Cetincelik U - Search Results

1

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.

Malone AF, Phelan PJ, Hall G, Cetincelik U, Homstad A, Alonso AS, Jiang R, Lindsey TB, Wu G, Sparks MA, Smith SR, Webb NJ, Kalra PA, Adeyemo AA, Shaw AS, Conlon PJ, Jennette JC, Howell DN, Winn MP, Gbadegesin RA. Malone AF, et al. Among authors: cetincelik u. Kidney Int. 2014 Dec;86(6):1253-9. doi: 10.1038/ki.2014.305. Epub 2014 Sep 17. Kidney Int. 2014. PMID: 25229338 Free PMC article.

2

Vascular endothelial growth factor gene +813CC polymorphism of foetus is associated with preterm labour but not with pre-eclampsia in Turkish pregnant women.

Atis A, Oruc O, Aydin Y, Cetincelik U, Goker N. Atis A, et al. Among authors: cetincelik u. Int J Immunogenet. 2012 Jun;39(3):241-6. doi: 10.1111/j.1744-313X.2011.01082.x. Epub 2012 Jan 18. Int J Immunogenet. 2012. PMID: 22257487

3

Joubert syndrome and related disorders: a rare cause of intrahepatic portal hypertension in childhood.

Usta M, Urganci N, Özçelik G, Çetinçelik Ü, Kafadar I, Özgüven BY. Usta M, et al. Among authors: cetincelik u. Eur Rev Med Pharmacol Sci. 2015 Jun;19(12):2297-300. Eur Rev Med Pharmacol Sci. 2015. PMID: 26166658 Free article.

4

A new chromosomal arrangement due to paternal balanced translocation for syndromic oesophageal atresia: case report.

Bebek AK, Agar S, Aydın C, Erman S, Çetinçelik Ü, Dokucu Aİ. Bebek AK, et al. Among authors: cetincelik u. J Obstet Gynaecol. 2018 Apr;38(3):417-418. doi: 10.1080/01443615.2017.1357166. Epub 2017 Oct 11. J Obstet Gynaecol. 2018. PMID: 29017392 No abstract available.

5

Management of a Klippel-Trenaunay syndrome in pregnant women with mega-cisterna magna and splenic and vulvar varices at birth: a case report.

Atis A, Ozdemir G, Tuncer G, Cetincelik U, Goker N, Ozsoy S. Atis A, et al. Among authors: cetincelik u. J Obstet Gynaecol Res. 2012 Nov;38(11):1331-4. doi: 10.1111/j.1447-0756.2012.01867.x. Epub 2012 May 21. J Obstet Gynaecol Res. 2012. PMID: 22612590

6

The role of CYP1A1 Msp1 gene polymorphisms on lung cancer development in Turkey.

Demir A, Altin S, Demir I, Köksal V, Cetinçelik U, Dinçer I. Demir A, et al. Among authors: cetincelik u. Tuberk Toraks. 2005;53(1):5-9. Tuberk Toraks. 2005. PMID: 15765281

7

Familial Adult-onset Alexander Disease: Clinical and Neuroradiological Findings of Three Cases.

Elmali AD, Çetinçelik Ü, Işlak C, Uzun Adatepe N, Karaali Savrun F, Yalçinkaya C. Elmali AD, et al. Among authors: cetincelik u. Noro Psikiyatr Ars. 2016 Jun;53(2):169-172. doi: 10.5152/npa.2015.10193. Epub 2016 Jun 1. Noro Psikiyatr Ars. 2016. PMID: 28360791 Free PMC article.

8

Therapy-resistant leg ulcer in a patient with Rothmund-Thomson syndrome.

Altunay I, Fisek N, Gokdemir G, Sakız D, Cetincelik U. Altunay I, et al. Among authors: cetincelik u. Int Wound J. 2010 Dec;7(6):531-5. doi: 10.1111/j.1742-481X.2010.00734.x. Epub 2010 Sep 21. Int Wound J. 2010. PMID: 20860557 Free PMC article.

9

Facial dysmorphism in Leigh syndrome with SURF-1 mutation and COX deficiency.

Yüksel A, Seven M, Cetincelik U, Yeşil G, Köksal V. Yüksel A, et al. Among authors: cetincelik u. Pediatr Neurol. 2006 Jun;34(6):486-9. doi: 10.1016/j.pediatrneurol.2005.10.020. Pediatr Neurol. 2006. PMID: 16765830

10

Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants.

Hamilton EMC, Tekturk P, Cialdella F, van Rappard DF, Wolf NI, Yalcinkaya C, Çetinçelik Ü, Rajaee A, Kariminejad A, Paprocka J, Yapici Z, Bošnjak VM, van der Knaap MS; MLC Research Group. Hamilton EMC, et al. Among authors: cetincelik u. Neurology. 2018 Apr 17;90(16):e1395-e1403. doi: 10.1212/WNL.0000000000005334. Epub 2018 Mar 21. Neurology. 2018. PMID: 29661901 Free PMC article.

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