Prague Med. Rep. 2012, 113, 136-146
https://doi.org/10.14712/23362936.2015.28
Novel Mutations in the Tyrosine Hydroxylase Gene in the First Czech Patient with Tyrosine Hydroxylase Deficiency
Individual author index pages
- K. Szentiványi
- H. Hansíková
- J. Krijt
- K. Vinšová
- M. Tesařová
- E. Rozsypalová
- P. Klement
- J. Zeman
- Tomáš Honzík
Other articles of these authors
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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 -
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 -
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 -
Attenuated Type of Asphyxiating Thoracic Dysplasia due to Mutations in DYNC2H1 Gene
Anna Čechová, Alice Baxová, Jiří Zeman, Lukáš Lambert, Tomáš Honzík, Alena Leiská, Václav Čunát, Markéta Tesařová
2019, Vol. 120, Issue 4, pp. 124-130 -
Age Dependent Progression of Multiple Epiphyseal Dysplasia and Pseudoachondroplasia Due to Heterozygous Mutations in COMP Gene
Nabil El-Lababidi, Marie Zikánová, Alice Baxová, Lenka Nosková, Alena Leiská, Lukáš Lambert, Tomáš Honzík, Jiří Zeman
2020, Vol. 121, Issue 3, pp. 153-162
