Hereditary defect of apolipoprotein B 100 – analysis of group of patients treated with standard peroral lipid-lowering therapy in St. Anne's University Hospital Brno by Kyselak, O, Soska, V

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Achieving target lipid levels in patients with familial hypercholesterolaemia in clinical practice by Kyselak, O., Soska, V.

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Child With Familial Hypercholesterolemia Phenotype by Kyselak, O., Soska, V.

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Different phenotypes in siblings with heterozygous familial hypercholesterolemia by Kyselak, O., Soska, V.

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Analysis of hypertriglyceridemic gene score in patients with familial dysbetalipoproteinemia by Satny, M., Todorovova, V., Vrablík, M., Hubacek, J., Altschmiedova, T., Soska, V., Kyselak, O.

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Performance of various diagnostic criteria of familial dysbetalipoproteinemia in ApoE2/E2 homozygotes with mixed dyslipidaemia by Satny, M., Vrablik, M., Altschmiedova, T., Todorovová, V., Soska, V., Kyselak, O.

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General characteristics of pacients with homozygous form of familial hypercholesterolaemia in the Czech Republic by Tesarova, S., Blaha, V., Ceska, R., Dvorakova, J., Freiberger, T., Horak, P., Hyanek, J., Kyselak, O., Nussbaumerova, B., Soska, V., Urbanek, R., Vaclova, M., Vaverkova, H., Vrablik, M., Vyroubal, P., Zemek, S., Zlatohlavek, L.

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Determination of hypertriglyceridemic gene score in patients with familial dysbetalipoproteinemia by Satny, MS, Vrablik, MV, Altschmiedova, TA, Todorovova, VT, Hubacek, JH, Kyselak, OK, Soska, VS

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