Battelino T - Search Results

1

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.

2

Incidence of childhood-onset Type I diabetes in Slovenia and the Tuzia region (Bosnia and Herzegovina) in the period 1990-1998.

Bratina NU, Tahirović H, Battelino T, Krzisnik C. Bratina NU, et al. Among authors: battelino t. Diabetologia. 2001 Oct;44 Suppl 3:B27-31. doi: 10.1007/pl00002949. Diabetologia. 2001. PMID: 11724412

3

The HLA-DRB, -DQB polymorphism and anti-insulin antibody response in Slovenian patients with type 1 diabetes.

Battelino T, Ursic-Bratina N, Dolzan V, Stopar-Obreza M, Pozzilli P, Krzisnik C, Vidan-Jeras B. Battelino T, et al. Eur J Immunogenet. 2003 Jun;30(3):223-7. doi: 10.1046/j.1365-2370.2003.00395.x. Eur J Immunogenet. 2003. PMID: 12787001

4

Mutational spectrum of congenital adrenal hyperplasia in Slovenian patients: a novel Ala15Thr mutation and Pro30Leu within a larger gene conversion associated with a severe form of the disease.

Dolzan V, Stopar-Obreza M, Zerjav-Tansek M, Breskvar K, Krzisnik C, Battelino T. Dolzan V, et al. Among authors: battelino t. Eur J Endocrinol. 2003 Aug;149(2):137-44. doi: 10.1530/eje.0.1490137. Eur J Endocrinol. 2003. PMID: 12887291

5

Autoimmune regulator-1 messenger ribonucleic acid analysis in a novel intronic mutation and two additional novel AIRE gene mutations in a cohort of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients.

Podkrajsek KT, Bratanic N, Krzisnik C, Battelino T. Podkrajsek KT, et al. Among authors: battelino t. J Clin Endocrinol Metab. 2005 Aug;90(8):4930-5. doi: 10.1210/jc.2005-0418. Epub 2005 May 10. J Clin Endocrinol Metab. 2005. PMID: 15886230

6

Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia.

Dolzan V, Sólyom J, Fekete G, Kovács J, Rakosnikova V, Votava F, Lebl J, Pribilincova Z, Baumgartner-Parzer SM, Riedl S, Waldhauser F, Frisch H, Stopar-Obreza M, Krzisnik C, Battelino T. Dolzan V, et al. Among authors: battelino t. Eur J Endocrinol. 2005 Jul;153(1):99-106. doi: 10.1530/eje.1.01944. Eur J Endocrinol. 2005. PMID: 15994751

7

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

8

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

9

Lifetime prevalence of suicidal and self-injurious behaviors in a representative cohort of Slovenian adolescents with type 1 diabetes.

Radobuljac MD, Bratina NU, Battelino T, Tomori M. Radobuljac MD, et al. Among authors: battelino t. Pediatr Diabetes. 2009 Nov;10(7):424-31. doi: 10.1111/j.1399-5448.2009.00501.x. Epub 2009 Apr 8. Pediatr Diabetes. 2009. PMID: 19490494

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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