| Novel insights into genetics and clinics of the HNF1A-MODY T Valkovicova, M Skopkova, J Stanik, D Gasperikova Endocrine regulations 53 (2), 110-134, 2019 | 89 | 2019 |
| Clinical implications of the glucokinase impaired function–Gck-Mody today J Hulín, M Škopková, T Valkovičová, S Mikulajova, M Rosoľanková, ... Physiological Research 69 (6), 995, 2020 | 25 | 2020 |
| Diabetes treatment in two pregnant women with permanent neonatal diabetes mellitus due to a KCNJ11 mutation J Stanik, L Barak, A Dankovcikova, T Valkovicova, M Skopkova, ... Diabetic Medicine 37 (11), 1956-1958, 2020 | 3 | 2020 |
| Monogenic diabetes in Slovakia: mutational spectrum and HNF1A functional studies D Gasperikova, M Skopkova, T Valkovicova, Z Dobiasova, M Sklenar, ... DIABETOLOGIA 65 (SUPPL 1), S158-S158, 2022 | | 2022 |
| Functional analysis of novel HNF1A variants found in MODY patients in Slovakia T Valkovicova, Z Dobiasova, J Stanik, M Skopkova, D Gasperikova EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 208-208, 2022 | | 2022 |
| Comparison of diabetes phenotype in children and their mothers with permanent neonatal diabetes mellitus carrying the same variants J Stanik, L Barak, A Dankovcikova, T Valkovicova, M Skopkova, ... Endocrine Regulations 54 (4), 260-265, 0 | | |
