Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Korkmaz Toygar A"'
Autor:
Simsek-Kiper, Pelin Ozlem, Kosukcu, Can, Akgun-Dogan, Ozlem, Gocmen, Rahsan, Utine, Gulen Eda, Soyer, Tutku, Korkmaz-Toygar, Ayse, Nishimura, Gen, Alikasifoglu, Mehmet, Boduroglu, Koray
Publikováno v:
In European Journal of Medical Genetics January 2019 62(1):21-26
Publikováno v:
Journal of Experimental & Clinical Medicine / Deneysel ve Klinik Tip Dergisi. Oct2022, Vol. 39 Issue 4, p1008-1012. 5p.
Publikováno v:
Güncel Pediatri. 20:289-299
Autor:
Osman Guvenc, Serdar Beken, Saygin Abali, Neslihan Yildirim Saral, Gizem Yalcin, Eda Albayrak, Burcu Bulum, Ozlem Demirelce, Serdar Basgoze, Ender Odemis, Ersin Erek, Mustafa Serteser, Ayse Korkmaz Toygar
Publikováno v:
Cardiology in the Young. 33:349-353
Background:Cyanotic CHD is a life-threatening condition that presents with low oxygen saturation in the newborn period. Hypoxemia might cause alterations in the metabolic pathways. In the present study, we aimed to evaluate the early postnatal amino
Autor:
Osman Guvenc, Serdar Beken, Aysegul Inamlik, Eda Albayrak, Bahar Temur, Serdar Basgoze, Selim Aydin, Murat Saygi, Ender Ödemiş, Ersin Erek, Ayse Korkmaz Toygar
Publikováno v:
Cardiology in the Young. 32:1644-1648
Background:The effect of prenatal diagnosis on prognosis in patients with transposition of the great arteries is not clear. In this study, we compared the outcomes after arterial switch operation.Methods:Outcome of 112 patients who had arterial switc
Autor:
Bozkaya, Davut, Korkmaz Toygar, Ayse, Turgal, Mert, Ozyuncu, Ozgur, Yigit, Sule, Yurdakok, Murat
Publikováno v:
Journal of Maternal-Fetal & Neonatal Medicine; Oct2022, Vol. 35 Issue 20, p3998-4003, 6p
Publikováno v:
The journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 35(20)
Amniotic fluid (AF) is a dynamic liquid whose contents vary according to the needs of the fetus. Levels of the amniotic components have been used in numerous studies as potential biomarkers to screen pregnancy-related abnormalities. As a reflection o
Akademický článek
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Autor:
Mehmet Alikasifoglu, Gen Nishimura, Tutku Soyer, Gülen Eda Utine, Pelin Ozlem Simsek-Kiper, Koray Boduroğlu, Can Kosukcu, Özlem Akgün-Doğan, Rahsan Gocmen, Ayse Korkmaz-Toygar
Publikováno v:
European journal of medical genetics. 62(1)
Spondylo-megaepiphyseal-metaphyseal dysplasia (SMMD) is an autosomal recessive skeletal dysplasia, characterized by disproportionate short stature with a short and stiff neck and trunk. SMMD is caused by inactivating mutations in NKX3-2, which encode
Autor:
Kartal Öztürk, Gökçen
Ülkemizde zamanında doğan yenidoğanlarda indirekt hiperbilirübinemi sıklığı oldukça yüksektir ve bu sıklık ülkemizde yapılan bilimsel çalışmalarda %20-50, fototerapi sıklığı ise %10-45 arasında bildirilmiştir. Kalıtsal metabo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10208::f47c287ef19c8de8bd6bf502c1ee4666
https://acikbilim.yok.gov.tr/handle/20.500.12812/429369
https://acikbilim.yok.gov.tr/handle/20.500.12812/429369