Publications
- Molecular Diagnostics of Copper-Transporting Protein Mutations Allows Early Onset Individual Therapy of Menkes Disease2017 | First Faculty of Medicine
- The Prediction of Coronary Artery Disease Based on Non-Invasive Examinations and Heme Oxygenase 1 Polymorphism Versus Virtual Histology2013 | First Faculty of Medicine, Faculty of Education
- Stress Perception and (GT)n Repeat Polymorphism in Haem Oxygenase 1 Promoter Are Both Risk Factors in Development of Eating Disorders2013 | First Faculty of Medicine, Faculty of Education
- Prediction of coronary vessel involvement on the basis of atherosclerosis risk factor analysis2013 | First Faculty of Medicine
- Microsatellite Polymorphism in Haem Oxygenase 1 Gene Promoter in Multiple Sclerosis2012 | First Faculty of Medicine
- Genetic Variants in Haem Oxygenase-1 and Endothelial Nitric Oxide Synthase Influence the Extent and Evolution of Coronary Artery Atherosclerosis2011 | First Faculty of Medicine
- Mutations in genes coding for ATP7A and ATP7B (causing Mankes and Wilson disease) in Czech RepublicPublication without faculty affiliation
- Mutation Screening in the ATP7A and ATP7B Genes in Czech patients with Menkes Disease and Wilson DiseasePublication without faculty affiliation
- Molecular pathology of Menkes and Wilson diseases in Czech RepublicPublication without faculty affiliation
- Study of the association of a promoter polymorphism in the heme oxygenase-1 gene with multiple sclerosisPublication without faculty affiliation
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