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Atherosclerosis|October 2, 2018
Universal screening for familial hypercholesterolemia in children: The Slovenian model and literature reviewUrh Groselj, Jernej Kovac, Ursa Sustar, et al.
Frontiers in Genetics|September 2, 2022
A homozygous variant in the GPIHBP1 gene in a child with severe hypertriglyceridemia and a systematic literature reviewUrsa Sustar, Urh Groselj, Sabeen Abid Khan, et al.
Frontiers in Genetics|July 29, 2022
Early Discovery of Children With Lysosomal Acid Lipase Deficiency With the Universal Familial Hypercholesterolemia Screening ProgramUrsa Sustar, Urh Groselj, Katarina Trebusak Podkrajsek, et al.
Atherosclerosis|February 4, 2025
Cascade screening of a Pakistani consanguineous familial hypercholesterolemia cohort: Identification of seven new homozygous patientsQuratul Ain, Jaka Sikonja, Fouzia Sadiq, et al.
Atherosclerosis|November 26, 2024
Prevalence, genetic variants, and clinical implications of hypocholesterolemia in childrenUrh Groselj, Jan Kafol, Neza Molk, et al.
Frontiers in Medicine|June 29, 2023
Non-alcoholic fatty liver disease in a pediatric patient with heterozygous familial hypobetalipoproteinemia due to a novel APOB variant: a case report and systematic literature reviewNeza Molk, Mojca Bitenc, Darja Urlep, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 1, 2022
Universal screening for familial hypercholesterolemia in 2 populationsUrsa Sustar, Olga Kordonouri, Matej Mlinaric, et al.
Frontiers in Genetics|October 23, 2020
Genetic and Clinical Characteristics of Patients With Homozygous and Compound Heterozygous Familial Hypercholesterolemia From Three Different Populations: Case SeriesTatiana Marusic, Ursa Sustar, Fouzia Sadiq, et al.
Frontiers in Endocrinology|June 24, 2024
Genetic and clinical characteristics of patients with lipoprotein lipase deficiency from Slovenia and Pakistan: case series and systematic literature reviewQuratul Ain, Matija Cevc, Tatiana Marusic, et al.
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