V. Stránecký
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Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case
B. Kousal, T. Honzík, H. Hansíková, N. Ondrušková, A. Čechová, M. Tesařová, V. Stránecký, M. Meliška, M. Michaelides, Petra Lišková
2019, Vol. 65, Issue 3, pp. 134-141 -
Lipoprotein Lipase Deficiency: Clinical, Biochemical and Molecular Characteristics in Three Patients with Novel Mutations in the LPL Gene
H. Kolářová, M. Tesařová, Š. Švecová, V. Stránecký, A. Přistoupilová, T. Zima, J. Uhrová, S. Y. Volgina, J. Zeman, Tomáš Honzík
2014, Vol. 60, Issue 5, pp. 235-243
