Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Rüya Çolak"'
Autor:
Ezgi Yangın Ergon, Rüya Çolak, Demet Terek, Özge Altun Köroğlu, Şebnem Çalkavur, Nilgün Kültürsay
Publikováno v:
Journal of Pediatric Research, Vol 11, Iss 2, Pp 80-87 (2024)
Aim: According to delivery room guidelines, an optimal position is not specified for the stabilization of the baby. This study aimed to define the positions effects on postnatal adaptation parameters and cerebral oxygenation in non-resuscitated neona
Externí odkaz:
https://doaj.org/article/7ae047dfd05d40c8935edd1a083dff8a
Autor:
Rüya ÇOLAK, Meltem KIVILCIM, Senem ALKAN ÖZDEMİR, Ezgi YANGIN ERGON, Sebnem ÇALKAVUR, Tülin GÖKMEN YILDIRIM
Publikováno v:
Forbes Tıp Dergisi, Vol 3, Iss 3, Pp 297-302 (2022)
Objective: Today, the survival rate of low-birth-weight infants has increased thanks to supportive care. However, various permanent health problems, especially neurodevelopmental retardation, can be seen in these infants. This study investigates the
Externí odkaz:
https://doaj.org/article/41f43408f8634b829d2f5caa7c0fec87
Autor:
Mehmet Coşkun, Oğuz Han Kalkanlı, Rüya Çolak, Senem Alkan Özdemir, Tülin Gökmen Yıldırım, Şebnem Çalkavur, Fazıl Gelal
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 11, Iss 1, Pp 15-22 (2021)
Objective: The aim of this study is to compare magnetic resonance imaging (MRI) findings with severity of hypoxic-ischemic encephalopathy (HIE) in term neonates. Methods: Sixty-three newborns with HIE in whom cranial MRIs were performed within the fi
Externí odkaz:
https://doaj.org/article/8cb13c25f78145f6a56e0a807955d83f
Autor:
Rüya Çolak, Şebnem Çalkavur, Ezgi Yangın Ergon, Kıymet Çelik, Senem Alkan Özdemir, Özgür Olukman, Zeynep Üstünyurt
Publikováno v:
Journal of Pediatric Research, Vol 7, Iss 2, Pp 152-157 (2020)
Aim:Neonatal bilirubin-induced neurologic dysfunction can present with a wide spectrum of symptoms from mild neurologic impairment to severe acute bilirubin encephalopathy. In this study, we aimed to determine the risk factors of unconjugated hyperbi
Externí odkaz:
https://doaj.org/article/562d5dbea864410bba2beda898eaa8eb
Autor:
Rüya Çolak, Ezgi Yangın Ergon, Senem Alkan Özdemir, Ferit Kulalı, Meral Yıldız, Oğuzhan Kalkanlı, Tülin Gökmen Yıldırım, Şebnem Çalkavur
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 3, Pp 245-248 (2019)
Introduction: Although drug poisoning rarely occurs during the neonatal period,morbidity and mortality are high when it occurs.Two cases who were admitted to the Emergency Department of our hospital due to digoxin and phenobarbital poisoning with a t
Externí odkaz:
https://doaj.org/article/1b371c26175c4ee49d130acf76935100
Autor:
Ferit Kulalı, Melis Köse, Tuğçe Candan Çelik, Ezgi Yangın Ergon, Oğuz Han Kalkanlı, Rüya Çolak, Meral Yıldız, Senem Alkan Özdemir, Tülin Gökmen Yıldırım, Şebnem Çalkavur
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 2, Pp 143-148 (2019)
INTRODUCTION: The deficiency or absence of an enzyme or cofactor in the metabolic pathway leads to the formation or accumulation of a specific metabolite resulting in inborn errors of metabolism (IEM).The neonate who is, usually, born healthy at birt
Externí odkaz:
https://doaj.org/article/2d3cf77c07b54f45b089d09de1b20adb
Autor:
Ezgi Yangın Ergon, Senem Alkan Özdemir, Rüya Çolak, Kıymet Çelik, Özgür Olukman, Şebnem Çalkavur
Publikováno v:
Journal of Pediatric Research, Vol 4, Iss 4, Pp 249-252 (2017)
Hemolysis and jaundice related to Rh incompatibility in the neonatal period has decreased substantially due to the widespread use of anti-D gammaglobulin in recent years. Nevertheless, the rate of subgroup mismatch in the etiology of hemolytic diseas
Externí odkaz:
https://doaj.org/article/d40c9f0120064b2dbb6d9f167506fe0d
Publikováno v:
Balkan Medical Journal, Vol 34, Iss 6, Pp 580-583 (2017)
Background: Glucose transporter type 1 deficiency syndrome is the result of impaired glucose transport into the brain. Patients with glucose transporter type 1 syndrome may present with infantile seizures, developmental delay, acquired microcephaly,
Externí odkaz:
https://doaj.org/article/e025eb567fa44549b7b5ecc493d4d7e5
Autor:
Cüneyt Zihni, Murat Muhtar Yılmazer, Senem Alkan Özdemir, Rüya Çolak, Ferit Kulali, Oguz Han Kalkanli, Şebnem Çalkavur, Tulin Gokmen Yildirim, Ezgi Yangın Ergon
Publikováno v:
Gynecology Obstetrics & Reproductive Medicine. 27:175-180
Objective: Hemodynamically significant patent ductus arteriosus(hsPDA) is resulting in severe mortality and morbidity in infants with extremely low birth weight(ELBW). In our study, we aimed to evaluate the necessity of performing routine echocardiog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ada852041b5451fe2227ba3f40817c8
https://doi.org/10.21613/gorm.2021.1168
https://doi.org/10.21613/gorm.2021.1168
Publikováno v:
Molecular Syndromology. 12:269-278
Craniofrontonasal syndrome (CFNS) is a rare X-linked genetic disorder which is characterized by coronal synostosis, widely spaced eyes, a central nasal groove, and various skeletal anomalies. Mutations in the EFNB1 gene in Xq13.1 are responsible for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a010a073fc1bc8156de9082a43e5fa30
https://doi.org/10.1159/000515697
https://doi.org/10.1159/000515697