A5085270334- Fetal and Pediatric Neurological Disorders
- Neonatal and fetal brain pathology
- Epilepsy research and treatment
- Metabolism and Genetic Disorders
- Migraine and Headache Studies
- Cerebrospinal fluid and hydrocephalus
- Glioma Diagnosis and Treatment
- Sleep and related disorders
- Infectious Encephalopathies and Encephalitis
- Attention Deficit Hyperactivity Disorder
- Mitochondrial Function and Pathology
- Spinal Dysraphism and Malformations
- Neurological disorders and treatments
- Advanced MRI Techniques and Applications
- Neuroblastoma Research and Treatments
- Neurosurgical Procedures and Complications
- Genomics and Rare Diseases
- Sleep and Wakefulness Research
- Diet and metabolism studies
- EEG and Brain-Computer Interfaces
- Genetic Neurodegenerative Diseases
- Genetics and Neurodevelopmental Disorders
- Traumatic Brain Injury and Neurovascular Disturbances
- Advanced Neuroimaging Techniques and Applications
- Neuroscience of respiration and sleep
Kent Hastanesi
2021-2025
Acıbadem Adana Hospital
2021-2025
Acıbadem University
2012-2021
Kocaeli Üniversitesi
2020
Seoul School of Integrated Sciences and Technologies
2012
Marmara University
1999-2009
Institute of Neurological Sciences
2008
University of North Carolina at Chapel Hill
2001-2002
Child Neurology Associates
2002
Communities In Schools of Orange County
2002
Abstract To evaluate the efficacy of specific sublingual immunotherapy (SLIT), we enrolled 15 children with asthma and rhinitis (7 girls, 8 boys,mean ± SD age 11.7 3.3) allergic to house dust mite (HDM) into a double‐blind, placebo‐controlled study. After run‐in period, patients were randomized receive either placebo (n = 7) or SLIT 8) standardized Dermatophagoides pteronyssinus ( D. ) + farinea 50/50 extract. They received increasing doses up 100 index units reactivity (IR) every day for 4...
We aimed to understand the genetic etiology in children presenting with epilepsy and/or developmental delay by using next-generation sequencing (NGS). included our pediatric neurology clinic a diagnosis of between January 2019 and December 2021. evaluated patients NGS equipment laboratory. In total, 90 were study. Twenty (34.4%) out 58 who had undergone whole-exome (WES) pathogenic or likely (P/LP) variants 11 (18.9%) unknown significance (VUS). Five (41.6%) 12 whole-genome P/LP 5 VUS....
In this population-based study, we aimed to determine the total sleep duration (TSD), its association with socio-economic status (SES) and behavioural symptoms among schoolchildren.A cross-sectional study was performed schoolchildren in Istanbul. A structured questionnaire evaluating schedule variables filled out by their parents. SES determined according Turkish scale.The mean age of 2669 children 8.2 ± 2.4 years, 51% students were girls. The TSD 10.20 1.04, bedtime 21.57 0.56 (both hours,...
The etiology and pathogenesis of migraine other types headache are still under discussion. An interaction organic, psychological, psychosocial factors is operative. In this study, we aimed to determine the prevalence its association with socioeconomic status among schoolchildren.A cross-sectional study was performed on 2669 schoolchildren via a parental questionnaire. Socioeconomic determined according Turkish scale.The mean age students 8.2 +/- 2.4 years. 46.2% (95% CI: 44.3-48.1). 3.4%...
Introduction Rare and ultra-rare genetic conditions significantly contribute to infant morbidity mortality, often presenting with atypical features heterogeneity that complicate management. Rapid genome sequencing (RGS) offers a timely cost-effective approach diagnosis, aiding in early clinical management reducing unnecessary interventions. This pilot study represents the inaugural use of next-generation (NGS) as diagnostic instrument for critically ill neonatal pediatric ICU patients...
The aim of this study was to determine electrocardiographic changes in children during seizures.We assessed heart rate changes, RR intervals and QT 47 seizures children. Consecutive were measured for 60 s before the seizures, after video electroencephalography monitoring.There 18 patients. Five patients had generalized 13 focal seizures. Twelve male. mean age monitoring 10.1 years (range 4 months-19 years). Ictal tachycardia seen every seizure. No ictal bradycardia noted. There only one...
Abstract Background GLUT1 Deficiency Syndrome 1 (GLUT1DS1) is a neurological disorder caused by either heterozygous or homozygous mutations in the Solute Carrier Family 2, Member ( SLC2A1 ) gene. encodes Glucose transporter type (GLUT1) protein, which primary glucose at blood–brain barrier. A ketogenic diet (KD) provides an alternative fuel for brain metabolism to treat impaired transport. By reanalyzing exome data, we identified de novo variant girl with epilepsy. After reversed phenotyping...