Battelino T - Search Results

1

Integrating Genetic Insights, Technological Advancements, Screening, and Personalized Pharmacological Interventions in Childhood Obesity.

Šket R, Slapnik B, Kotnik P, Črepinšek K, Čugalj Kern B, Tesovnik T, Jenko Bizjan B, Vrhovšek B, Remec ŽI, Debeljak M, Battelino T, Kovač J. Šket R, et al. Among authors: battelino t. Adv Ther. 2024 Nov 13. doi: 10.1007/s12325-024-03057-8. Online ahead of print. Adv Ther. 2024. PMID: 39535684 Review.

2

Goiter prevalence and urinary iodine concentration in Slovenian adolescents.

Kotnik P, Sirca Campa A, Zupancic M, Stimec M, Smole K, Mis NF, Battelino T, Krzisnik C. Kotnik P, et al. Among authors: battelino t. Thyroid. 2006 Aug;16(8):769-73. doi: 10.1089/thy.2006.16.769. Thyroid. 2006. PMID: 16910879

3

High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis.

Avbelj M, Tahirovic H, Debeljak M, Kusekova M, Toromanovic A, Krzisnik C, Battelino T. Avbelj M, et al. Among authors: battelino t. Eur J Endocrinol. 2007 May;156(5):511-9. doi: 10.1530/EJE-07-0037. Eur J Endocrinol. 2007. PMID: 17468186

4

Correlation between AVPR2 mutations and urinary AQP2 excretion in patients with nephrogenic diabetes insipidus.

Kotnik P, Battelino T, Debeljak M, Podkrajsek KT, Waldhauser F, Frøkiaer J, Nielsen S, Krzisnik C. Kotnik P, et al. Among authors: battelino t. J Pediatr Endocrinol Metab. 2007 Apr;20(4):483-9. doi: 10.1515/jpem.2007.20.4.483. J Pediatr Endocrinol Metab. 2007. PMID: 17550212

5

Iodine intake of Slovenian adolescents.

Stimec M, Mis NF, Smole K, Sirca-Campa A, Kotnik P, Zupancic M, Battelino T, Krizisnik C. Stimec M, et al. Among authors: battelino t. Ann Nutr Metab. 2007;51(5):439-47. doi: 10.1159/000111164. Epub 2007 Nov 20. Ann Nutr Metab. 2007. PMID: 18025817

6

Adequate iodine intake of Slovenian adolescents is primarily attributed to excessive salt intake.

Stimec M, Kobe H, Smole K, Kotnik P, Sirca-Campa A, Zupancic M, Battelino T, Krzisnik C, Fidler Mis N. Stimec M, et al. Among authors: battelino t. Nutr Res. 2009 Dec;29(12):888-96. doi: 10.1016/j.nutres.2009.10.011. Nutr Res. 2009. PMID: 19963163

7

Lack of association of common allelic variants in the thyroglobulin gene with Hashimoto's thyroiditis in young subjects with type 1 diabetes.

Kotnik P, Debeljak M, Avbelj M, Hovnik T, Ursic Bratina N, Krzisnik C, Battelino T. Kotnik P, et al. Among authors: battelino t. Horm Res Paediatr. 2010;73(4):244-7. doi: 10.1159/000284388. Epub 2010 Mar 9. Horm Res Paediatr. 2010. PMID: 20215770

8

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: battelino t. Ophthalmic Genet. 2012 Sep;33(3):167-70. doi: 10.3109/13816810.2011.559651. Epub 2012 Apr 9. Ophthalmic Genet. 2012. PMID: 22486324

9

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: battelino 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

10

Cathepsin C gene 5'-untranslated region mutation in papillon-lefèvre syndrome.

Kosem R, Debeljak M, Repič Lampret B, Kansky A, Battelino T, Trebušak Podkrajšek K. Kosem R, et al. Among authors: battelino t. Dermatology. 2012;225(3):193-203. doi: 10.1159/000342509. Epub 2012 Oct 27. Dermatology. 2012. PMID: 23108224

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