C. Šebová

Lipid levels and their genetic regulation in patients with familial hypercholesterolemia and familial defective apolipoprotein B-100: the MEDPED Slovakia Project.

L. Iacoviello, K. Rašlová, M. Donati, 2003, Atherosclerosis. Supplements.

Congenital disorders of glycosylation - an umbrella term for rapidly expanding group of rare genetic metabolic disorders - importance of physical investigation.

P. Baráth, B. Siváková, M. Nemčovič, 2021, Bratislavske lekarske listy.

Conjugated hyperbilirubinaemia as the first manifestation of mevalonic aciduria in a term newborn.

D. Behúlová, C. Šebová, E. Ujhazy, 2009, Neuro endocrinology letters.

A novel homozygous mutation in the human ALG12 gene results in an aberrant profile of oligomannose N‐glycans in patient's serum

A. Hlavatá, P. Baráth, B. Siváková, 2021, American journal of medical genetics. Part A.

ACY1 deficiency: long time monitoring of N-acetylated amino acids concentrations in urine of ACY1 deficient siblings by NMR

C. Šebová, M. Matulová, I. Uhliariková, 2022, Chemical Papers.

Inherited metabolic disorders of glycoconjugate metabolism.

P. Baráth, M. Nemčovič, Z. Pakanová, 2020, Bratislavske lekarske listy.