Yazar "Aliefendioglu, Didem" için listeleme
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Anesthesia for a child with Walker-Warburg syndrome
Kose, Emine Arzu; Bakar, Bulent; Ates, Gokay; Aliefendioglu, Didem; Apan, Alpaslan (Elsevier Science Inc, 2014)Background and objectives: Walker-Warburg Syndrome is a rare, autosomal recessive con-genital muscular dystrophy manifested by central nervous system, eye malformations andpossible multisystem involvement. The diagnosis ... -
Breast-feeding-associated hypernatremia: Retrospective analysis of 169 term newborns
Unal, Sevim; Arhan, Ebru; Kara, Nazli; Uncu, Nermin; Aliefendioglu, Didem (Wiley, 2008)Background: The aim of the present paper was to define the incidence, complications, morbidity and mortality of hypernatremic dehydration due to inadequate breast-feeding in a neonatal intensive care unit. Methods: A ... -
Can cerebrospinal fluid uric acid levels differentiate intraventricular hemorrhage from traumatic tap?
Aliefendioglu, Didem; Gürsoy, Tuğba; Hayran, K. Mutlu; Aslan, Ayşe Tana (Karger, 2006)Objective: To measure blood and cerebrospinal fluid (CSF) uric acid (UA) levels of neonates with intraventricular hemorrhage (IVH), and to examine whether or not UA can be used to differentiate traumatic tap from IVH. ... -
Can Resistin be a New Indicator of Neonatal Sepsis?
Aliefendioglu, Didem; Gursoy, Tugba; Caglayan, Osman; Aktas, Alev; Ovali, Fahri (Elsevier Taiwan, 2014)Background: Sepsis is an important cause of neonatal death and perinatal brain damage, particularly in preterm infants. It is thought that activation of the inflammatory cascade triggered by cytokine might play a role in ... -
Cerebral MRI findings in neonatal hypoglycemia
Metabolic disturbances such as anoxia and hypoglycemia may adversely alter the development of the neonatal brain. While rapid and appropriate diagnosis with adequate therapy has a good prognosis; delayed detection and/or ... -
Could Lower Bone Turnover be a Cause of Chest Pain During Childhood?
Şanli, Cihat; Akalın, Nursel; Koçak, Ülker; Erol, Reyhan; Albayrak, Meryem; Aliefendioglu, Didem; Hizel, Selda (Springer, 2010)Chest pain, a frequent complaint during childhood, rarely originates from a cardiac pathology. Although it usually is idiopathic, it also could be associated with psychogenic, musculoskeletal, respiratory, and digestive ... -
Do cerebral blood flow velocities change in iron deficiency anemia?
Aliefendioglu, Didem; Yilmaz, Sevda; Misirlioglu, Emine Dibek; Saygi, Semra; Özdoğan, Selver; Koçak, Ülker (Lippincott Williams & Wilkins, 2007)Infants with iron deficiency had lower scores when tested for mental and motor development than their peers with better iron status. The aim of this study was to examine cerebral blood flow velocity in infants with iron ... -
Effect of phototherapy on gastrointestinal smooth muscle activity and oxidative stress
Soyer, Tutku; Aliefendioglu, Didem; Aktuna, Zuhal; Caglayan, Osman; Aydos, Tolga Resat; Cakmak, Murat (Springer, 2011)Aim To evaluate the effect of phototherapy on gastrointestinal smooth muscle activity and oxidative stress. Methods Wistar albino rats (n = 18, in the first 7 days of life) weighing 7 +/- 2 g with both sexes were included ... -
Effect of phototherapy on growth factor levels in neonatal rat skin
Soyer, Tutku; Ayva, Sebnem; Aliefendioglu, Didem; Aktuna, Zuhal; Aslan, Mustafa Kemal; Senyucel, Mine Fedakar; Cakmak, Murat (W B Saunders Co-Elsevier Inc, 2011)Aim: Neonates undergoing surgery may receive phototherapy (PT) for the treatment of hyperbilirubinemia. Although the effects of PT on neonatal structures are well documented, the effect of PT on wound healing has not been ... -
Haemorrhagic pneumonia caused by Stenotrophomonas maltophilia in two newborns
Guzoglu, Nilufer; Demirkol, Fatma N.; Aliefendioglu, Didem (J Infection Developing Countries, 2015)Invasive procedures and antibiotic treatment increase the risk of nosocomial infections in neonatal intensive care units. Early identification and appropriate treatment is important. Herein we report two cases of massive ... -
Heart Rate Variability in Neonates with Hypoxic Ischemic Encephalopathy
Aliefendioglu, Didem; Dogru, Tolga; Albayrak, Meryem; DibekMisirlioglu, Emine; Sanli, Cihat (All India Inst Medical Sciences, 2012)Objective To evaluate the changes in heart rate variability (HRV) in newborns with hypoxic-ischemic encephalopathy (HIE). Methods Twenty-two newborns (14 boys, 8 girls) with moderate or severe HIE and 24 term neonates with ... -
Management of hyperbilirubinemia in preterm infants in Turkey
Guzoglu, Nilufer; Tandircioglu, Umit Ayse; Aliefendioglu, Didem (Tubitak Scientific & Technical Research Council Turkey, 2016)Background/aim: Prematurity is a significant risk factor for developing unconjugated hyperbilirubinemia. This study investigated the current approach to managing hyperbilirubinemia in preterm newborns in Turkey. Materials ... -
Management of hypoglycemia in newborn: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report
Aliefendioglu, Didem; Coban, Asuman; Hatipoglu, Nihal; Ecevit, Ayse; Arisoy, Ayse Engin; Yesiltepe, Gul; Ozek, Eren (Turkish Pediatrics Assoc, 2018)Hypoglycemia is one of the most important and most common metabolic problems of the newborn because it poses a risk of neurological injury, if it is prolonged and recurs. Therefore, newborns who carry a risk of hypoglycemia ... -
A newborn with VLCAD deficiency Clinical, biochemical, and histopathological findings
Aliefendioglu, Didem; Dursun, Ali; Coskun, Turgay; Akcoeren, Zuhal; Wanders, Ronald J. A.; Waterham, Hans R. (Springer, 2007)Here we report a newborn with VLCAD deficiency with a severe neonatal onset type who presented with hypoglycemia, cardiomyopathy, mild hepatomegaly and slight hypoalbuminemia. The patient was also homozygous for a new ... -
A novel mutation which causes a frameshift in thePHOX2Bgene causes Haddad syndrome
Guzoglu, Nilufer; Aslan, Mustafa K.; Gunay, Yasemin D.; Atasoy, Pinar; Ceylaner, Serdar; Aliefendioglu, Didem (LIPPINCOTT WILLIAMS & WILKINS, 2020)[Özet Yok] -
Novel Mutations in the PC Gene in Patients with Type B Pyruvate Carboxylase Deficiency
Ostergaard, Elsebet; Duno, Morten; Moller, Lisbeth Birk; Kalkanoglu-Sivri, H. Serap; Dursun, Ali; Aliefendioglu, Didem; Wibrand, Flemming (Springer-Verlag Berlin, 2013)We have investigated seven patients with the type B form of pyruvate carboxylase (PC) deficiency. Mutation analysis revealed eight mutations, all novel. In a patient with exon skipping on cDNA analysis, we identified a ...