Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Meltem Bor"'
Publikováno v:
ENT Updates, Vol 14, Iss 1, Pp 15-18 (2024)
Externí odkaz:
https://doaj.org/article/f335a5cb47794a139c4065e0cf08c6ae
Autor:
Özkan İlhan, Senem Alkan Özdemir, Sinem Akbay, Berat Kanar, Şeyma Memur, Meltem Bor, Esra Arun Özer
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 3, Pp 175-182 (2019)
INTRODUCTION: To determine whether non-synchronized nasal intermittent positive pressure ventilation (NIPPV) reduces extubation failure, compared to nasal continuous positive airway pressure (NCPAP), in preterm infants with respiratory distress syndr
Externí odkaz:
https://doaj.org/article/6354316a25154f0a8d393f8043d278a6
Publikováno v:
Balkan Medical Journal, Vol 28, Iss 02, Pp 219-221 (2011)
Dandy-Walker variant (DWV) might be considered as one of the borderlines in the examination of fetal brain. We report the first case of a DWV in a fetus conceived by ICSI. A 34 year-old woman underwent assisted reproductive treatment due to male fact
Externí odkaz:
https://doaj.org/article/8c3628e1fc6a43cc99e12861dcec9ebd
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 03, Pp 243-244 (2011)
Externí odkaz:
https://doaj.org/article/e3818388401d4b03a903951ddacb9935
Publikováno v:
Klinische Padiatrie.
Publikováno v:
Klinische Padiatrie. 234(4)
This study aimed to assess the risk factors for clinical seizures in newborns treated with whole body cooling (WBC) for hypoxic ischemic encephalopathy (HIE).Infants with gestational age≥36 weeks and birth weight≥2.000 g who were treated with WBC
Publikováno v:
J Pediatr Intensive Care
Pompe disease (PD) is an autosomal recessive lysosomal storage disorder caused by a deficiency of acid α-1,4-glucosidase enzyme (GAA). PD has two forms, namely the infantile-onset and the late-onset form. In untreated cases, infantile-onset form usu
Publikováno v:
J Pediatr Intensive Care
Pseudohypoaldosteronism is a rare disease characterized by resistance to aldosterone-targeted organs, hyponatremia, hyperkalemia, metabolic acidosis, and severe salt loss in hyperaldosteronism. Homozygous mutations in SCNN1A, SCNN1B, and SCNN1G genes
Autor:
Meltem Bor, Ali Rahmi Bakiler, Sinem Akbay, Senem Alkan Özdemir, Ozkan Ilhan, Berat Kanar, Şeyma Memur, Esra Arun Özer
Publikováno v:
Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi. 17:342-344
Aim: The purpose of this study is to compare the clinical criteria of preterm infants on their third day of life with their echocardiographic findings for the correct diagnosis of hemodynamically significant patent ductus arteriosus (hsPDA). Material
Autor:
Meltem Bor, Ozkan Ilhan
Publikováno v:
Pediatrics International. 61:697-705
Platelet mass index (PMI) is associated with platelet functionality. The aim of this study was to evaluate the role of PMI in predicting the severity of transient tachypnea of the newborn (TTN).Infants with gestational age ≥37 weeks and birthweight