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Pediatric Endocrinology, Diabetes, and Metabolism|November 8, 2021
Mucopolysaccharidosis III: Molecular basis and treatmentLidvana Spahiu, Emir Behluli, Borut Peterlin, et al.
Frontiers in Neurology|July 11, 2026
How we diagnose and treat hereditary transthyretin-mediated amyloidosis with polyneuropathy in the Balkan region: an expert opinionIvailo Tournev, Janez Zidar, Borut Peterlin, et al.
Pflugers Archiv : European Journal of Physiology|February 9, 2017
DD Genotype of the angiotensin - converting enzyme gene and stroke in Slovenian populationBorut Peterlin, Tomaž Milanez, Jan Kobal, et al.
Fertility and Sterility|February 16, 2013
Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature reviewNina Pereza, Ksenija Črnjar, Alena Buretić-Tomljanović, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|November 5, 2003
Factor V Leiden, prothrombin 20210G --> A, methylenetetrahydrofolate reductase 677C --> T and plasminogen activator inhibitor 4G/5G polymorphism in women with pregnancy-related venous thromboembolismLeon Meglic, Mojca Stegnar, Tomaz Milanez, et al.
Molecular Vision|August 7, 2008
Local and genetic determinants of vascular endothelial growth factor expression in advanced proliferative diabetic retinopathyMojca Globocnik Petrovic, Peter Korosec, Mitja Kosnik, et al.
International Journal of Molecular Sciences|October 26, 2024
Protective Effect of <i>EBF Transcription Factor 1</i> (<i>EBF1</i>) Polymorphism in Sporadic and Familial Spontaneous Preterm Birth: Insights from a Case-Control StudyTea Mladenić, Jasenka Wagner, Mirta Kadivnik, et al.
Genes|December 23, 2023
Evaluation of Optical Genome Mapping in Clinical Genetic Testing of Facioscapulohumeral Muscular DystrophyAnja Kovanda, Luca Lovrečić, Gorazd Rudolf, et al.
Scientific Reports|June 26, 2019
Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genesLovro Vidmar, Ales Maver, Jelena Drulović, et al.
Genes|September 27, 2025
Novel <i>ATP7A</i> Splice-Site Variant Causing Distal Motor Neuropathy and Occipital Horn Syndrome: Two Siblings and Literature ReviewKarin Writzl, Maruša Škrjanec Pušenjak, Matevž Jus, et al.
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