P. Martásek
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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 -
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
The following name might also represent this author:
Pavel Martásek
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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 -
A Novel Mutation in the FECH Gene in a Czech Family with Erythropoietic Protoporphyria and a Population Study of IVS3-48C Variant Contributing to the Disease
M. S. Farrag, J. Kučerová, L. Šlachtová, O. Šeda, J. Šperl, Pavel Martásek
2015, Vol. 61, Issue 6, pp. 227-232 -
Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients
M. S. Farrag, I. Mikula, E. Richard, V. Saudek, H. De Verneuil, Pavel Martásek
2015, Vol. 61, Issue 6, pp. 219-226 -
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
