H. Hansíková
-
Novel Mutations in the TAZ Gene in Patients with Barth Syndrome
S. Mazurová, M. Tesařová, M. Magner, H. Houšťková, H. Hansíková, J. Augustínová, V. Tomek, A. Vondráčková, J. Zeman, Tomáš Honzík*
2013, Vol. 114, Issue 3, pp. 139-153 -
Novel Mutations in the Tyrosine Hydroxylase Gene in the First Czech Patient with Tyrosine Hydroxylase Deficiency
K. Szentiványi, H. Hansíková, J. Krijt, K. Vinšová, M. Tesařová, E. Rozsypalová, P. Klement, J. Zeman, Tomáš Honzík
2012, Vol. 113, Issue 2, pp. 136-146
The following name might also represent this author:
Hana Hansíková
-
Hereditary Multiple Exostoses: Clinical, Molecular and Radiologic Survey in 9 Families
Karel Medek, Jiří Zeman, Tomáš Honzík, Hana Hansíková, Štěpánka Švecová, Kamila Beránková, Vendula Kučerová Vidrová, Miloslav Kuklík, Jiří Chomiak, Markéta Tesařová
2017, Vol. 118, Issue 2-3, pp. 87-94 -
Isoelectric Focusing of Serum Apolipoprotein C-III as a Sensitive Screening Method for the Detection of O-glycosylation Disturbances
Nina Ondrušková, Tomáš Honzík, Jitka Kytnarová, Martin Matoulek, Jiří Zeman, Hana Hansíková
2015, Vol. 116, Issue 2, pp. 73-86
