Universal screening for familial hypercholesterolemia in children: The Slovenian model and literature review von Groselj, Urh, Kovac, Jernej, Sustar, Ursa, Mlinaric, Matej, Fras, Zlatko, Podkrajsek, Katarina Trebusak, Battelino, Tadej

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A homozygous variant in the GPIHBP1 gene in a child with severe hypertriglyceridemia and a systematic literature review von Sustar, Ursa, Groselj, Urh, Khan, Sabeen Abid, Shafi, Saeed, Khan, Iqbal, Kovac, Jernej, Bizjan, Barbara Jenko, Battelino, Tadej, Sadiq, Fouzia

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Early Discovery of Children With Lysosomal Acid Lipase Deficiency With the Universal Familial Hypercholesterolemia Screening Program von Sustar, Ursa, Groselj, Urh, Trebusak Podkrajsek, Katarina, Mlinaric, Matej, Kovac, Jernej, Thaler, Martin, Drole Torkar, Ana, Skarlovnik, Ajda, Battelino, Tadej, Hovnik, Tinka

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Genetic and clinical characteristics of patients with lipoprotein lipase deficiency from Slovenia and Pakistan: case series and systematic literature review von Ain, Quratul, Cevc, Matija, Marusic, Tatiana, Sikonja, Jaka, Sadiq, Fouzia, Sustar, Ursa, Mlinaric, Matej, Kovac, Jernej, Batool, Hijab, Khan, Mohammad Iqbal, Trebusak Podkrajsek, Katarina, Bizjan, Barbara Jenko, Battelino, Tadej, Fras, Zlatko, Ajmal, Muhammad, Groselj, Urh

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Genetic and Clinical Characteristics of Patients With Homozygous and Compound Heterozygous Familial Hypercholesterolemia From Three Different Populations: Case Series von Marusic, Tatiana, Sustar, Ursa, Sadiq, Fouzia, Kotori, Vjosa, Mlinaric, Matej, Kovac, Jernej, Shafi, Saeed, Khan, Iqbal, Cevc, Matija, Podkrajsek, Katarina Trebusak, Battelino, Tadej, Groselj, Urh

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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 rev... von Molk, Neza, Bitenc, Mojca, Urlep, Darja, Zerjav Tansek, Mojca, Bertok, Sara, Trebusak Podkrajsek, Katarina, Sustar, Ursa, Kovac, Jernej, Battelino, Tadej, Debeljak, Marusa, Groselj, Urh

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Additional cardiovascular disease risk factors present in children with familial hypercholesterolemia at the first visit von Mlinaric, Matej, Sustar, Ursa, Sikonja, Jaka, Kovač, Jernej, Groselj, Urh, Battelino, Tadej

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Genetic background of hypercholesterolemia in a large cohort of pediatric patients detected through universal screening program von Sustar, Ursa, Mlinaric, Matej, Kovač, Jernej, Podkrajšek, Katarina Trebušak, Battelino, Tadej, Groselj, Urh

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Genetic screening of familial hypercholesterolemia cohort from Pakistan von Sadiq, Fouzia, Groselj, Urh, Ain, Quratul, Khan, Madeeha, Sikonja, Jaka, Sustar, Ursa, Gorjanc, Tevz, Shafi, Muhammad, Khan, Mohammad

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Prevalence, genetic variants, and clinical implications of hypocholesterolemia in children von Groselj, Urh, Kafol, Jan, Molk, Neza, Sedej, Katarina, Mlinaric, Matej, Sikonja, Jaka, Sustar, Ursa, Kern, Barbara Cugalj, Kovac, Jernej, Battelino, Tadej, Debeljak, Marusa

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Universal screening for familial hypercholesterolemia in 2 populations von Sustar, Ursa, Kordonouri, Olga, Mlinaric, Matej, Kovac, Jernej, Arens, Stefan, Sedej, Katarina, Jenko Bizjan, Barbara, Trebusak Podkrajsek, Katarina, Danne, Thomas, Battelino, Tadej, Groselj, Urh

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Evaluation of Body Mass Index, Overweight and Obesity Status, and Cholesterol Levels in Younger Children von Sustar, Ursa, Kordonouri, Olga, Arens, Stefan, Kovac, Jernej, Sedej, Katarina, Battelino, Tadej, Groselj, Urh

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Universal Screening for Familial Hypercholesterolemia in Two Populations von Sustar, Ursa, Mlinaric, Matej, Kovac, Jernej, Arens, Stefan, Bizjan, Barbara Jenko, Podkrajsek, Katarina Trebusak, Danne, Thomas, Battelino, Tadej, Kordonouri, Olga, Groselj, Urh

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Tst gene mediates protection against palmitate-induced inflammation in 3T3-L1 adipocytes von Lainšček, Duško, Šuštar, Urša, Carter, Roderick N., Morton, Nicholas M., Horvat, Simon

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Clinical characteristics of children with lysosomal acid lipase deficiency von Ursa Sustar

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Clinical characteristics of children with lysosomal acid lipase deficiency von Ursa Sustar

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Clinical characteristics of a pediatric patient with heterozygous familial hypobetalipoproteinemia due to a novel APOB variant von Neza Molk

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Clinical characteristics of a pediatric patient with heterozygous familial hypobetalipoproteinemia due to a novel APOB variant von Neza Molk

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Textual analysis of corporate sustainability reporting and corporate ESG scores von Ferjančič, Urša, Ichev, Riste, Lončarski, Igor, Montariol, Syrielle, Pelicon, Andraž, Pollak, Senja, Sitar Šuštar, Katarina, Toman, Aleš, Valentinčič, Aljoša, Žnidaršič, Martin

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KULTURA NASELBINSKEGA PROSTORA V SLOVENIE/THE CULTURE OF SETTLEMENT AREAS IN SLOVENIA von Fikfak, Alenka, Dinevski, Milan, Jezek, Petra, Nagode, Nace, Rogic, Gasper Skalar, Vovko, Ursa Suhadolnik, Sustar, Jakob

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