Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ayse Korkmaz Toygar"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc6b4a6abdefecddfcbbf9c66ffdd9a
https://doi.org/10.1017/s1047951122003134
https://doi.org/10.1017/s1047951122003134
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::064eed9fc68ff0ac19ad05965d951b08
https://doi.org/10.1017/s1047951121004819
https://doi.org/10.1017/s1047951121004819
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0517effa006f403a70d12f16e9756108
https://pubmed.ncbi.nlm.nih.gov/33231495
https://pubmed.ncbi.nlm.nih.gov/33231495
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::578746781bdb0f1c84d3b7f733639512
https://pubmed.ncbi.nlm.nih.gov/29704686
https://pubmed.ncbi.nlm.nih.gov/29704686