Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Ferit Kulali"'
Autor:
Ezgi Yangın Ergon, Ruya Colak, Meltem Kıvılcım, Meral Yıldız, Senem Alkan Özdemir, Ferit Kulali, Sebnem Calkavur
Publikováno v:
Forbes Tıp Dergisi, Vol 1, Iss 3, Pp 68-74 (2020)
INTRODUCTION: Prophylactic caffeine therapy, reduces the frequency of apnea in premature babies. Moreover, its effect has been well established in reducing the intermittent hypoxemia, and the need for additional ventilator support of infants with a b
Externí odkaz:
https://doaj.org/article/0c730690ab644ffdbbf6a1d03e55cf6c
Autor:
Sebnem Calkavur, Senem Alkan Ozdemir, Ruya Colak, Ezgi Yangin Ergon, Ferit Kulali, Tulin Gokmen Yildirim
Publikováno v:
Gynecology Obstetrics & Reproductive Medicine, Vol 26, Iss 1, Pp 64-69 (2020)
OBJECTIVE: We aimed to investigate the role of incomplete of antenatal steroid therapy by comparing with no and complete steroid exposure on mortality and morbidity in preterm infants. STUDY DESIGN: This is a prospective, an observational study whic
Externí odkaz:
https://doaj.org/article/03ce4a8713444252bcc4df5df4f64f2a
Autor:
Ferit Kulali, Ahmet Yagmur Bas, Fatma Iyigun Guzel, Husniye Yucel, Caner Kara, Cigdem Uner, Nihal Demirel
Publikováno v:
Journal of the Pakistan Medical Association, Vol 71, Iss 3 (2020)
Published in March 2021
Externí odkaz:
https://doaj.org/article/4f0b2bc894d344f4841d2c365a146507
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
Autor:
Ahmet Yagmur Bas, Fatma Iyigun Guzel, Husniye Yucel, Caner Kara, Cigdem Uner, Nihal Demirel, Ferit Kulali
Publikováno v:
Journal of the Pakistan Medical Association. :1-7
Papillorenal syndrome, also known as renal coloboma syndrome, is characterised by congenital optic disc anomalies and renal abnormalities. Mutations in the PAX2 gene, which plays a critical role in embryogenesis, cause this syndrome. Other related an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::915622eed8d5ff0f971a51cf2ce51db7
https://doi.org/10.47391/jpma.1158
https://doi.org/10.47391/jpma.1158
Autor:
Ferit Kulali, Beyza Ozcan, Sezin Unal, Husniye Yucel, Nihal Demirel, Ahmet Yagmur Bas, Dilek Ulubas Isik
Publikováno v:
Journal of Pediatric Infectious Diseases. 14:223-227
Objective Health care associated infections (HAIs) in the neonatal intensive care unit (NICU) are a significant cause of neonatal morbidity and mortality. Enterobacter aerogenes, a gram-negative bacterium, rarely causes HAI in the pediatric and NICUs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47a5b0336f6b1f4918e9d1a2a81d2b7d
https://doi.org/10.1055/s-0039-1691780
https://doi.org/10.1055/s-0039-1691780
Autor:
Orkan Ergün, Ferit Kulali, Burak Polat, Senem Alkan-Ozdemir, Cigden Omur-Ecevit, Nebahat Ermis, Ezgi Yangın-Ergon, Meral Yildiz, Rüya Çolak, Şebnem Çalkavur
Publikováno v:
Euroasian Journal of Hepato-Gastroenterology
Introduction Abernethy malformation is a very rare condition in which mesenteric venous blood is drained into systemic circulation by an extra hepatic portosystemic shunt. Here we present a case of a female in infantile period who is a liver transpla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52b9963eaf02505c93ca34edd6f55af4
https://doi.org/10.5005/jp-journals-10018-1283
https://doi.org/10.5005/jp-journals-10018-1283
Autor:
Canan Aygün, Esin Koç, M. Yekta Öncel, Mehmet Satar, Belma Saygili Karagol, Salih Çağrı Çakır, Kadir Şerafettin Tekgündüz, Nejat Narli, Sezin Unal, Yalçın Çelik, Saime Sündüz Uygun, Adil Umut Zübarioğlu, Nükhet Aladağ Çiftdemir, Demet Terek, Ayşe Ecevit, Ibrahim Murat Hirfanoglu, Emel Okulu, Didem Aliefendioğlu, Ozge Saglam, Sule Yigit, Hasan Tezer, Ayşegül Zenciroğlu, Ali Bulbul, Serdar Beken, Münevver Türkmen, Esra Onal, Nuran Üstün, Nihal Oygür, Asuman Coban, Ferit Kulali, Tugba Gursoy, Sevim Ünal, Tuğba Bedir Demirdağ, Adviye Çakıl Sağlık, Suna Oguz, Fatma Narter
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 2, Pp 208-217 (2021)
Pediatrics and Neonatology
Pediatrics and Neonatology
Background: healthcare-acquired infections (HAIs) in the neonatal period cause substantial morbidity, mortality, and healthcare costs. Our purpose was to determine the prevalence of HAIs, antimicrobial susceptibility of causative agents, and the adap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad9c7d788d0de7af2a29790a018f36aa
https://hdl.handle.net/11454/69587
https://hdl.handle.net/11454/69587
Autor:
Rüya Çolak, Meltem Kıvılcım, Şebnem Çalkavur, Senem Alkan Özdemir, Meral Yildiz, Ezgi Yangın Ergon, Ferit Kulali
Publikováno v:
Forbes Journal of Medicine.
INTRODUCTION: Prophylactic caffeine therapy, reduces the frequency of apnea in premature babies. Moreover, its effect has been well established in reducing the intermittent hypoxemia, and the need for additional ventilator support of infants with a b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::140782d1965e4f065fa7849d4c49932a
https://doi.org/10.5222/forbes.2020.57441
https://doi.org/10.5222/forbes.2020.57441
Autor:
Ezgi Yangın Ergon, Rüya Çolak, Melis Köse, Taner Atilgan, Erkin Serdaroglu, Meral Yildiz, Ferit Kulali, Fatma Aslan, Garry K. Brown, Ruth M. Brown, Şebnem Çalkavur, Senem Alkan
Pyruvate carboxylase (PC) deficiency is a rare autosomal recessive disease and provides clinics in three essential phenotypes. Type B PC deficiency is characterized by lactic acidosis and hyperammonemia. We report a Turkish patient who was diagnosed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22f60e18fc5ff2d19a2cb0ce1c5d8c74
https://hdl.handle.net/11499/37203
https://hdl.handle.net/11499/37203