3 results match your criteria: "Sisli Hamidiye Etfal Research Hospital[Affiliation]"

Early neurological complications in children with classical galactosemia and p.gln188arg mutation.

Int J Dev Neurosci

November 2019

Prof. Dr. Specialist in Pediatric Neurology, Department of Pediatrics, Division of Pediatric Neurology, Hacettepe University Children's Hospital, Ankara, Turkey.

Background: Despite implementation of a controlled diet, children with classical galactosemia (CG) may develop a variety of developmental and cognitive problems. In this study, we examined the early developmental status of, as well as the neurological and neuroradiological findings for, children with CG.

Methods: We retrospectively evaluated 46 galactosemia patients who were followed between 2003 and 2017.

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Aims: This study compared the early-term outcomes of mechanical ventilation (MV)/surfactant treatment with nasal-continuous positive airway pressure (nCPAP) in preterm infants with respiratory distress syndrome (RDS).

Materials And Methods: Data from newborns born between ≥24 and ≤32 weeks of gestation, hospitalized at our newborn intensive care unit, and diagnosed with RDS between January 2009 and February 2012 were analyzed.

Results: Of 193 newborns with RDS who were enrolled in the study, 113 were treated with nCPAP and 80 with MV at a level of 57.

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Background: Developed for the treatment of deformity correction, computer-assisted circular external fixators in recent years have also been used for fracture fixation. In this study, we aimed to present the efficacy of computer-assisted circular external fixator use in open long bone fractures with our new technique.

Methods: Between February 2013 and June 2014, 14 patients (mean age 24.

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