Petkovic V - Search Results

1

Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiency.

Petkovic V, Lochmatter D, Turton J, Clayton PE, Trainer PJ, Dattani MT, Eblé A, Robinson IC, Flück CE, Mullis PE. Petkovic V, et al. J Clin Endocrinol Metab. 2007 Nov;92(11):4427-35. doi: 10.1210/jc.2007-0857. Epub 2007 Aug 28. J Clin Endocrinol Metab. 2007. PMID: 17726075

2

Evaluation of the biological activity of a growth hormone (GH) mutant (R77C) and its impact on GH responsiveness and stature.

Petkovic V, Besson A, Thevis M, Lochmatter D, Eblé A, Flück CE, Mullis PE. Petkovic V, et al. J Clin Endocrinol Metab. 2007 Aug;92(8):2893-901. doi: 10.1210/jc.2006-2238. Epub 2007 May 22. J Clin Endocrinol Metab. 2007. PMID: 17519310

3

GH mutant (R77C) in a pedigree presenting with the delay of growth and pubertal development: structural analysis of the mutant and evaluation of the biological activity.

Petkovic V, Thevis M, Lochmatter D, Besson A, Eblé A, Flück CE, Mullis PE. Petkovic V, et al. Eur J Endocrinol. 2007 Aug;157 Suppl 1:S67-74. doi: 10.1530/EJE-07-0339. Eur J Endocrinol. 2007. PMID: 17785701

4

Influence of growth hormone (GH) receptor deletion of exon 3 and full-length isoforms on GH response and final height in patients with severe GH deficiency.

Räz B, Janner M, Petkovic V, Lochmatter D, Eblé A, Dattani MT, Hindmarsh PC, Flück CE, Mullis PE. Räz B, et al. Among authors: petkovic v. J Clin Endocrinol Metab. 2008 Mar;93(3):974-80. doi: 10.1210/jc.2007-1382. Epub 2007 Nov 20. J Clin Endocrinol Metab. 2008. PMID: 18029459 Free article.

5

Growth hormone (GH) deficiency type II: a novel GH-1 gene mutation (GH-R178H) affecting secretion and action.

Petkovic V, Godi M, Pandey AV, Lochmatter D, Buchanan CR, Dattani MT, Eblé A, Flück CE, Mullis PE. Petkovic V, et al. J Clin Endocrinol Metab. 2010 Feb;95(2):731-9. doi: 10.1210/jc.2009-1247. Epub 2009 Dec 1. J Clin Endocrinol Metab. 2010. PMID: 19952226

6

Growth hormone (GH)-releasing hormone increases the expression of the dominant-negative GH isoform in cases of isolated GH deficiency due to GH splice-site mutations.

Petkovic V, Godi M, Lochmatter D, Eblé A, Flück CE, Robinson IC, Mullis PE. Petkovic V, et al. Endocrinology. 2010 Jun;151(6):2650-8. doi: 10.1210/en.2009-1280. Epub 2010 Mar 29. Endocrinology. 2010. PMID: 20351314

7

Isolated GH deficiency type II: knockdown of the harmful Delta3GH recovers wt-GH secretion in rat tumor pituitary cells.

Lochmatter D, Strom M, Eblé A, Petkovic V, Flück CE, Bidlingmaier M, Robinson IC, Mullis PE. Lochmatter D, et al. Among authors: petkovic v. Endocrinology. 2010 Sep;151(9):4400-9. doi: 10.1210/en.2010-0196. Epub 2010 Jun 30. Endocrinology. 2010. PMID: 20591972

8

A novel GH-1 gene mutation (GH-P59L) causes partial GH deficiency type II combined with bioinactive GH syndrome.

Petkovic V, Eblé A, Pandey AV, Betta M, Mella P, Flück CE, Buzi F, Mullis PE. Petkovic V, et al. Growth Horm IGF Res. 2011 Jun;21(3):160-6. doi: 10.1016/j.ghir.2011.04.002. Epub 2011 May 4. Growth Horm IGF Res. 2011. PMID: 21546299

9

Association of the (CA)n repeat polymorphism of insulin-like growth factor-I and -202 A/C IGF-binding protein-3 promoter polymorphism with adult height in patients with severe growth hormone deficiency.

Miletta MC, Scheidegger UA, Giordano M, Bozzola M, Pagani S, Bona G, Dattani M, Hindmarsh PC, Petkovic V, Oser-Meier M, Flück CE, Mullis PE. Miletta MC, et al. Among authors: petkovic v. Clin Endocrinol (Oxf). 2012 May;76(5):683-90. doi: 10.1111/j.1365-2265.2011.04267.x. Clin Endocrinol (Oxf). 2012. PMID: 22026507

10

Short stature in two siblings heterozygous for a novel bioinactive GH mutant (GH-P59S) suggesting that the mutant also affects secretion of the wild-type GH.

Petkovic V, Miletta MC, Boot AM, Losekoot M, Flück CE, Pandey AV, Eblé A, Wit JM, Mullis PE. Petkovic V, et al. Eur J Endocrinol. 2013 Feb 15;168(3):K35-43. doi: 10.1530/EJE-12-0847. Print 2013 Mar. Eur J Endocrinol. 2013. PMID: 23417163

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