Novel insights into genetics and clinics of the HNF1A-MODY

por Valkovicova Terezia, Skopkova Martina, Stanik Juraj, Gasperikova Daniela
Publicado 2019

Comparison of diabetes phenotype in children and their mothers with permanent neonatal diabetes mellitus carrying the same KCNJ11 variants

por Stanik Juraj, Barak Lubomir, Dankovcikova Adriana, Valkovicova Terezia, Skopkova Martina, Gasperikova Daniela
Publicado 2020

Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients

por Danis Daniel, Brennerova Katarina, Skopkova Martina, Kurdiova Timea, Ukropec Jozef, Stanik Juraj, Kolnikova Miriam, Gasperikova Daniela
Publicado 2018