Sevim Ünal
6 Papers
4 Citations
Sevim Ünal is an academic researcher. The author has contributed to research in topics: Neonatal intensive care unit & Gene. The author has an hindex of 3, co-authored 6 publications.
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Papers
•Journal Article
Outcomes of very low birth weight infants in a newborn tertiary center in Turkey, 1997-2000.
TL;DR: It was prospectively shown that 111 of the surviving infants could be regularly followed in a newborn follow-up clinic to provide health maintenance, developmental assessment and support and compared with reports from other developing countries, VLBW infants at this center had higher survival rates.
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Anne Sütü İle Beslenen Bir Yenidoğan Hipernatremik Dehidratasyon
Begüm Atasay,Ayla Günlemez,Sevim Ünal,Saadet Arsan +3 more
- 01 Jan 2003
TL;DR: Otuzbes yasindaki annenin sorunsuz gebeligini takiben dogan ilk bebegi, on gunlukken malnutrisyon ve hipernatremik dehidratasyon tanisiyla yenidogan yogunbakim unitesine yatirildi, tekrar anne sutu ile beslenmeye baslanilamadi.
Clinical importance of neonatal autopsies
Halil Özdemir,Begüm Atasay,Ayla Günlemez,Aylin Okçu Heper,Sevim Ünal,Saadet Arsan +5 more
- 01 Jan 2005
TL;DR: Clinicians can confidently advise parents of the usefulness of the neonatal autopsy in ascertaining the cause of death or for counseling their future pregnancy.
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Clinical importance of neonatal autopsies Yenidoğan otopsilerinin klinik önemi
Halil Özdemir,Begüm Atasay,Ayla Günlemez,Aylin Okçu Heper,Sevim Ünal,Saadet Arsan +5 more
- 01 Feb 2005
TL;DR: In this paper, Yenidogan et al. presented the results of a study at the Turkish University of Ankara's Faculty of Medicine and stated that the results showed that 95% of the participants in the study were male.
Congenital early onset isolated adrenocorticotropin deficiency associated with a TPIT gene mutation.
Begüm Atasay,Zehra Aycan,Evliyaoğlu O,Pelin Adiyaman,Ayla Günlemez,Sevim Ünal,Saadet Arsan,Gönül Öcal,Merih Berberoğlu +8 more
TL;DR: A neonate is presented with the diagnosis of congenital early onset isolated ACTH deficiency (IAD) associated with a loss of POMC function as a result of a missense mutation in the TPIT gene.