Güncel Gönderiler: Makale Koleksiyonu
Toplam kayıt 108, listelenen: 21-40
-
A compendium answering 150 questions on COVID-19 and SARS-CoV-2
(WILEY, 2020)In December 2019, China reported the first cases of the coronavirus disease 2019 (COVID-19). This disease, caused by the severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2), has developed into a pandemic. ... -
Risk factors for severe and critically ill COVID-19 patients: A review
(WILEY, 2020)The pandemic of coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has caused an unprecedented global social and economic impact, and high numbers of deaths. ... -
Sacroiliitis in Children With Familial Mediterranean Fever
(Lippincott Williams & Wilkins, 2019)Background/Objective Familial Mediterranean fever (FMF) is an autosomal recessive disease, characterized by recurrent, self-limited attacks of fever with serositis. Various diseases were reported to be associated with FMF. ... -
Purtscher-Like Retinopathy Associated with Synthetic Cannabinoid (Bonzai) Use
(Turkish Ophthalmological Soc, 2019)Purtscher's retinopathy is a microvascular occlusive disease initially described as retinal edema, cotton wool-like exudation, and hemorrhages occurring after severe head trauma. A similar clinical presentation called ... -
Helicobacter pylori resistance to clarithromycin and fluoroquinolones in a pediatric population in Turkey: A cross-sectional study
(Wiley, 2019)BackgroundHelicobacter pylori antimicrobial resistance is gradually increasing around the world. However, there are a limited number of studies reporting on this issue in the pediatric population. In this study, we aimed ... -
Clinical and molecular characteristics and time of diagnosis of patients with classical galactosemia in an unscreened population in Turkey
(Walter De Gruyter Gmbh, 2019)Classical galactosemia is an autosomal recessive inborn error of metabolism caused by biallelic pathogenic variants in the GALT gene. With the benefit of early diagnosis by newborn screening, the acute presentation of ... -
Exposure to domestic violence and its effects on adolescents: A survey among Turkish students
(Wiley, 2019)ProblemExposure to domestic violence is an important social problem. What remains unknown are the effects of domestic violence on Turkish adolescents. MethodsThis study was performed in Krkkale, Turkey, to determine the ... -
Early neonatal outcomes of very-low-birth-weight infants in Turkey: A prospective multicenter study of the Turkish Neonatal Society
(Public Library Science, 2019)Objective To investigate the early neonatal outcomes of very-low-birth-weight (VLBW) infants discharged home from neonatal intensive care units (NICUs) in Turkey. Material and methods A prospective cohort study was performed ... -
Atypical Hemolytic Uremic Syndrome in Children Aged < 2 Years
(Karger, 2018)Background: There are limited data on infants with atypical hemolytic uremic syndrome (aHUS). The aim of this study was to determine the clinical and laboratory features, and to evaluate treatment modalities and outcomes ... -
Management of hypoglycemia in newborn: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report
(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 ... -
Incidence, risk factors and severity of retinopathy of prematurity in Turkey (TR-ROP study): a prospective, multicentre study in 69 neonatal intensive care units
(Bmj Publishing Group, 2018)Background To evaluate the prevalence, risk factors and treatment of retinopathy of prematurity (ROP) in Turkey and to establish screening criteria for this condition. Methods A prospective cohort study (TR-ROP) was performed ... -
Intracranial Lesions in Children and Adolescents with Morbid Obesity
(Galenos Yayincilik, 2017)Background: Intracranial lesions may affect the hypothalamo-hypophyseal axis and lead to some neuroendocrinological dysfunctions (hyperphagia, sleep disorders and hormonal dysfunctions). There is a very limited number of ... -
Familial Mediterranean fever-associated diseases in children
(Oxford Univ Press, 2017)Background: MEditerranean FeVer (MEFV) gene encodes for the pyrin protein and a mutated pyrin is associated with a prolonged or augmented inflammation. Hence, various diseases were reported to be associated with familial ... -
Evaluation of the functional capacity, respiratory functions and musculoskeletal systems of the children with chest pain for non-cardiac reasons
(Turkish J Pediatrics, 2017)Chronic chest pain in healthy children and adolescents generally arises from non-cardiac factors. The purpose of our study was to compare the evaluation results of effort test, respiratory function and musculoskeletal ... -
Congenital Microvillus Inclusion Disease in the Differential Diagnosis of Intractable Metabolic Acidosis
(Elsevier Taiwan, 2017)… -
Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population
(Lippincott Williams & Wilkins, 2017)Vincristine is a widely used chemotherapeutic agent in the treatment of childhood malignancies. Neuropathy is the most common adverse effect. CYP3A4 and CYP3A5 enzymes of cytochrome p450 enzyme system are responsible in ... -
Identification of three novel mutations in fourteen patients with citrullinemia type 1
(Pergamon-Elsevier Science Ltd, 2017)Objectives: Citrullinemia type 1 (CTLN1) is an autosomal recessive genetic disorder caused by mutations in the argininosuccinate synthetase 1 (ASST) gene, which encodes for the argininosuccinate synthetase enzyme. Here, ... -
First manifestation of citrullinemia type I as Sandifer syndrome
(Turkish J Pediatrics, 2017)We report an eleven-month-old infant girl who presented as Sandifer syndrome clinically but was later diagnosed with citrullinemia type I. Metabolic evaluation and molecular analysis confirmed the correct diagnosis. Despite ... -
Management of hyperbilirubinemia in preterm infants in Turkey
(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 ... -
An Assesment Of Unexpectedly High Hba1c Level In A Case With Type 1 Diabetes
(Nobel Ilac, 2016)The HbA1c test provides information about blood glucose levels of previous months depending on the erythrocyte lifetime when monitoring diabetic patients. However, various factors such as HbF and other hemoglobin variants ...