Prague Medical Report
Journal of First Faculty of Medicine, Charles University, Czech Republic 

Individual author index pages

• S. Mazurová
• M. Tesařová
• M. Magner
• H. Houšťková
• H. Hansíková
• J. Augustínová
• V. Tomek
•  A. Vondráčková
• J. Zeman
• Tomáš Honzík

Other articles of these authors

• 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
• 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
• Heart Failure Treated with Low-dose Milrinone in a Full-term Newborn

  S. Šebková, V. Tomek, P. Zemanová, Jan Janota

  2012, Vol. 113, Issue 1, pp. 58-65
• 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