Akinci A - Search Results

1

A novel ERCC6 splicing variant associated with a mild Cockayne syndrome phenotype.

Swartz JM, Akinci A, Andrew SF, Siğirci A, Hirschhorn JN, Rosenfeld RG, Dauber A, Hwa V. Swartz JM, et al. Among authors: akinci a. Horm Res Paediatr. 2014;82(5):344-52. doi: 10.1159/000368192. Epub 2014 Nov 1. Horm Res Paediatr. 2014. PMID: 25376329 Free PMC article.

2

Neutropenic enterocolitis (typhlitis) associated with infectious mononucleosis.

Siğirci A, Akinci A, Ozgen U, Ozen M. Siğirci A, et al. Among authors: akinci a. Pediatr Radiol. 2006 Feb;36(2):155-7. doi: 10.1007/s00247-005-0014-0. Epub 2005 Oct 29. Pediatr Radiol. 2006. PMID: 16258744

3

A novel exonic GHR splicing mutation (c.784G > C) in a patient with classical growth hormone insensitivity syndrome.

Akıncı A, Rosenfeld RG, Hwa V. Akıncı A, et al. Horm Res Paediatr. 2013;79(1):32-8. doi: 10.1159/000341527. Epub 2012 Sep 20. Horm Res Paediatr. 2013. PMID: 23006617

4

A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment.

Çamtosun E, Akıncı A, Demiral E, Tekedereli İ, Sığırcı A. Çamtosun E, et al. Among authors: akinci a. J Clin Res Pediatr Endocrinol. 2019 Sep 3;11(3):301-305. doi: 10.4274/jcrpe.galenos.2018.2018.0211. Epub 2018 Nov 23. J Clin Res Pediatr Endocrinol. 2019. PMID: 30468148 Free PMC article.

5

Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries.

Akinci A, Karakurt C, Hwa V, Dündar I, Çamtosun E. Akinci A, et al. Cardiovasc J Afr. 2019 Mar/Apr 23;30(2):e7-e8. doi: 10.5830/CVJA-2019-002. Epub 2019 Jan 22. Cardiovasc J Afr. 2019. PMID: 30720842

6

Evaluation of visceral adipose tissue thickness in precocious puberty.

Taşolar SD, Siğirci A, Çiftçi N, Cengiz A, Doğan GM, Akinci A. Taşolar SD, et al. Among authors: akinci a. Eur Rev Med Pharmacol Sci. 2023 Oct;27(19):9226-9233. doi: 10.26355/eurrev_202310_33950. Eur Rev Med Pharmacol Sci. 2023. PMID: 37843336 Free article.

7

46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report.

Çiftci N, Kayaş L, Çamtosun E, Akıncı A. Çiftci N, et al. Among authors: akinci a. J Clin Res Pediatr Endocrinol. 2022 Jun 7;14(2):233-238. doi: 10.4274/jcrpe.galenos.2020.2020.0249. Epub 2021 Jan 4. J Clin Res Pediatr Endocrinol. 2022. PMID: 33389920 Free PMC article.

8

Prune-belly syndrome and pulmonary hypoplasia: a potential cause of death.

Soylu H, Kutlu NO, Sönmezgöz E, Bükte Y, Ozgen U, Akinci A. Soylu H, et al. Among authors: akinci a. Pediatr Int. 2001 Apr;43(2):172-5. doi: 10.1046/j.1442-200x.2001.01347.x. Pediatr Int. 2001. PMID: 11285073 No abstract available.

9

A Chryseobacterium meningosepticum outbreak in a neonatal ward.

Güngör S, Ozen M, Akinci A, Durmaz R. Güngör S, et al. Among authors: akinci a. Infect Control Hosp Epidemiol. 2003 Aug;24(8):613-7. doi: 10.1086/502261. Infect Control Hosp Epidemiol. 2003. PMID: 12940584

10

The role of ghrelin in weight gain and growth in epileptic children using valproate.

Gungor S, Yücel G, Akinci A, Tabel Y, Ozerol IH, Yologlu S. Gungor S, et al. Among authors: akinci a. J Child Neurol. 2007 Dec;22(12):1384-8. doi: 10.1177/0883073807307096. J Child Neurol. 2007. PMID: 18174556 Clinical Trial.

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