- Two Patients with Clinically Distinct Manifestation of Pyruvate Dehydrogenase Deficiency Due to Mutations in PDHA1 Gene2011 | First Faculty of Medicine
- Clinical manifestations of inherited metabolic disorders in childhood2011 | First Faculty of Medicine
- Myoclonic Epilepsy and Deafness in Siblings with the 7512T>C Mutation in the Mitochondrial Encoded tRNA(Ser(UCN)) Gene - Case Reports2010 | Faculty of Science, Faculty of Physical Education and Sport, First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal development2010 | First Faculty of Medicine
- Myoclonic Epilepsy and Deafness in Siblings with the 7512T > C Mutation in the Mitochondrial Encoded tRNA(Ser(UCN)) Gene - Case Reports2010 | First Faculty of Medicine
- Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated FIFo ATP synthase deficiency2008 | First Faculty of Medicine
- Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates2008 | First Faculty of Medicine
- Hepatocellular carcinoma in an infant with tyrosinemia type 12023 | First Faculty of Medicine, Second Faculty of Medicine
- Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes +12023 | Faculty of Science, First Faculty of Medicine
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