Classes
- Paediatrics +3B00219 | First Faculty of Medicine
- Nursing in PaediatricsB00256 | First Faculty of Medicine
- Nursing in Paediatrics 2 DB00542 | First Faculty of Medicine
- Nursing in Paediatrics 1 DB00545 | First Faculty of Medicine
- Pediatric Nursing +1B01799 | First Faculty of Medicine
- Pediatrics with a focus on nutritionB02285 | First Faculty of Medicine
- Pediatrics +1B02471 | First Faculty of Medicine
Publications
- Novel Mutations in the TAZ Gene in Patients with Barth Syndrome2013 | First Faculty of Medicine
- Vitamin B 12 deficiency in breastfed infants-treatable cause of psychomotor retardation: etiology, clinical signs and laboratory findings2008 | First Faculty of Medicine
- Retrospective, multicentric study of 180 children with cytochrome c oxidase deficiency2006 | First Faculty of Medicine
- Deficiency of mitochondrial ATP synthase of nuclear genetic origin2006 | First Faculty of Medicine
- Retrospective, multicentric study of 180 children with cytochrom C oxidase deficiency2006 | Faculty of Physical Education and Sport
- Deficiency of mitochondrial ATP synthase of nuclear genetic origin2006 | Faculty of Physical Education and Sport
- A Novel Mutation in SURF1 Causes Skipping of Exon 8 in a Patient with Cytochrome c Oxidase-Deficient Leigh Syndrome and Hypertrichosis2001 | First Faculty of Medicine
- Two components in pathogenic mechanism of mitochondrial ATP synthase deficiency: energy deprivation and ROS productionPublication without faculty affiliation
- Isolated deficiency of mitochondrial ATP synthase caused by nuclear genetic originPublication without faculty affiliation
- Isolated deficiency of mitochondrial ATP synthase caused by nuclear genetic defectsPublication without faculty affiliation
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