Turkkahraman D - Search Results

Year	Number of Results
2006	2
2007	1
2008	3
2009	3
2010	2
2011	1
2012	1
2013	2
2014	4
2015	5
2016	4
2017	3
2018	2
2019	2
2020	1
2021	3
2022	2
2023	4
2024	1

1

Late-onset Van Wyk Grumbach syndrome without precocious puberty.

Tekin S, Gullu M, Turkkahraman D. Tekin S, et al. Among authors: turkkahraman d. Pediatr Int. 2023 Jan-Dec;65(1):e15661. doi: 10.1111/ped.15661. Pediatr Int. 2023. PMID: 37899538 No abstract available.

2

A Boy with 46,XX Karyotype (SRY double-positive) having a Leydig Cell Tumor.

Gullu M, Aydın S, Kalkan T, Pınarcı T, Turkkahraman D. Gullu M, et al. Among authors: turkkahraman d. J Clin Res Pediatr Endocrinol. 2023 Mar 29. doi: 10.4274/jcrpe.galenos.2023.2022-9-14. Online ahead of print. J Clin Res Pediatr Endocrinol. 2023. PMID: 36987810 Free article.

3

A novel EZH2 gene variant in a case of Weaver syndrome with postaxial polydactyly.

Turkkahraman D, Sakarya ANP, Randa NC. Turkkahraman D, et al. Am J Med Genet A. 2021 Jul;185(7):2234-2237. doi: 10.1002/ajmg.a.62189. Epub 2021 Mar 31. Am J Med Genet A. 2021. PMID: 33788986 No abstract available.

4

Serum Ghrelin and Glukagon-like Peptid 1 Levels in Children with Prader-Willi and Bardet-Biedl Syndromes.

Turkkahraman D, Tekin S, Gullu M, Aykal G. Turkkahraman D, et al. J Clin Res Pediatr Endocrinol. 2023 Dec 15. doi: 10.4274/jcrpe.galenos.2023.2023-7-7. Online ahead of print. J Clin Res Pediatr Endocrinol. 2023. PMID: 38099591 Free article.

5

A Large PROP1 Gene Deletion in a Turkish Pedigree.

Gorar S, Turkkahraman D, Yararbas K. Gorar S, et al. Among authors: turkkahraman d. Case Rep Endocrinol. 2018 Mar 14;2018:2403430. doi: 10.1155/2018/2403430. eCollection 2018. Case Rep Endocrinol. 2018. PMID: 30112224 Free PMC article.

6

Serum alpha-melanocyte-stimulating hormone (a-MSH), brain-derived neurotrophic factor (BDNF), and agouti-related protein (AGRP) levels in children with Prader-Willi or Bardet-Biedl syndromes.

Turkkahraman D, Sirazi EC, Aykal G. Turkkahraman D, et al. J Endocrinol Invest. 2022 May;45(5):1031-1037. doi: 10.1007/s40618-021-01737-8. Epub 2022 Jan 31. J Endocrinol Invest. 2022. PMID: 35098494

7

Genomic analysis to screen potential genes and mutations in children with non-syndromic early onset severe obesity: a multicentre study in Turkey.

Akinci A, Kara A, Özgür A, Turkkahraman D, Aksu S. Akinci A, et al. Among authors: turkkahraman d. Mol Biol Rep. 2022 Mar;49(3):1883-1893. doi: 10.1007/s11033-021-06999-2. Epub 2021 Nov 30. Mol Biol Rep. 2022. PMID: 34850337

8

CTLA-4 (+49A/G) polymorphism and type-1 diabetes in Turkish children.

Çelmeli F, Türkkahraman D, Özel D, Akçurin S, Yegin O. Çelmeli F, et al. Among authors: turkkahraman d. J Clin Res Pediatr Endocrinol. 2013;5(1):40-3. doi: 10.4274/Jcrpe.879. Epub 2013 Jul 1. J Clin Res Pediatr Endocrinol. 2013. PMID: 23367498 Free PMC article.

9

A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in IGSF1 Gene.

Türkkahraman D, Karataş Torun N, Randa NC. Türkkahraman D, et al. J Clin Res Pediatr Endocrinol. 2021 Aug 23;13(3):353-357. doi: 10.4274/jcrpe.galenos.2020.2020.0149. Epub 2020 Aug 10. J Clin Res Pediatr Endocrinol. 2021. PMID: 32772515 Free PMC article.

10

Novel inactivating mutations of the DCAF17 gene in American and Turkish families cause male infertility and female subfertility in the mouse model.

Gurbuz F, Desai S, Diao F, Turkkahraman D, Wranitz F, Wood-Trageser M, Shin YH, Kotan LD, Jiang H, Witchel S, Gurtunca N, Yatsenko S, Mysliwec D, Topaloglu K, Rajkovic A. Gurbuz F, et al. Among authors: turkkahraman d. Clin Genet. 2018 Apr;93(4):853-859. doi: 10.1111/cge.13183. Epub 2018 Jan 24. Clin Genet. 2018. PMID: 29178422

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