1. Apo E genotype and cerebral palsy. (June 2017) Authors: Gumus, Evren; Cilingir, Oguz; Yarar, Coskun; Carman, Kursat Bora; Ozdemir, Muhsin; Kocak, Ozan; Gurlevik, Sibel Lacinel; Artan, Sevlhan; Aras, Beyhan Durak Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e72 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Congenital amegakaryocytic thrombocytopenia with severe neurological findings. Issue 8 (December 2016) Authors: Bör, Özcan; Turhan, Ayse B.; Yarar, Coskun Journal: Blood coagulation and fibrinolysis Issue: Volume 27:Issue 8(2016) Page Start: 936 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Congenital amegakaryocytic thrombocytopenia with severe neurological findings. Issue 8 (December 2016) Authors: Bör, Özcan; Turhan, Ayse B.; Yarar, Coskun Journal: Blood coagulation and fibrinolysis Issue: Volume 27:Issue 8(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Evaluation of immunization status in children with chronic neurological disease. (June 2017) Authors: Dinleyici, Meltam; Carman, Kursat Bora; Yarar, Coskun; Gurlevik, Sibel Lacinel; Kilic, Omer; Dinleyici, Ener Cagri Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e199 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Evaluation of micronutrient levels in children with cerebral palsy. Issue 1 (5th May 2022) Authors: Carman, Kursat Bora; Aydın, Kursad; Kilic Aydin, Betul; Cansu, Ali; Direk, Meltem Cobanogullari; Durmus, Selver; Dündar, Nihal Olgaç; Gencpinar, Pinar; Gungor, Serdal; Gurkas, Esra; Hur, Ozgen; Karadag, Meral; Karademir, Cefa Nil; Ozkan Kart, Pinar; Okuyaz, Cetin; Oz, Nefise Arıbas; Peduk, Yakup;... Journal: Pediatrics international Issue: Volume 64:Issue 1(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Menstrual headache in adolescences: Point prevalence and associated factors. (June 2017) Authors: Carman, Kursat Bora; Arslantas, Didem; Unsal, Alaettin; Atay, Emrah; Ocal, Elif Ece; Demirtas, Zeynep; Saglan, Ramazan; Yarar, Coskun; Dinleyici, Meltem Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e200 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Menstruation‐related headache in adolescents: Point prevalence and associated factors. Issue 6 (19th June 2018) Authors: Carman, Kursat Bora; Arslantas, Didem; Unsal, Alaettin; Atay, Emrah; Ocal, Ece Elif; Demirtas, Zeynep; Saglan, Ramazan; Dinleyici, Meltem; Yarar, Coskun Journal: Pediatrics international Issue: Volume 60:Issue 6(2018) Page Start: 576 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Metoclopramide-Induced Acute Dystonia: Data From a Pediatric Emergency Unit. Issue 9 (September 2021) Authors: Yarar, Coskun; Yakut, Ayten; Carman, Kursat Bora; Sahin, Sabiha; Kocak, Ozan; Ozkan, Serhat; Bal, Cengiz Journal: Pediatric emergency care Issue: Volume 37:Issue 9(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. NDE1‐related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly. Issue 1 (25th September 2021) Authors: Bas, Hasan; Saylisoy, Suzan; Cilingir, Oguz; Gokalp, Ebru Erzurumluoglu; Kocagil, Sinem; Yarar, Coskun; Aras, Beyhan Durak; Artan, Sevilhan Journal: American journal of medical genetics Issue: Volume 188:Issue 1(2022) Page Start: 326 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype. (1st May 2015) Authors: Gulec, Elif Yilmaz; Ocak, Zeynep; Candan, Sukru; Ataman, Esra; Yarar, Coskun Journal: International journal of cardiology Issue: Volume 186(2015) Page Start: 13 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