Battelino T - Search Results

1

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

Stritar J, Stavber L, Ficko M, Kotnik P, Battelino T, Trebušak Podkrajšek K, Hovnik T. Stritar J, et al. Among authors: battelino t. Genes (Basel). 2021 Sep 29;12(10):1546. doi: 10.3390/genes12101546. Genes (Basel). 2021. PMID: 34680940 Free PMC article.

2

A novel mutation in the G4.5 (TAZ) gene in a kindred with Barth syndrome.

Vesel S, Stopar-Obreza M, Trebusak-Podkrajsek K, Jazbec J, Podnar T, Battelino T. Vesel S, et al. Among authors: battelino t. Eur J Hum Genet. 2003 Jan;11(1):97-101. doi: 10.1038/sj.ejhg.5200926. Eur J Hum Genet. 2003. PMID: 12529714

3

A novel L94Q mutation in the CDKN2A gene in a melanoma kindred.

Avbelj M, Hocevar M, Trebusak-Podkrajsek K, Krzisnik C, Battelino T. Avbelj M, et al. Among authors: battelino t. Melanoma Res. 2003 Dec;13(6):567-70. doi: 10.1097/01.cmr.0000056289.15046.c0. Melanoma Res. 2003. PMID: 14646619

4

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

5

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

6

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

7

Detection of a complete autoimmune regulator gene deletion and two additional novel mutations in a cohort of patients with atypical phenotypic variants of autoimmune polyglandular syndrome type 1.

Podkrajsek KT, Milenković T, Odink RJ, Claasen-van der Grinten HL, Bratanic N, Hovnik T, Battelino T. Podkrajsek KT, et al. Among authors: battelino t. Eur J Endocrinol. 2008 Nov;159(5):633-9. doi: 10.1530/EJE-08-0328. Epub 2008 Aug 5. Eur J Endocrinol. 2008. PMID: 18682433

8

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. Among authors: battelino t. 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.

9

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

10

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

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