M. Repiský

Peroxisomal D-bifunctional protein deficiency: First case reports from Slovakia.

S. Šutovský, R. Petrovic, J. Chandoga, 2015, Gene.

An unusually high frequency of SCAD deficiency caused by two pathogenic variants in the ACADS gene and its relationship to the ethnic structure in Slovakia

D. Behúlová, P. Jungová, J. Chandoga, 2018, BMC Medical Genetics.

Serum butyrylcholinesterase/HDL-cholesterol ratio and atherogenic index of plasma in patients with fatty liver disease.

V. Kupčová, M. Repiský, L. Turecký, 2021, Vnitrni lekarstvi.

Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism

J. Chandoga, J. Konkoľová, M. Repiský, 2017, BMC Medical Genetics.