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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.
Ozantürk A, Marshall JD, Collin GB, Düzenli S, Marshall RP, Candan Ş, Tos T, Esen İ, Taşkesen M, Çayır A, Öztürk Ş, Üstün İ, Ataman E, Karaca E, Özdemir TR, Erol İ, Eroğlu FK, Torun D, Parıltay E, Yılmaz-Güleç E, Karaca E, Atabek ME, Elçioğlu N, Satman İ, Möller C, Muller J, Naggert JK, Özgül RK. Ozantürk A, et al. Among authors: cayir a. J Hum Genet. 2015 Jan;60(1):51. doi: 10.1038/jhg.2014.101. J Hum Genet. 2015. PMID: 25619591 No abstract available.
Cushing's syndrome due to topical steroid.
Cayir A, Kaya A, Davutoğlu S, Küçükaslan I, Ozkan B. Cayir A, et al. West Indian Med J. 2013 Jan;62(1):104-5. West Indian Med J. 2013. PMID: 24171340 No abstract available.
An investigation of the effect of thiamine pyrophosphate on cisplatin-induced oxidative stress and DNA damage in rat brain tissue compared with thiamine: thiamine and thiamine pyrophosphate effects on cisplatin neurotoxicity.
Turan MI, Cayir A, Cetin N, Suleyman H, Siltelioglu Turan I, Tan H. Turan MI, et al. Among authors: cayir a. Hum Exp Toxicol. 2014 Jan;33(1):14-21. doi: 10.1177/0960327113485251. Epub 2013 Apr 30. Hum Exp Toxicol. 2014. PMID: 23632005
RECURRENT RAB3GAP1 MUTATIONS IN THE TURKISH POPULATION.
Tasdemir S, Sahin I, Morris-Rosendahl DJ, Marzioglu E, Cayir A, Yuce I, Tatar A. Tasdemir S, et al. Among authors: cayir a. Genet Couns. 2015;26(4):415-23. Genet Couns. 2015. PMID: 26852512
Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience.
Esen İ, Bayramoğlu E, Yıldız M, Aydın M, Karakılıç Özturhan E, Aycan Z, Bolu S, Önal H, Kör Y, Ökdemir D, Ünal E, Önder A, Evliyaoğlu O, Çayır A, Taştan M, Yüksel A, Kılınç A, Büyükinan M, Özcabı B, Akın O, Binay Ç, Kılınç S, Yıldırım R, Aytaç EH, Sağsak E. Esen İ, et al. Among authors: cayir a. J Clin Res Pediatr Endocrinol. 2019 May 28;11(2):164-172. doi: 10.4274/jcrpe.galenos.2018.2018.0210. Epub 2018 Nov 29. J Clin Res Pediatr Endocrinol. 2019. PMID: 30488822 Free PMC article.
Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study.
Akıncı A, Türkkahraman D, Tekedereli İ, Özer L, Evren B, Şahin İ, Kalkan T, Çürek Y, Çamtosun E, Döğer E, Bideci A, Güven A, Eren E, Sangün Ö, Çayır A, Bilir P, Törel Ergür A, Ercan O. Akıncı A, et al. Among authors: cayir a. J Clin Res Pediatr Endocrinol. 2019 Nov 22;11(4):341-349. doi: 10.4274/jcrpe.galenos.2019.2019.0021. Epub 2019 Apr 17. J Clin Res Pediatr Endocrinol. 2019. PMID: 30991789 Free PMC article.
122 results