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Results: 1-7 |
Results: 7

Authors: Vrablik, M Ceska, R Horinek, A Wichterle, D
Citation: M. Vrablik et al., Absence of the R3531C mutation in the apoB gene in Czech hypercholesterolaemic patients, NUTR MET CA, 11(3), 2001, pp. 212-214

Authors: Vrablik, M Ceska, R Horinek, A
Citation: M. Vrablik et al., Major apolipoprotein B-100 mutations in lipoprotein metabolism and atherosclerosis, PHYSL RES, 50(4), 2001, pp. 337-343

Authors: Stulc, T Ceska, R Horinek, A Stepan, J
Citation: T. Stulc et al., Bone mineral density in patients with apolipoprotein E type 2/2 and 4/4 genotype, PHYSL RES, 49(4), 2000, pp. 435-439

Authors: Ceska, R Vrablik, M Horinek, A
Citation: R. Ceska et al., Familial defective apolipoprotein B-100: a lesson from homozygous and heterozygous patients, PHYSL RES, 49, 2000, pp. S125-S130

Authors: Krsek, M Ceska, R Horinek, A Horejsi, B Weiss, V
Citation: M. Krsek et al., Type III hyperlipoproteinaemia and primary amenorrhoea associated with severe hypothyroidism, ACT PAEDIAT, 89(8), 2000, pp. 1023-1024

Authors: Horejsi, B Spacil, J Ceska, R Vrablik, M Haas, T Horinek, A
Citation: B. Horejsi et al., The independent correlation of the impact of lipoprotein(a) levels and apolipoprotein E polymorphism on carotid artery intima thickness, INT ANGIOL, 19(4), 2000, pp. 331-336

Authors: Horinek, A Ceska, R Sobra, J Vrablik, M
Citation: A. Horinek et al., Familial defective apolipoprotein B-100 homozygote with premature coronaryatherosclerosis. A case report, J INTERN M, 246(2), 1999, pp. 235-236
Risultati: 1-7 |