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

Individual author index pages

• Anna Čechová
• Alice Baxová
• Jiří Zeman
• Lukáš Lambert
• Tomáš Honzík
• Alena Leiská
• Václav Čunát
• Markéta Tesařová

Other articles of these authors

• 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
• 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
• Juxtarenal Mycotic Aneurysm as a Complication of Acute Exacerbation of Chronic Cholecystitis Treated by Resection and Replacement by a Fresh Allograft

  Tomáš Grus, Lukáš Lambert, Vilém Rohn, Tomáš Klika, Gabriela Grusová, Pavel Michálek

  2016, Vol. 117, Issue 1, pp. 54-60
• Budd-Chiari Syndrome

  Tomáš Grus, Lukáš Lambert, Gabriela Grusová, Rohan Banerjee, Andrea Burgetová

  2017, Vol. 118, Issue 2-3, pp. 69-80
• 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
• The Age Dependent Progression of Hajdu-Cheney Syndrome in Two Families

  Jitka Jirečková, Martin Magner, Lukáš Lambert, Alice Baxová, Alena Leiská, Lenka Kopečková, Lenka Fajkusová, Jiří Zeman

  2018, Vol. 119, Issue 4, pp. 156-164
• 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