Telomere Attrition in Chronic Kidney Diseases

por Levstek, Tina, Trebušak Podkrajšek, Katarina
Publicado 2023

Special Issue “Genetics and Epigenetics in Endocrine Disorders”

por Trebušak Podkrajšek, Katarina, Kotnik, Primož
Publicado 2023

Biomarkers of Fabry Nephropathy: Review and Future Perspective

por Levstek, Tina, Vujkovac, Bojan, Trebusak Podkrajsek, Katarina
Publicado 2020

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

por Kovač, Jernej, Klančar, Gašper, Trebušak Podkrajšek, Katarina, Battelino, Saba
Publicado 2017

Telomere Attrition in Neurodegenerative Disorders

por Levstek, Tina, Kozjek, Eva, Dolžan, Vita, Trebušak Podkrajšek, Katarina
Publicado 2020

Urinary-derived extracellular vesicles reveal a distinct microRNA signature associated with the development and progression of Fabry nephropathy

por Levstek, Tina, Vujkovac, Bojan, Cokan Vujkovac, Andreja, Trebušak Podkrajšek, Katarina
Publicado 2023

The Importance of Early Genetic Diagnostics of Hearing Loss in Children

por Božanić Urbančič, Nina, Battelino, Saba, Tesovnik, Tine, Trebušak Podkrajšek, Katarina
Publicado 2020

Novel GRHL2 Gene Variant Associated with Hearing Loss: A Case Report and Review of the Literature

por Trebusak Podkrajsek, Katarina, Tesovnik, Tine, Bozanic Urbancic, Nina, Battelino, Saba
Publicado 2021

LPA 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) Levels

por Rehberger Likozar, Andreja, Blinc, Aleš, Trebušak Podkrajšek, Katarina, Šebeštjen, Miran
Publicado 2021

An Intron c.103-3T>C Variant of the AMELX Gene Causes Combined Hypomineralized and Hypoplastic Type of Amelogenesis Imperfecta: Case Series and Review of the Literature

por Leban, Tina, Trebušak Podkrajšek, Katarina, Kovač, Jernej, Fidler, Aleš, Pavlič, Alenka
Publicado 2022

Interplay between microRNAs, Serum Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9), and Lipid Parameters in Patients with Very High Lipoprotein(a) Treated with PCSK9 Inhibito...

por Levstek, Tina, Karun, Tina, Rehberger Likozar, Andreja, Šebeštjen, Miran, Trebušak Podkrajšek, Katarina
Publicado 2023

Clinical, Genetic and Immunological Characteristics of Paediatric Autoimmune Polyglandular Syndrome Type 1 Patients in Slovenia

por BRATANIC, Nina, KISAND, Kai, AVBELJ STEFANIJA, Magdalena, BATTELINO, Tadej, TREBUSAK PODKRAJSEK, Katarina
Publicado 2015

The Influence of Treatment with PCSK9 Inhibitors and Variants in the CRP (rs1800947), TNFA (rs1800629), and IL6 (rs1800795) Genes on the Corresponding Inflammatory Markers in Patie...

por Levstek, Tina, Podkrajšek, Nik, Rehberger Likozar, Andreja, Šebeštjen, Miran, Trebušak Podkrajšek, Katarina
Publicado 2022

Association of Average Telomere Length with Body-Mass Index and Vitamin D Status in Juvenile Population with Type 1 Diabetes

por TESOVNIK, Tine, KOVAC, Jernej, HOVNIK, Tinka, KOTNIK, Primoz, BATTELINO, Tadej, TREBUSAK PODKRAJSEK, Katarina
Publicado 2015

Cytogenetic and Molecular Genetic Characterization of Children with Short Stature

por HOVNIK, Tinka, ŠMIGOC SCHWEIGER, Darja, KOTNIK, Primož, KOVAČ, Jernej, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina
Publicado 2015

GNRHR-related central hypogonadism with spontaneous recovery – case report

por Šmigoc Schweiger, Darja, Davidović Povše, Maja, Trebušak Podkrajšek, Katarina, Battelino, Tadej, Avbelj Stefanija, Magdalena
Publicado 2022

Detection of Del/Dup Inside SHOX/PAR1 Region in Children and Young Adults with Idiopathic Short Stature

por Stritar, Jera, Stavber, Lana, Ficko, Maja, Kotnik, Primož, Battelino, Tadej, Trebušak Podkrajšek, Katarina, Hovnik, Tinka
Publicado 2021

Multifocal gastric adenocarcinoma in a patient with LRBA deficiency

por Bratanič, Nina, Kovač, Jernej, Pohar, Katka, Trebušak Podkrajšek, Katarina, Ihan, Alojz, Battelino, Tadej, Avbelj Stefanija, Magdalena
Publicado 2017

Urinary Extracellular Vesicles and Their miRNA Cargo in Patients with Fabry Nephropathy

por Levstek, Tina, Mlinšek, Teo, Holcar, Marija, Goričar, Katja, Lenassi, Metka, Dolžan, Vita, Vujkovac, Bojan, Trebušak Podkrajšek, Katarina
Publicado 2021

Childhood Osteoporosis and Presentation of Two Cases with Osteogenesis Imperfecta Type V

por BRATANIC, Nina, DZODAN, Bojana, TREBUSAK PODKRAJSEK, Katarina, BERTOK, Sara, OSTANEK, Barbara, MARC, Janja, BATTELINO, Tadej, AVBELJ STEFANIJA, Magdalena
Publicado 2015