Fol. Biol. 2012, 58, 69-74
https://doi.org/10.14712/fb2012058020069
Microsatellite Polymorphism in Haem Oxygenase 1 Gene Promoter in Multiple Sclerosis
Individual author index pages
Other articles of these authors
-
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 -
Novel CDKL5 Mutations in Czech Patients with Phenotypes of Atypical Rett Syndrome and Early-Onset Epileptic Encephalopathy
Daniela Záhoráková, M. Langová, K. Brožová, J. Laštůvková, Z. Kalina, L. Rennerová, P. Martásek
2016, Vol. 62, Issue 2, pp. 67-74 -
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 -
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 -
Apolipoprotein E ε4-Positive Multiple Sclerosis Patients Develop More Gray-Matter and Whole-Brain Atrophy: a 15-Year Disease History Model Based on a 4-Year Longitudinal Study
Dana Horáková, M. Kýr, E. Havrdová, O. Doležal, P. Lelková, L. Pospíšilová, N. Bergsland, M. G. Dwyer, J. L. Cox, S. Hussein, Z. Seidl, M. Vaněčková, J. Krásenský, R. Zivadinov
2010, Vol. 56, Issue 6, pp. 242-251