Hovnik T - Search Results

1

Clinical Role of CYP2C19 Polymorphisms in Patients with Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency.

Grošelj U, Žerjav Tanšek M, Trebušak Podkrajšek K, Hovnik T, Battelino T, Vita D. Grošelj U, et al. Among authors: hovnik t. Acta Chim Slov. 2016;63(1):33-7. doi: 10.17344/acsi.2015.1797. Acta Chim Slov. 2016. PMID: 26970786

2

Genetic Variability in Slovenian Cohort of Patients with Oculocutaneous Albinism.

Hovnik T, Debeljak M, Tekavčič Pompe M, Bertok S, Battelino T, Stirn Kranjc B, Trebušak Podkrajšek K. Hovnik T, et al. Acta Chim Slov. 2021 Sep;68(3):683-692. Acta Chim Slov. 2021. PMID: 34897530

3

Five novel mutations and two large deletions in a population analysis of the phenylalanine hydroxylase gene.

Groselj U, Tansek MZ, Kovac J, Hovnik T, Podkrajsek KT, Battelino T. Groselj U, et al. Among authors: hovnik t. Mol Genet Metab. 2012 Jun;106(2):142-8. doi: 10.1016/j.ymgme.2012.03.015. Epub 2012 Apr 1. Mol Genet Metab. 2012. PMID: 22513348

4

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

Sustar U, Groselj U, Trebusak Podkrajsek K, Mlinaric M, Kovac J, Thaler M, Drole Torkar A, Skarlovnik A, Battelino T, Hovnik T. Sustar U, et al. Among authors: hovnik t. Front Genet. 2022 Jul 12;13:936121. doi: 10.3389/fgene.2022.936121. eCollection 2022. Front Genet. 2022. PMID: 35903350 Free PMC article.

5

GPR143 gene mutation analysis in pediatric patients with albinism.

Trebušak Podkrajšek K, Stirn Kranjc B, Hovnik T, Kovač J, Battelino T. Trebušak Podkrajšek K, et al. Among authors: hovnik t. Ophthalmic Genet. 2012 Sep;33(3):167-70. doi: 10.3109/13816810.2011.559651. Epub 2012 Apr 9. Ophthalmic Genet. 2012. PMID: 22486324

6

Metabolic control, ApoE genotypes, and dyslipidemia in children, adolescents and young adults with type 1 diabetes.

Macedoni M, Hovnik T, Plesnik E, Kotnik P, Bratina N, Battelino T, Groselj U. Macedoni M, et al. Among authors: hovnik t. Atherosclerosis. 2018 Jun;273:53-58. doi: 10.1016/j.atherosclerosis.2018.04.013. Epub 2018 Apr 12. Atherosclerosis. 2018. PMID: 29679801

7

Cytogenetic and Molecular Genetic Characterization of Children with Short Stature.

Hovnik T, Šmigoc Schweiger D, Kotnik P, Kovač J, Battelino T, Trebušak Podkrajšek K. Hovnik T, et al. Zdr Varst. 2015 Mar 13;54(2):98-102. doi: 10.1515/sjph-2015-0015. eCollection 2015 Jun. Zdr Varst. 2015. PMID: 27646915 Free PMC article.

8

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

Tesovnik T, Kovac J, Hovnik T, Kotnik P, Battelino T, Trebusak Podkrajsek K. Tesovnik T, et al. Among authors: hovnik t. Zdr Varst. 2015 Mar 13;54(2):74-8. doi: 10.1515/sjph-2015-0011. eCollection 2015 Jun. Zdr Varst. 2015. PMID: 27646911 Free PMC article.

9

Genetic polymorphisms in genes encoding antioxidant enzymes are associated with diabetic retinopathy in type 1 diabetes.

Hovnik T, Dolzan V, Bratina NU, Podkrajsek KT, Battelino T. Hovnik T, et al. Diabetes Care. 2009 Dec;32(12):2258-62. doi: 10.2337/dc09-0852. Epub 2009 Sep 14. Diabetes Care. 2009. PMID: 19752172 Free PMC article.

10

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

Bertok S, Žerjav Tanšek M, Kotnik P, Battelino T, Volk M, Pecile V, Cleva L, Gasparini P, Kovač J, Hovnik T. Bertok S, et al. Among authors: hovnik t. Zdr Varst. 2015 Mar 13;54(2):69-73. doi: 10.1515/sjph-2015-0010. eCollection 2015 Jun. Zdr Varst. 2015. PMID: 27646910 Free PMC article.

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