Atay Z - Search Results

1

Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features.

Arman A, Bereket A, Coker A, Kiper PÖ, Güran T, Ozkan B, Atay Z, Akçay T, Haliloglu B, Boduroglu K, Alanay Y, Turan S. Arman A, et al. Among authors: atay z. Orphanet J Rare Dis. 2014 Apr 26;9:60. doi: 10.1186/1750-1172-9-60. Orphanet J Rare Dis. 2014. PMID: 24767306 Free PMC article.

2

Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor.

Guran T, Tolhurst G, Bereket A, Rocha N, Porter K, Turan S, Gribble FM, Kotan LD, Akcay T, Atay Z, Canan H, Serin A, O'Rahilly S, Reimann F, Semple RK, Topaloglu AK. Guran T, et al. Among authors: atay z. J Clin Endocrinol Metab. 2009 Oct;94(10):3633-3639. doi: 10.1210/jc.2009-0551. Epub 2009 Sep 15. J Clin Endocrinol Metab. 2009. PMID: 19755480 Free PMC article.

3

Radiologic and hormonal evaluation of pituitary abnormalities in patients with Bardet-Biedl syndrome.

Guran T, Ekinci G, Atay Z, Turan S, Akcay T, Bereket A. Guran T, et al. Among authors: atay z. Clin Dysmorphol. 2011 Jan;20(1):26-31. doi: 10.1097/MCD.0b013e32833fd528. Clin Dysmorphol. 2011. PMID: 20966747

4

Prevalence of type 1 diabetes mellitus in 6-18-yr-old school children living in Istanbul, Turkey.

Akesen E, Turan S, Güran T, Atay Z, Save D, Bereket A. Akesen E, et al. Among authors: atay z. Pediatr Diabetes. 2011 Sep;12(6):567-71. doi: 10.1111/j.1399-5448.2010.00744.x. Epub 2011 Mar 21. Pediatr Diabetes. 2011. PMID: 21418453

5

Serum alkaline phosphatase levels in healthy children and evaluation of alkaline phosphatase z-scores in different types of rickets.

Turan S, Topcu B, Gökçe İ, Güran T, Atay Z, Omar A, Akçay T, Bereket A. Turan S, et al. Among authors: atay z. J Clin Res Pediatr Endocrinol. 2011;3(1):7-11. doi: 10.4274/jcrpe.v3i1.02. Epub 2011 Feb 23. J Clin Res Pediatr Endocrinol. 2011. PMID: 21448327 Free PMC article.

6

Cognitive and psychosocial development in children with familial hypomagnesaemia.

Guran T, Arman A, Akcay T, Kayan E, Atay Z, Turan S, Bereket A. Guran T, et al. Among authors: atay z. Magnes Res. 2011 Mar;24(1):7-12. doi: 10.1684/mrh.2011.0278. Magnes Res. 2011. PMID: 21489917 Free article.

7

Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes.

Guran T, Akcay T, Bereket A, Atay Z, Turan S, Haisch L, Konrad M, Schlingmann KP. Guran T, et al. Among authors: atay z. Nephrol Dial Transplant. 2012 Feb;27(2):667-73. doi: 10.1093/ndt/gfr300. Epub 2011 Jun 9. Nephrol Dial Transplant. 2012. PMID: 21669885

8

Puberty and influencing factors in schoolgirls living in Istanbul: end of the secular trend?

Atay Z, Turan S, Guran T, Furman A, Bereket A. Atay Z, et al. Pediatrics. 2011 Jul;128(1):e40-5. doi: 10.1542/peds.2010-2267. Epub 2011 Jun 13. Pediatrics. 2011. PMID: 21669888

9

The prevalence and risk factors of premature thelarche and pubarche in 4- to 8-year-old girls.

Atay Z, Turan S, Guran T, Furman A, Bereket A. Atay Z, et al. Acta Paediatr. 2012 Feb;101(2):e71-5. doi: 10.1111/j.1651-2227.2011.02444.x. Epub 2011 Sep 23. Acta Paediatr. 2012. PMID: 21854448

10

An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).

Turan S, Hughes C, Atay Z, Guran T, Haliloglu B, Clark AJ, Bereket A, Metherell LA. Turan S, et al. Among authors: atay z. J Clin Endocrinol Metab. 2012 May;97(5):E771-4. doi: 10.1210/jc.2011-2414. Epub 2012 Feb 15. J Clin Endocrinol Metab. 2012. PMID: 22337906 Free PMC article.

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