Ethics of Vaccination in Childhood—A Framework Based on the Four Principles of Biomedical Ethics

by Rus, Meta, Groselj, Urh
Published in Vaccines (Basel) (2021)

Development of a pilot rare disease registry: a focus group study of initial steps towards the establishment of a rare disease ecosystem in Slovenia

by Stanimirovic, Dalibor, Murko, Eva, Battelino, Tadej, Groselj, Urh
Published in Orphanet J Rare Dis (2019)

High-Sensitivity C-Reactive Protein and Carotid Intima Media Thickness as Markers of Subclinical Inflammation and Atherosclerosis in Pediatric Patients with Hypercholesterolemia

by Blinc, Lana, Mlinaric, Matej, Battelino, Tadej, Groselj, Urh
Published in Molecules (2020)

Experiences of Slovene ICU Physicians with End-of-Life Decision Making: A Nation-Wide Survey

by Groselj, Urh, Orazem, Miha, Kanic, Maja, Vidmar, Gaj, Grosek, Stefan
Published 2014

Carotid Intima-Media Thickness in Healthy Children and Adolescents: Normative Data and Systematic Literature Review

by Drole Torkar, Ana, Plesnik, Emil, Groselj, Urh, Battelino, Tadej, Kotnik, Primoz
Published in Front Cardiovasc Med (2020)

Drafting a blueprint for the design of a rare disease ecosystem in Slovenia: Identifying salient opportunities and outlining policy recommendations

by Stanimirovic, Dalibor, Murko, Eva, Battelino, Tadej, Groselj, Urh, Zerjav Tansek, Mojca
Published in J Glob Health (2021)

A patient with glycogen storage disease type 0 and a novel sequence variant in GYS2: a case report and literature review

by Arko, Janez Jan, Debeljak, Marusa, Tansek, Mojca Zerjav, Battelino, Tadej, Groselj, Urh
Published in J Int Med Res (2020)

Case Report: Liver Transplantation in Homozygous Familial Hypercholesterolemia (HoFH)—Long-Term Follow-Up of a Patient and Literature Review

by Mlinaric, Matej, Bratanic, Nevenka, Dragos, Vlasta, Skarlovnik, Ajda, Cevc, Matija, Battelino, Tadej, Groselj, Urh
Published in Front Pediatr (2020)

Normalization of obstructive cardiomyopathy and improvement of hepatopathy on ketogenic diet in patient with glycogen storage disease (GSD) type IIIa

by Marusic, Tatiana, Zerjav Tansek, Mojca, Sirca Campa, Andreja, Mezek, Ajda, Berden, Pavel, Battelino, Tadej, Groselj, Urh
Published in Mol Genet Metab Rep (2020)

Anthropometry and bone mineral density in treated and untreated hyperphenylalaninemia

by Zerjav Tansek, Mojca, Bertoncel, Ana, Sebez, Brina, Zibert, Janez, Groselj, Urh, Battelino, Tadej, Avbelj Stefanija, Magdalena
Published in Endocr Connect (2020)

Data highlighting effects of Ketogenic diet on cardiomyopathy and hepatopathy in Glycogen storage disease Type IIIA

by Marusic, Tatiana, Zerjav Tansek, Mojca, Sirca Campa, Andreja, Mezek, Ajda, Berden, Pavel, Battelino, Tadej, Groselj, Urh
Published in Data Brief (2020)

The first nationwide study on facing and solving ethical dilemmas among healthcare professionals in Slovenia

by Grosek, Štefan, Kučan, Rok, Grošelj, Jon, Oražem, Miha, Grošelj, Urh, Erčulj, Vanja, Lajovic, Jaro, Borovečki, Ana, Ivanc, Blaž
Published in PLoS One (2020)

Hypercholesterolemia in Two Siblings with Resistance to Thyroid Hormones Due to Disease-Causing Variant in Thyroid Hormone Receptor (THRB) Gene

by Pajek, Maja, Avbelj Stefanija, Magdalena, Trebusak Podkrajsek, Katarina, Suput Omladic, Jasna, Zerjav Tansek, Mojca, Battelino, Tadej, Groselj, Urh
Published in Medicina (Kaunas) (2020)

Next-Generation Sequencing in Newborn Screening: A Review of Current State

by Remec, Ziga I., Trebusak Podkrajsek, Katarina, Repic Lampret, Barbka, Kovac, Jernej, Groselj, Urh, Tesovnik, Tine, Battelino, Tadej, Debeljak, Marusa
Published in Front Genet (2021)

Precocious puberty in a girl with 3-methylglutaconic aciduria type 1 (3-MGA-I) due to a novel AUH gene mutation

by Bizjak, Neli, Zerjav Tansek, Mojca, Avbelj Stefanija, Magdalena, Repic Lampret, Barbka, Mezek, Ajda, Drole Torkar, Ana, Battelino, Tadej, Groselj, Urh
Published in Mol Genet Metab Rep (2020)

Central TSH Dysregulation in a Patient with Familial Non-Autoimmune Autosomal Dominant Hyperthyroidism Due to a Novel Thyroid-Stimulating Hormone Receptor Disease-Causing Variant

by Suput Omladic, Jasna, Pajek, Maja, Groselj, Urh, Trebusak Podkrajsek, Katarina, Avbelj Stefanija, Magdalena, Zerjav Tansek, Mojca, Kotnik, Primoz, Battelino, Tadej, Smigoc Schweiger, Darja
Published in Medicina (Kaunas) (2021)

Two Cases With an Early Presented Proopiomelanocortin Deficiency—A Long-Term Follow-Up and Systematic Literature Review

by Gregoric, Nadan, Groselj, Urh, Bratina, Natasa, Debeljak, Marusa, Zerjav Tansek, Mojca, Suput Omladic, Jasna, Kovac, Jernej, Battelino, Tadej, Kotnik, Primoz, Avbelj Stefanija, Magdalena
Published in Front Endocrinol (Lausanne) (2021)

Newborn Screening in Slovenia

by ŠMON, Andraž, GROŠELJ, Urh, ŽERJAV TANŠEK, Mojca, BIČEK, Ajda, OBLAK, Adrijana, ZUPANČIČ, Mirjana, KRŽIŠNIK, Ciril, REPIČ LAMPR ET, Barbka, MURKO, Simona, HOJKER, Sergej, BATTELINO, Tadej
Published in Zdr Varst (2015)

Genetic and Clinical Characteristics of Patients With Homozygous and Compound Heterozygous Familial Hypercholesterolemia From Three Different Populations: Case Series

by Marusic, Tatiana, Sustar, Ursa, Sadiq, Fouzia, Kotori, Vjosa, Mlinaric, Matej, Kovac, Jernej, Shafi, Saeed, Khan, Iqbal, Cevc, Matija, Trebusak Podkrajsek, Katarina, Battelino, Tadej, Groselj, Urh
Published in Front Genet (2020)

Therapy-type related long-term outcomes in mucopolysaccaridosis type II (Hunter syndrome) – Case series

by Zerjav Tansek, Mojca, Kodric, Jana, Klemencic, Simona, Boelens, Jaap Jan, van Hasselt, Peter M., Drole Torkar, Ana, Doric, Maja, Koren, Alenka, Avcin, Simona, Battelino, Tadej, Groselj, Urh
Published in Mol Genet Metab Rep (2021)