A5067588634- Epilepsy research and treatment
- Pharmacological Effects and Toxicity Studies
- Infectious Encephalopathies and Encephalitis
- Bacterial Infections and Vaccines
- Genetics and Neurodevelopmental Disorders
- Multiple Sclerosis Research Studies
- Autoimmune and Inflammatory Disorders Research
- Autism Spectrum Disorder Research
- Neurological Complications and Syndromes
- EEG and Brain-Computer Interfaces
- Viral Infections and Immunology Research
- Migraine and Headache Studies
- Genomics and Rare Diseases
- Pneumonia and Respiratory Infections
- Acute Ischemic Stroke Management
- Glycogen Storage Diseases and Myoclonus
- CNS Lymphoma Diagnosis and Treatment
- Peripheral Neuropathies and Disorders
- Cerebral Palsy and Movement Disorders
- Immune responses and vaccinations
- Infectious Diseases and Tuberculosis
- Family and Patient Care in Intensive Care Units
- Genomic variations and chromosomal abnormalities
- Fetal and Pediatric Neurological Disorders
- Cerebral Venous Sinus Thrombosis
Istanbul Medipol University
2020-2024
American Academy of Child and Adolescent Psychiatry
2022
Inonu University
2015-2021
Sağlık Bilimleri Üniversitesi
2019-2020
Kocaeli Üniversitesi
2019-2020
Turkish Armed Forces
2011-2015
Şişli Etfal Eğitim ve Araştırma Hastanesi
2011
Limb-girdle muscular dystrophy (LGMD) is the fourth most common dystrophy, with progressive proximal muscle weakness. However, a large number of neuromuscular conditions are similarly presented. Because this, use high-throughput methods such as next-generation sequencing (NGS) important in evaluation LGMD.In this report, we applied custom target capture-based NGS panel covering 31 LGMD-associated genes (MYOT, LMNA, CAV3, DES, DNAJB6, FLNC, CAPN3, DYSF, SGCG, SGCA, SGCB, SGCD, TCAP, TRIM32,...
NCs occur commonly after solid organ transplantation and affect 15%-30% of liver transplant recipients. The aim this retrospective study was to evaluate the type incidence neurologic events in pediatric patients following LT. Between May 2006 June 2015, 242 (118 females, 124 males) requiring LT for different etiologies at İnönü University Liver Transplantation Institute were included. incidence, types, risk factors that occurred evaluated retrospectively. Neurologic 57 (23.5%) patients....
Vitamin D deficiency and insufficiency are related with many neurological diseases such as migraine. The aim of this study was to investigate whether pediatric migraine is associated vitamin the effect therapy on frequency, duration, severity attacks, Pediatric Migraine Disability Assessment (PedMIDAS).We retrospectively examined patients' levels calcium, phosphorus, parathyroid hormone, alkaline phosphatase, 25-OH 92 patients. patients were divided into two groups: Group 1, which had low...
Abstract Background Many studies evaluating the nutritional status of children with cerebral palsy (CP) have focused on energy requirements and protein intake. The present work aimed to assess micronutrient levels (CP). Methods This multicenter, cross‐sectional observational study was conducted in 10 different cities Turkey. Data were available for 398 participants. Anthropometric measurements, feeding mode, status, evaluated. Results participants (303 patients 95 healthy controls)....
Febrile seizures are the most common seizure type of childhood, and prognosis is usually good. Many factors that increase risk recurrence develop epilepsy have been identified. This study aims to determine clinical characteristics patients who were admitted with febrile seizure, outcomes treatment, factors.Between January 2017 2019, 147 (42.6%) female 198 (57.4%) male aged between 3-60 months included in study.The mean age at time admission was 30.4±15.4 months, first 21.2±12.8 months....
Kılıç B, Güngör S, Özgör B. Clinical, electrophysiological findings and evaluation of prognosis patients with Guillain-Barré syndrome. Turk J Pediatr 2019; 61: 200-208. syndrome (GBS) is an acute inflammatory polyneuropathy characterized by frequent rapid progressive, ascending, symmetric weakness areflexia. We aimed to evaluate the etiology, clinical treatment GBS in our clinic. Patients who were diagnosed clinic between 2009 2017 evaluated retrospectively. The study included 20 female 25...
Abstract Background We aimed to examine suicide probability, factors affecting suicide, and personality traits of children adolescents diagnosed with epilepsy, compare their results those without epilepsy. Methods Fifty‐six epilepsy 56 control children, aged 11–16 years, were evaluated by using the Diagnostic Statistical Manual Mental Disorders diagnostic criteria, Kiddie Schedule for Affective Schizophrenia Present Lifetime Version, Child Depression Inventory, Suicide Probability Scale...
Mutations in mammalian membrane-bound O-acyltransferase domain-containing (MBOAT) 7 gene are a rare cause for intellectual disability, developmental delay, autistic findings, epilepsy, truncal hypotonia with appendicular hypertonia, and below-average head sizes. Pathogenic variants MBOAT7 show these nonspecific clinical features that seen many other neurometabolic diseases. Therefore, specific neuroimaging findings can be valuable key factors differential diagnosis. Magnetic resonance...
The aim of this study was to evaluate the risk factors, clinical implications, and prognosis new-onset seizures that occurred after pediatric liver transplantation, assess efficacy levetiracetam treatment. laboratory data transplanted 28 children who had transplantation specifically 18 received were analyzed retrospectively. Sixteen patients (88.9%) remained seizure-free in 2 (11.1%), more than 50% reduction detected with In conclusion, are generally most common complication by a spectrum...