L. Králík
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Molecular Diagnostics of Copper-Transporting Protein Mutations Allows Early Onset Individual Therapy of Menkes Disease
L. Králík, E. Flachsová, H. Hansíková, V. Saudek, J. Zeman, Pavel Martásek
2017, Vol. 63, Issue 5-6, pp. 165-173 -
Stress Perception and (GT)n Repeat Polymorphism in Haem Oxygenase 1 Promoter Are Both Risk Factors in Development of Eating Disorders
L. Šlachtová, D. Kaminská, M. Chvál, L. Králík, Pavel Martásek, H. Papežová
2013, Vol. 59, Issue 6, pp. 233-239 -
Microsatellite Polymorphism in Haem Oxygenase 1 Gene Promoter in Multiple Sclerosis
Pavlína Zborníková, L. Králík, P. Lelková, T. Kalinčík, E. Havrdová, P. Martásek
2012, Vol. 58, Issue 2, pp. 69-74 -
Genetic Variants in Haem Oxygenase-1 and Endothelial Nitric Oxide Synthase Influence the Extent and Evolution of Coronary Artery Atherosclerosis
Aleš Král, T. Kovárník, L. Králík, H. Skalická, J. Horák, G. S. Mintz, J. Uhrová, M. Sonka, A. Wahle, R. Downe, M. Aschermann, P. Martásek, A. Linhart
2011, Vol. 57, Issue 5, pp. 182-190