Biochemická a molekulárno-genetická diagnostika porúch β-oxidácie karboxylových kyselín v SR |
2014 |
Cellular metabolism, physiology, molecular biology and genetics |
Androgen receptor and its mutations |
2014 |
Cellular metabolism, physiology, molecular biology and genetics |
Rutledge lethal multiple congenital anomaly syndrome: a rare form of Smith-Lemli-Opitz syndrome |
2017 |
Cellular metabolism, physiology, molecular biology and genetics (clinical trials) |
Vrodená fibrinogenémia a dysfibrinogenémia |
2020 |
Cellular metabolism, physiology, molecular biology and genetics (clinical trials) |
CADASIL syndróm – najčastejšia hereditárna príčina ischemických mozgových príhod |
2021 |
Molecular biology and genetics |
Úvod do farmakogenetiky |
2021 |
Molecular biology and genetics |
Cerebrotendinózna xantomatóza, kazuistika adultného pacienta |
2021 |
Molecular biology and genetics |