Genetic Polymorphisms in Genes Encoding Antioxidant Enzymes Are Associated With Diabetic Retinopathy in Type 1 Diabetes

por Hovnik, Tinka, Dolžan, Vita, Bratina, Nataša Uršič, Podkrajšek, Katarina Trebušak, Battelino, Tadej
Publicado 2009

Changes in The Use of Alcohol and Tobacco in Slovenia During the First Wave of The SARS-COV-2 Pandemic

por Krnel, Sandra Radoš, Kilian, Carolin, Keršmanc, Marjetka Hovnik, Roškar, Maja, Koprivnikar, Helena
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

Characterization of a de novo sSMC 17 detected in a girl with developmental delay and dysmorphic features

por Stavber, Lana, Bertok, Sara, Kovač, Jernej, Volk, Marija, Lovrečić, Luca, Battelino, Tadej, Hovnik, Tinka
Publicado 2017

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

Changes in Alcohol Consumption among Different Population Groups during the SARS-CoV-2 Pandemic: Outcomes of the Slovenian Cross-Sectional National Survey (SI-PANDA)

por Radoš Krnel, Sandra, Roškar, Maja, Hovnik Keršmanc, Marjetka, Rehberger, Maruša, Levičnik, Gorazd, Hočevar Grom, Ada
Publicado 2022

A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6, GRHL3, and TBX22

por Slavec, Lara, Geršak, Ksenija, Eberlinc, Andreja, Hovnik, Tinka, Lovrečić, Luca, Mlinarič-Raščan, Irena, Karas Kuželički, Nataša
Publicado 2023

An Adolescent Boy with Klinefelter Syndrome and 47,XXY/46,XX Mosaicism: Case Report and Review of Literature

por Hovnik, Tinka, Zitnik, Eva, Avbelj Stefanija, Magdalena, Bertok, Sara, Sedej, Katarina, Bancic Silva, Vesna, Battelino, Tadej, Groselj, Urh
Publicado 2022

High frequency of pathogenic ACAN variants including an intragenic deletion in selected individuals with short stature

por Stavber, L, Hovnik, T, Kotnik, P, Lovrečić, L, Kovač, J, Tesovnik, T, Bertok, S, Dovč, K, Debeljak, M, Battelino, T, Avbelj Stefanija, M
Publicado 2019

Dual Role of PTPN22 but Not NLRP3 Inflammasome Polymorphisms in Type 1 Diabetes and Celiac Disease in Children

por Smigoc Schweiger, Darja, Goricar, Katja, Hovnik, Tinka, Mendez, Andrijana, Bratina, Natasa, Brecelj, Jernej, Vidan-Jeras, Blanka, Battelino, Tadej, Dolzan, Vita
Publicado 2019

Clinical and Molecular Cytogenetic Characterisation of Children with Developmental Delay and Dysmorphic Features

por BERTOK, Sara, ŽERJAV TANŠEK, Mojca, KOTNIK, Primož, BATTELINO, Tadej, VOLK, Marija, PECILE, Vanna, CLEVA, Lisa, GASPARINI, Paolo, KOVAČ, Jernej, HOVNIK, Tinka
Publicado 2015

Early Discovery of Children With Lysosomal Acid Lipase Deficiency With the Universal Familial Hypercholesterolemia Screening Program

por Sustar, Ursa, Groselj, Urh, Trebusak Podkrajsek, Katarina, Mlinaric, Matej, Kovac, Jernej, Thaler, Martin, Drole Torkar, Ana, Skarlovnik, Ajda, Battelino, Tadej, Hovnik, Tinka
Publicado 2022

Heterozygous NPR2 Variants in Idiopathic Short Stature

por Stavber, Lana, Gaia, Maria Joao, Hovnik, Tinka, Jenko Bizjan, Barbara, Debeljak, Maruša, Kovač, Jernej, Omladič, Jasna Šuput, Battelino, Tadej, Kotnik, Primož, Dovč, Klemen
Publicado 2022