Publications
- Novel Mutations in the Tyrosine Hydroxylase Gene in the First Czech Patient with Tyrosine Hydroxylase Deficiency2012 | First Faculty of Medicine
- Sco2 Protein Deficiency-Based Mitochondrial Encephalomyopathy with the SMA-like Picture of Neurogenic Muscle Atrophy - Case Reports2010 | First Faculty of Medicine
- Methylmalonic Acidemia : clinical, biochemical a molecular biological studie2006 | First Faculty of Medicine
- Methylmalonic Acidemia : clinical, biochemical a molecular biological studie2006 | Faculty of Physical Education and Sport
- Altered properties of mitochondrial ATP-synthase in patients with a T --> G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA1995 | First Faculty of Medicine
- Long term Follow up of Prematurely Born Child: When Does It Start and When Does It End?2020 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Second Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine
- Testové otázky z pediatrie2020 | First Faculty of Medicine, Second Faculty of Medicine
- Severity of asphyxia is a covariate of phenobarbital clearance in newborns undergoing hypothermia2019 | First Faculty of Medicine
- Neonatal Onset of Epilepsy of Infancy with Migrating Focal Seizures Associated with a Novel GABRB3 Variant in Monozygotic Twins2018 | Second Faculty of Medicine
- Diagnostics and treatment of children with acute seizures on paediatric intensive care unit2018 | First Faculty of Medicine
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