Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients
Danis, Daniel, Brennerova, Katarina, Skopkova, Martina, Kurdiova, Timea, Ukropec, Jozef, Stanik, Juraj, Kolnikova, Miriam, Gasperikova, Daniela
Novel insights into genetics and clinics of the HNF1A-MODY
Valkovicova, Terezia, Skopkova, Martina, Stanik, Juraj, Gasperikova, Daniela
Comparison of diabetes phenotype in children and their mothers with permanent neonatal diabetes mellitus carrying the same KCNJ11 variants
Stanik, Juraj, Barak, Lubomir, Dankovcikova, Adriana, Valkovicova, Terezia, Skopkova, Martina, Gasperikova, Daniela