452 results match your criteria: "İzmir Dr. Behcet Uz Children's Hospital[Affiliation]"
Psychiatr Danub
December 2021
University of Health Sciences, Dr. Behcet Uz Children's Hospital, Pediatric Intensive Care Unit, Ismet Kaptan Neighborhood, Sezer Doğan Street, 11, 35210, Izmir, Turkey,
Background: Coronavirus disease 2019 (COVID-19) may affect the mental status of health care professionals. The purpose of our study is to evaluate the mental health effects of the COVID-19 epidemic on health care professionals in the pediatric intensive care units (PICUs).
Subjects And Methods: Our study was conducted prospectively between 01.
Nephrol Dial Transplant
November 2022
Department of Nephrology, Radboud University Medical Center, Nijmegen, The Netherlands.
Turk Arch Pediatr
September 2021
Pediatric Palliative Care Center, Dr. Behçet Uz Children's Hospital, Izmir, Turkey.
Objective: Pediatric palliative care is a top-level care system that focuses on improving the quality of life of the child and family. Quality of life is an expression of individual well-being based on an individual's assessment of their own life. It includes satisfaction in all areas of life, including physical and mental health, environment, and social areas.
View Article and Find Full Text PDFArch Pediatr
February 2022
Department of Pediatric Intensive Care, Dr. Behcet Uz Children's Hospital, Konak, Izmir 35210, Turkey.
Objective: The aim of this study was to determine the association between the use of intravenous N-acetylcysteine (NAC) and hepatic healing in pediatric intensive care unit (PICU) patients with non-acetaminophen-induced hepatic injury, except for acute liver failure.
Methods: The data of patients who received intravenous NAC as adjuvant therapy for transaminase levels more than sixfold normal values during their PICU stay between 2010 and 2014 were retrospectively collected from the medical records database. The patients who did not receive NAC with elevated transaminase levels during their PICU stay between 2014 and 2018 were also collected as the standard of care (SOC) cohort.
J Trop Pediatr
December 2021
Department of Paediatric Infectious Diseases, University of Health Sciences Dr. Behçet Uz Children's Hospital, İzmir 35210, Turkey.
Objectives: This descriptive study aimed to compare the clinical and laboratory features of the children with the multisystem inflammatory syndrome in children (MIS-C), requiring pediatric intensive care unit (PICU), admission with the MIS-C patients who did not require PICU admission.
Patients And Methods: This study was conducted between March 2020 and February 2021 at the University of Health Sciences Dr. Behçet Uz Children's Hospital, a referral center for pediatric infectious diseases in the Aegean Region of Turkey.
Obesity (Silver Spring)
December 2021
Department of Neurology, University of Michigan, Ann Arbor, Michigan, USA.
Objective: The aim of this study was to determine the effect of dietary weight loss on neuropathy outcomes in people with severe obesity.
Methods: A prospective cohort study of participants attending a medical weight-management program was followed. Weight loss was achieved with meal replacement of 800 kcal/d for 12 weeks and then transitioning to 1,200 to 1,500 kcal/d.
Presse Med
November 2021
Division of Endocrinology and Metabolism, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey. Electronic address:
Lipodystrophy syndromes are rare complex multisystem disorders caused by generalized or partial lack of adipose tissue. Adipose tissue dysfunction in lipodystrophy is associated with leptin deficiency. Lipodystrophy leads to severe metabolic problems.
View Article and Find Full Text PDFEpileptic Disord
December 2021
Department of Medical Biology and Genetics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.
Homozygous OCLN variants have been reported in patients with band-like calcification with simplified gyration and polymicrogyria (BLC-PMG) which is characterized by microcephaly, intracranial calcification and severe developmental delay. The OCLN gene encodes the integral membrane protein, occludin. Herein, we report three additional cases with homozygous OCLN variants that were identified via Trio-WES in two consanguineous unrelated families.
View Article and Find Full Text PDFInt J Clin Pract
December 2021
Department of Pediatric Emergency, Dr. Behçet Uz Children's Hospital, University of Health Sciences, Izmir, Turkey.
Hum Vaccin Immunother
November 2021
Division of Infectious Disease, Department of Pediatrics, Medical School of Ege University, Izmir, Turkey.
Varicella is a vaccine-preventable disease, and the incidence of varicella has declined since the introduction of varicella vaccine campaigns. A wild type of varicella zoster virus (VZV) was isolated from a 33-month-old child with varicella in Korea in 1989, a different strain (MAV/06). A live-attenuated varicella vaccine containing strain (MAV/06), Suduvax®, was developed in South Korea in 1994.
View Article and Find Full Text PDFAnatol J Cardiol
October 2021
Department Of Pediatric Cardiology, Dr. Behcet Uz Children's Hospital, Izmir, Turkey.
Mol Syndromol
August 2021
Department of Neonatology, Dr. Behcet Uz Children's Hospital, Izmir, Turkey.
Craniofrontonasal syndrome (CFNS) is a rare X-linked genetic disorder which is characterized by coronal synostosis, widely spaced eyes, a central nasal groove, and various skeletal anomalies. Mutations in the gene in Xq13.1 are responsible for familial and sporadic cases.
View Article and Find Full Text PDFRheumatol Int
March 2022
Pediatric Rheumatology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Heart Surg Forum
July 2021
University of Health Sciences Izmir Dr. Behcet Uz Children's Hospital, Department of Pediatric Cardiac Surgery, Izmir, Turkey.
