Dursun F - Search Results

1

Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2.

Dursun F, Turan İ, Bitkin EÇ, Bayramoğlu E, Çayır A, Erdeve ŞS, Çakır EDP, Çamtosun E, Dilek SO, Kırmızıbekmez H, Eser M, Türkyılmaz A, Karagüzel G. Dursun F, et al. Clin Endocrinol (Oxf). 2024 Feb 7. doi: 10.1111/cen.15028. Online ahead of print. Clin Endocrinol (Oxf). 2024. PMID: 38324408

2

Developmental defects of the thyroid gland: relationship with advanced maternal age.

Kirmızibekmez H, Güven A, Yildiz M, Cebeci AN, Dursun F. Kirmızibekmez H, et al. Among authors: dursun f. J Clin Res Pediatr Endocrinol. 2012 Jun;4(2):72-5. doi: 10.4274/jcrpe.560. J Clin Res Pediatr Endocrinol. 2012. PMID: 22672863 Free PMC article.

3

Clinical features and management of diabetic ketoacidosis in different age groups of children: children less than 5 years of age are at higher risk of metabolic decompensation.

Cebeci AN, Guven A, Kirmizibekmez H, Yildiz M, Dursun F. Cebeci AN, et al. Among authors: dursun f. J Pediatr Endocrinol Metab. 2012;25(9-10):917-25. doi: 10.1515/jpem-2012-0110. J Pediatr Endocrinol Metab. 2012. PMID: 23426821

4

Remission with cabergoline in adolescent boys with Cushing's disease.

Güven A, Baltacıoğlu F, Dursun F, Cebeci AN, Kırmızıbekmez H. Güven A, et al. Among authors: dursun f. J Clin Res Pediatr Endocrinol. 2013 Sep 10;5(3):194-8. doi: 10.4274/Jcrpe.1007. J Clin Res Pediatr Endocrinol. 2013. PMID: 24072089 Free PMC article.

5

Tamoxifen-associated hirsutism: an unusual side effect in a 5-year-old girl with McCune-Albright syndrome.

Kırmızıbekmez H, Yesiltepe Mutlu RG, Dursun F, İşgüven ŞP. Kırmızıbekmez H, et al. Among authors: dursun f. J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):1191-3. doi: 10.1515/jpem-2014-0437. J Pediatr Endocrinol Metab. 2015. PMID: 26024247

6

A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor.

Dursun F, Su Dur ŞM, Şahin C, Kırmızıbekmez H, Karabulut MH, Yörük A. Dursun F, et al. Case Rep Pediatr. 2015;2015:439239. doi: 10.1155/2015/439239. Epub 2015 Aug 23. Case Rep Pediatr. 2015. PMID: 26366315 Free PMC article.

7

A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family.

Dursun F, Mohamoud HS, Karim N, Naeem M, Jelani M, Kırmızıbekmez H. Dursun F, et al. J Clin Res Pediatr Endocrinol. 2016 Dec 1;8(4):472-477. doi: 10.4274/jcrpe.2717. Epub 2016 Apr 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 27087618 Free PMC article.

8

Iatrogenic Cushing's syndrome caused by intranasal steroid use.

Dursun F, Kirmizibekmez H. Dursun F, et al. North Clin Istanb. 2016 Apr 4;4(1):97-99. doi: 10.14744/nci.2016.38981. eCollection 2017. North Clin Istanb. 2016. PMID: 28752153 Free PMC article.

9

A rare cause of respiratory distress and edema in neonate: Panhypopituitarism.

Dursun F, Kirmizibekmez H, Metin F. Dursun F, et al. North Clin Istanb. 2017 Aug 26;4(2):188-191. doi: 10.14744/nci.2016.47450. eCollection 2017. North Clin Istanb. 2017. PMID: 28971179 Free PMC article.

10

Cholestasis and hypercalcemia secondary to panhypopituitarism in a newborn.

Dursun F, Gerenli N, Kırmızıbekmez H. Dursun F, et al. Turk J Pediatr. 2017;59(1):100-103. doi: 10.24953/turkjped.2017.01.020. Turk J Pediatr. 2017. PMID: 29168375 Free article.

Dursun F, Gerenli N, Kirmizibekmez H. Cholestasis and hypercalcemia secondary to panhypopituitarism in a newborn. ...

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