Telomere Attrition in Neurodegenerative Disorders by Tina Levstek, Eva Kozjek, Vita Dolžan, Katarina Trebušak Podkrajšek, Katarina Trebušak Podkrajšek

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Telomere Attrition in Chronic Kidney Diseases by Tina Levstek, Katarina Trebušak Podkrajšek

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Discovering the Unexpected with the Utilization of NGS in Diagnostics of Non-syndromic Hearing Loss Disorders: The Family Case of ILDR1-Dependent Hearing Loss Disorder by Jernej Kovač, Gašper Klančar, Katarina Trebušak Podkrajšek, Katarina Trebušak Podkrajšek, Saba Battelino, Saba Battelino

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Urinary-derived extracellular vesicles reveal a distinct microRNA signature associated with the development and progression of Fabry nephropathy by Tina Levstek, Tina Levstek, Bojan Vujkovac, Andreja Cokan Vujkovac, Katarina Trebušak Podkrajšek, Katarina Trebušak Podkrajšek

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HUMANE GENETSKE SPREMEMBE IN NJIHOVO DOLOČANJE: TRENUTNO STANJE IN OBETI ZA PRIHODNOST by Lara Slavec, Ksenija Geršak, Nataša Karas Kuželički, Katarina Trebušak Podkrajšek

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Genetic and clinical characteristics of patients with phenylketonuria in Slovenia by Urh Grošelj, Mojca Žerjav Tanšek, Katarina Trebušak Podkrajšek, Tadej Battelino

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<i>LPA</i> Genotypes and Haplotypes Are Associated with Lipoprotein(a) Levels but Not Arterial Wall Properties in Stable Post-Coronary Event Patients with Very High Lipoprotein(a)... by Andreja Rehberger Likozar, Aleš Blinc, Katarina Trebušak Podkrajšek, Miran Šebeštjen

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The Importance of Early Genetic Diagnostics of Hearing Loss in Children by Nina Božanić Urbančič, Saba Battelino, Tine Tesovnik, Katarina Trebušak Podkrajšek

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Assessment of the Telomere Length and Its Effect on the Symptomatology of Parkinson’s Disease by Tina Levstek, Sara Redenšek, Maja Trošt, Vita Dolžan, Katarina Trebušak Podkrajšek

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Dynamics of Leukocyte Telomere Length in Patients with Fabry Disease by Tina Levstek, Nika Breznik, Bojan Vujkovac, Albina Nowak, Katarina Trebušak Podkrajšek

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The Influence of Treatment with PCSK9 Inhibitors and Variants in the <i>CRP</i> (rs1800947), <i>TNFA</i> (rs1800629), and <i>IL6</i> (rs1800795) Genes on the Corresponding Inflamma... by Tina Levstek, Nik Podkrajšek, Andreja Rehberger Likozar, Miran Šebeštjen, Katarina Trebušak Podkrajšek

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Clinical role of CYP2C19 polymorphisms in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency by Urh Grošelj, Mojca Žerjav Tanšek, Katarina Trebušak Podkrajšek, Tinka Hovnik, Tadej Battelino, Vita Dolžan

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GNRHR-related central hypogonadism with spontaneous recovery – case report by Darja Šmigoc Schweiger, Maja Davidović Povše, Katarina Trebušak Podkrajšek, Tadej Battelino, Magdalena Avbelj Stefanija

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Treatment with PCSK9 inhibitors influences microRNAs expression and changes of arterial wall properties: a randomized controlled trial by Andreja Rehberger Likozar, Tina Levstek, Tina Karun, Katarina Trebušak Podkrajšek, Janja Zupan, Miran Šebeštjen

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

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Multifocal gastric adenocarcinoma in a patient with LRBA deficiency by Nina Bratanič, Jernej Kovač, Katka Pohar, Katarina Trebušak Podkrajšek, Alojz Ihan, Tadej Battelino, Magdalena Avbelj Stefanija

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SPTB related spherocytosis in a three-generation family presenting with kidney failure in adulthood due to co-occurrence of UMOD disease causing variant by Anamarija Meglic, Marusa Debeljak, Jernej Kovac, Alenka Trampus Bakija, Vladan Rajic, Nika Kojc, Katarina Trebusak Podkrajsek

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DENTAL ENAMEL HYPOPLASIA AS A PRESENTING SIGN OF AUTOIMMUNE POLYENDOCRINOPATHY WITH CANDIDIASIS-ECTODERMAL DYSTROPHY - A CASE REPORT by Lea Regoršek Vrabec, Tina Leban, Katarina Trebušak Podkrajšek, Nataša Bratina, Sara Bertok, Alenka Pavlič, Magdalena Avbelj Stefanija

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

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Case Report: Multiple prolactinomas in a young man with Kallmann syndrome and familial hypocalciuric hypercalcemia by Mojca Jensterle, Mojca Jensterle, Andrej Janež, Andrej Janež, Tina Vipotnik Vesnaver, Maruša Debeljak, Maruša Debeljak, Nika Breznik, Katarina Trebušak Podkrajšek, Katarina Trebušak Podkrajšek, Rok Herman, Rok Herman, Eric Fliers, Tadej Battelino, Tadej Battelino, Magdalena Avbelj Stefanija, Magdalena Avbelj Stefanija

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