Objectives: Cardioplegia solutions have a role not only in arresting the heart but also in protecting the myocardium from ischemia. While antegrade cardioplegia is given by the heart-lung machine in many centers, it is given by a hand-squeezed bag in very few centers. The pressure of cardioplegia given antegrade from the heart-lung machine is certain (60-90 mmHg).
View Article and Find Full Text PDFJ Pediatr Urol
October 2021
Dr. Behçet Uz Children's Hospital, Izmir, Turkey. Electronic address:
J Clin Endocrinol Metab
January 2022
Department of Pediatric Endocrinology and Diabetes, Marmara University, School of Medicine, Istanbul, Turkey.
Background: Aldosterone synthase deficiency (ASD) caused by mutations in the CYP11B2 gene is characterized by isolated mineralocorticoid deficiency. Data are scarce regarding clinical and biochemical outcomes of the disease in the follow-up.
Objective: Assessment of the growth and steroid profiles of patients with ASD at the time of diagnosis and after discontinuation of treatment.
Turk J Pediatr
August 2021
Department of Pediatrics, Health Sciences University, Dr. Behcet Uz Children's Hospital, İzmir, Turkey.
Background: Functional gastrointestinal disorders (FGID) may affect or may be affected by postpartum depression (PPD), mode of feeding and postpartum life quality. We aimed to evaluate the interaction between FGID and these parameters in infants.
Methods: The study group consisted of babies attending our outpatient clinics.
J Pediatr Hematol Oncol
March 2022
Department of Pediatric Nephrology, Dr. Behçet Uz Children's Hospital, İzmir, Turkey.
Background: Hypertension (HTN) is a complication of pediatric hematopoietic stem cell transplantation. We report a pediatric stem cell transplant patient who had HTN and adverse event because of amlodipine.
Observation: Seven-year-old boy had haploidentical stem cell transplantation with post-transplant cyclophosphamide.
Am J Infect Control
September 2021
Department of Paediatric Infectious Diseases, University of Health Sciences Dr. Behçet Uz Children's Hospital, İzmir, Turkey.
Background: The study aimed to evaluate the distribution of circulating respiratory viral pathogens other than severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) during the first year of the coronavirus disease-2019 (COVID-19) pandemic with especially focusing on the effects of the national-based mitigation strategies.
Methods: This single-center study was conducted between March 11, 2020-March 11, 2021. All children who were tested by polymerase chain reaction on nasopharyngeal swabs for SARS-CoV-2 and other common respiratory viral pathogens were included in the study.
J Clin Immunol
August 2021
Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Background: Inborn errors of immunity (IEIs) are a heterogeneous group of genetic defects of immunity, which cause high rates of morbidity and mortality mainly among children due to infectious and non-infectious complications. The IEI burden has been critically underestimated in countries from middle- and low-income regions and the majority of patients with IEI in these regions lack a molecular diagnosis.
Methods: We analyzed the clinical, immunologic, and genetic data of IEI patients from 22 countries in the Middle East and North Africa (MENA) region.
J Pediatr Nurs
December 2021
Ege University Faculty of Nursing, Department of Pediatric Nursing, Turkey.
Purpose: Even the healthiest neonates experience pain during painful interventions (e.g. administration of Vitamin K, heel lance) in their first moments of life.
View Article and Find Full Text PDFJCI Insight
May 2021
Department of Neurology, University of Michigan, Ann Arbor, Michigan, USA.
BACKGROUNDWe aimed to determine whether metabolic syndrome (MetS) affects longitudinal trajectories of diabetic complications, including neuropathy, cardiovascular autonomic neuropathy (CAN), and kidney disease in American Indians with type 2 diabetes.METHODSWe performed a prospective study where participants underwent annual metabolic phenotyping and outcome measurements. The updated National Cholesterol Education Program criteria were used to define MetS and its individual components, using BMI instead of waist circumference.
View Article and Find Full Text PDFPediatr Infect Dis J
July 2021
Department of Pediatric Infectious Diseases and Department of Radiology, Dr. Behçet Uz Children's Hospital, İzmir, Turkey.
Blood Coagul Fibrinolysis
June 2021
Department of Pediatric Hematology.
Patients with haemophilia A who have similar FVIII levels show clinical heterogeneity, and 10-15% of patients with severe haemophilia do not have a severe bleeding phenotype. The aim of this study was to assess whether global haemostasis tests, such as thrombin generation assay (TGA) and thromboelastography (TEG), can predict the bleeding pattern of severe haemophilia better than trough levels and pharmacokinetic profiles, particularly in the prophylactic setting. The study group consisted of 39 patients with haemophilia A and 75 healthy controls.
View Article and Find Full Text PDFTurk J Pediatr
August 2021
Department of Pediatric Infectious Diseases, University of Health Sciences Dr. Behçet Uz Children's Hospital, İzmir, Turkey.
Background: The increasing prevalence of methicillin-resistant Staphylococcus aureus (MRSA) and its resistance to multiple antibiotics has become a serious challenge since the early 2000s. Especially, community-acquired MRSA (CA-MRSA) infections that appear mainly as skin and soft tissue infections (SSTIs) tend to increase worldwide. The objective of this cross-sectional study was to evaluate the trends in the frequency of SSTIs due to community-acquired S.
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