Yılmaz C - Search Results

1

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration.

Schaffer AE, Breuss MW, Caglayan AO, Al-Sanaa N, Al-Abdulwahed HY, Kaymakçalan H, Yılmaz C, Zaki MS, Rosti RO, Copeland B, Baek ST, Musaev D, Scott EC, Ben-Omran T, Kariminejad A, Kayserili H, Mojahedi F, Kara M, Cai N, Silhavy JL, Elsharif S, Fenercioglu E, Barshop BA, Kara B, Wang R, Stanley V, James KN, Nachnani R, Kalur A, Megahed H, Incecik F, Danda S, Alanay Y, Faqeih E, Melikishvili G, Mansour L, Miller I, Sukhudyan B, Chelly J, Dobyns WB, Bilguvar K, Jamra RA, Gunel M, Gleeson JG. Schaffer AE, et al. Among authors: yilmaz c. Nat Genet. 2018 Aug;50(8):1093-1101. doi: 10.1038/s41588-018-0166-0. Epub 2018 Jul 16. Nat Genet. 2018. PMID: 30013181 Free PMC article.

2

Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalities.

Radmanesh F, Caglayan AO, Silhavy JL, Yilmaz C, Cantagrel V, Omar T, Rosti B, Kaymakcalan H, Gabriel S, Li M, Sestan N, Bilguvar K, Dobyns WB, Zaki MS, Gunel M, Gleeson JG. Radmanesh F, et al. Among authors: yilmaz c. Am J Hum Genet. 2013 Mar 7;92(3):468-74. doi: 10.1016/j.ajhg.2013.02.005. Am J Hum Genet. 2013. PMID: 23472759 Free PMC article.

3

Rapidly progressive renal disease as part of Wolfram syndrome in a large inbred Turkish family due to a novel WFS1 mutation (p.Leu511Pro).

Yuca SA, Rendtorff ND, Boulahbel H, Lodahl M, Tranebjærg L, Cesur Y, Dogan M, Yilmaz C, Akgun C, Acikgoz M. Yuca SA, et al. Among authors: yilmaz c. Eur J Med Genet. 2012 Jan;55(1):37-42. doi: 10.1016/j.ejmg.2011.08.005. Epub 2011 Sep 23. Eur J Med Genet. 2012. PMID: 21968327

4

Prevalence of overweight and obesity in children and adolescents in eastern Turkey.

Yuca SA, Yılmaz C, Cesur Y, Doğan M, Kaya A, Başaranoğlu M. Yuca SA, et al. Among authors: yilmaz c. J Clin Res Pediatr Endocrinol. 2010;2(4):159-63. doi: 10.4274/jcrpe.v2i4.159. Epub 2010 Nov 5. J Clin Res Pediatr Endocrinol. 2010. PMID: 21274316 Free PMC article.

5

Vitamin D deficiency rickets in infants presenting with hypocalcaemic convulsions.

Cesur Y, Yuca SA, Kaya A, Yilmaz C, Bay A. Cesur Y, et al. Among authors: yilmaz c. West Indian Med J. 2013 Mar;62(3):201-4. West Indian Med J. 2013. PMID: 24564040

6

Surgical treatment outcome of subdural empyema: A clinical study.

Yilmaz N, Kiymaz N, Yilmaz C, Bay A, Yuca SA, Mumcu C, Caksen H. Yilmaz N, et al. Among authors: yilmaz c. Pediatr Neurosurg. 2006;42(5):293-8. doi: 10.1159/000094065. Pediatr Neurosurg. 2006. PMID: 16902341

7

Rubinstein-Taybi syndrome and CREBBP c.201 202delTA mutation: a case presenting with varicella meningoencephalitis.

Çaksen H, Bartsch O, Okur M, Temel H, Açikgoz M, Yilmaz C. Çaksen H, et al. Among authors: yilmaz c. Genet Couns. 2009;20(3):255-60. Genet Couns. 2009. PMID: 19852432

8

Evaluation of Lymphocyte Subgroups in Children With Down Syndrome.

Yılmaz C, Doğan M, Başarslan F, Yılmaz N, Yuca S, Bulan K, Kaya A, Çaksen H. Yılmaz C, et al. Among authors: yilmaz n. Clin Appl Thromb Hemost. 2015 Sep;21(6):546-9. doi: 10.1177/1076029613511521. Epub 2013 Nov 14. Clin Appl Thromb Hemost. 2015. PMID: 24243939 Free article.

9

Intracranial hemorrhage due to vitamin K deficiency in infants: a clinical study.

Yilmaz C, Yuca SA, Yilmaz N, Bektaş MS, Caksen H. Yilmaz C, et al. Among authors: yilmaz n. Int J Neurosci. 2009;119(12):2250-6. doi: 10.3109/00207450903170437. Int J Neurosci. 2009. PMID: 19916853

10

Acute amitriptyline intoxication: an analysis of 44 children.

Caksen H, Akbayram S, Odabaş D, Ozbek H, Erol M, Akgün C, Tuncer O, Yilmaz C. Caksen H, et al. Among authors: yilmaz c. Hum Exp Toxicol. 2006 Mar;25(3):107-10. doi: 10.1191/0960327106ht511oa. Hum Exp Toxicol. 2006. PMID: 16634328

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