Şıklar Z - Search Results

1

Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations.

Cohen E, Belkacem S, Fedala S, Collot N, Khallouf E, Dastot F, Polak M, Duquesnoy P, Brioude F, Rose S, Viot G, Soleyan A, Carel JC, Sobrier ML, Chanson P, Gatelais F, Heinrichs C, Kaffel N, Coutant R, Savaş Erdeve Ş, Kurnaz E, Aycan Z, Thalassinos C, Lyonnet S, Şıklar Z, Berberoglu M, Brachet C, Amselem S, Legendre M. Cohen E, et al. Among authors: siklar z. Hum Mutat. 2019 Nov;40(11):2033-2043. doi: 10.1002/humu.23847. Epub 2019 Aug 6. Hum Mutat. 2019. PMID: 31231873

2

Latent autoimmune diabetes mellitus in children (LADC) with autoimmune thyroiditis and Celiac disease.

Aycan Z, Berberoglu M, Adiyaman P, Ergür AT, Ensari A, Evliyaoglu O, Siklar Z, Ocal G. Aycan Z, et al. Among authors: siklar z. J Pediatr Endocrinol Metab. 2004 Nov;17(11):1565-9. doi: 10.1515/jpem.2004.17.11.1565. J Pediatr Endocrinol Metab. 2004. PMID: 15570995

3

Incidence of iodine deficiency in patients presenting with goitre--discrepancy between clinical and ultrasonographic evaluation of the thyroid: comparison of patients with and without autoimmune thyroiditis--clinical, hormonal and urinary iodine excretion studies.

Evliyaoglu O, Berberoglu M, Adiyaman P, Aycan Z, Ergur A, Siklar Z, Ocal G, Fitoz S. Evliyaoglu O, et al. Among authors: siklar z. J Pediatr Endocrinol Metab. 2006 Jan;19(1):39-44. doi: 10.1515/jpem.2006.19.1.39. J Pediatr Endocrinol Metab. 2006. PMID: 16509527

4

Importance of thyroglobulin levels for diagnosis and monitoring of follicular thyroid carcinoma in an adolescent with severe iodine deficiency.

Siklar Z, Ocal G, Berberoğlu M, Adiyaman P, Ergür AT, Evliyaoğlu O, Sak SD. Siklar Z, et al. J Pediatr Endocrinol Metab. 2006 Sep;19(9):1175-8. doi: 10.1515/jpem.2006.19.9.1175. J Pediatr Endocrinol Metab. 2006. PMID: 17128567

5

Functional ovarian hyperandrogenism and polycystic ovary syndrome in prepubertal girls with obesity and/or premature pubarche.

Siklar Z, Oçal G, Adiyaman P, Ergur A, Berberoğlu M. Siklar Z, et al. J Pediatr Endocrinol Metab. 2007 Apr;20(4):475-81. doi: 10.1515/jpem.2007.20.4.475. J Pediatr Endocrinol Metab. 2007. PMID: 17550211

6

Disorders of gonadal development: a broad clinical, cytogenetic and histopathologic spectrum.

Siklar Z, Berberoğlu M, Adiyaman P, Salih M, Tükün A, Cetinkaya E, Aycan Z, Evliyaoğlu O, Ergur AT, Oçal G. Siklar Z, et al. Pediatr Endocrinol Rev. 2007 Mar;4(3):210-7. Pediatr Endocrinol Rev. 2007. PMID: 17551482

7

Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome.

Ergür AT, Ocal G, Berberoglu M, Tekin M, Kiliç BG, Aycan Z, Kutlu A, Adiyaman P, Siklar Z, Akar N, Sahin A, Akçayöz D. Ergür AT, et al. Among authors: siklar z. Pediatr Int. 2008 Apr;50(2):172-4. doi: 10.1111/j.1442-200X.2008.02540.x. Pediatr Int. 2008. PMID: 18353053

8

Persistently raised thyroid stimulating hormone in adequately treated congenital hypothyroidism on long-term follow-up.

Kara C, Ocal G, Berberoğlu M, Siklar Z, Adiyaman P. Kara C, et al. Among authors: siklar z. J Pediatr Endocrinol Metab. 2008 Mar;21(3):251-6. doi: 10.1515/jpem.2008.21.3.251. J Pediatr Endocrinol Metab. 2008. PMID: 18540252 Clinical Trial.

9

Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey.

Sadeghi F, Yurur-Kutlay N, Berberoglu M, Cetinkaya E, Aycan Z, Kara C, Ilgin Ruhi H, Ocal G, Siklar Z, Elhan A, Tukun A. Sadeghi F, et al. Among authors: siklar z. J Pediatr Endocrinol Metab. 2008 Aug;21(8):781-7. doi: 10.1515/jpem.2008.21.8.781. J Pediatr Endocrinol Metab. 2008. PMID: 18825878

10

Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesis.

Ocal G, Berberoğlu M, Siklar Z, Bilir P. Ocal G, et al. Among authors: siklar z. Exp Clin Endocrinol Diabetes. 2009 Jun;117(6):301-4. doi: 10.1055/s-0028-1085999. Epub 2008 Oct 1. Exp Clin Endocrinol Diabetes. 2009. PMID: 19085701

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