H. Hansíková
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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 -
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
The following name might also represent this author:
Hana Hansíková
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Stable COX17 Downregulation Leads to Alterations in Mitochondrial Ultrastructure, Decreased Copper Content and Impaired Cytochrome c Oxidase Biogenesis in HEK293 Cells
M. Vanišová, D. Burská, J. Křížová, T. Daňhelovská, Ž. Dosoudilová, J. Zeman, L. Stibůrek, Hana Hansíková
2019, Vol. 65, Issue 4, pp. 181-187 -
Buccal Respiratory Chain Complexes I and IV Quantities in Huntington’s Disease Patients
P. Dušek, M. Rodinová, I. Lišková, J. Klempíř, J. Zeman, J. Roth, Hana Hansíková
2018, Vol. 64, Issue 1, pp. 31-34 -
Non-Invasive Screening of Cytochrome c Oxidase Deficiency in Children Using a Dipstick Immunocapture Assay
M. Rodinová, E. Trefilová, T. Honzík, M. Tesařová, J. Zeman, Hana Hansíková
2014, Vol. 60, Issue 6, pp. 268-274
