A5036366421- Epilepsy research and treatment
- Migraine and Headache Studies
- Metabolism and Genetic Disorders
- Multiple Sclerosis Research Studies
- Neonatal and fetal brain pathology
- Cerebral Venous Sinus Thrombosis
- Neurological disorders and treatments
- Pharmacological Effects and Toxicity Studies
- Hereditary Neurological Disorders
- RNA regulation and disease
- Obstructive Sleep Apnea Research
- Mitochondrial Function and Pathology
- Facial Nerve Paralysis Treatment and Research
- Obsessive-Compulsive Spectrum Disorders
- Neurological diseases and metabolism
- Cerebral Palsy and Movement Disorders
- Neuroscience and Neuropharmacology Research
- Peripheral Neuropathies and Disorders
- ATP Synthase and ATPases Research
- Cardiac Arrhythmias and Treatments
- Virology and Viral Diseases
- Autoimmune Neurological Disorders and Treatments
- Congenital Heart Disease Studies
- Pediatric Pain Management Techniques
- Congenital limb and hand anomalies
Ministry of Health
2014-2022
Memorial Ankara Hospital
2022
Akdeniz University
2019-2020
Ankara Onkoloji Eğitim ve Araştırma Hastanesi
2015-2017
Pediatrics and Genetics
2013
Childhood leukoencephalopathies are a broad class of diseases, which extremely rare. The treatment and classification these disorders both challenging. Nearly half children presenting with leukoencephalopathy remain without specific diagnosis. Leukoencephalopathy thalamus brain stem involvement high lactate (LTBL) is newly described childhood caused by mutations in the gene encoding mitochondrial aminoacyl-tRNA synthetase for glutamate, EARS2. Magnetic resonance images show characteristic...
The aim was to describe the findings on magnetic resonance imaging (MRI) in children with headache.Retrospective review of medical records patients who were admitted our pediatric outpatient neurology clinics complaint headache between January 2013 and December 2014.A total 478 (273 female, 205 male) headache. types migraine 218 (45.6%), tension-type 159 (33.3%), secondary 39 (8.2%) unspecified headaches 62 (13%) patients. Brain MRI performed 407 (85%) revealed cerebral abnormalities 128...
Episodic ataxia type 1 (EA1), a Shaker-like K+channelopathy, is consequence of genetic anomalies in the KCNA1 gene that lead to dysfunctions voltage-gated K+ channel Kv1. 1. Generally, mutations are inherited an autosomal dominant manner. Here we report clinical phenotype EA1 patient characterized by attacks decrease frequency with age, and eventually leading therapy discontinuation. A new de novo mutation (c.932G>A) changed highly conserved glycine residue into aspartate (p.G311D) was...
<b><i>Background and Aim:</i></b> Accelerated weight gain after (adeno)tonsillectomy has been reported in a number of studies. Whether is also risk factor for development overweight unknown. We investigated serum leptin plasma ghrelin levels before 1 year operation children. <b><i>Materials Methods:</i></b> studied 31 patients 29 age- sex-matched healthy control Auxologic evaluation biochemical investigations were performed surgery later....
The aim of the research is to determine etiology and clinical features seizures in critically ill children admitted a pediatric intensive care unit (PICU).
Background: Our aim in this study was to evaluate the efficacy of magnetic resonance imaging (MRI) studies detection brain regions effected by Sydenham chorea and determine whether they provided data regarding pathogenesis chorea. To end, we assessed basal ganglia structures patients control group quantitative MRI volumetric analysis. Methods: Patients with a recent onset subjects matched for age gender were included study. Medical history, laboratory tests, physical neurologic examinations...
Öz ABS
Epilepsy is the most common neurological disorder of childhood. Cognitive and behavioral changes in patients with epilepsy may be associated psychiatric disorders even these complaints purely evaluated as a disorder. In cases without clinical seizure diagnosed just symptoms. Psychiatric symptoms childhood are rarely reported literature. Epileptic psychosis involves group epileptic seizures. Interictal psychosis, postictal alternative included this group. Ictal which closely related to...
Amaç: Baş ağrısı çocuklar ve ergenlerde en sık görülen somatik yakınmadır polikliniklere başvuruların büyük bir kısmını oluşturmaktadır.Çalışmada, migren gerilim tipi baş (GTBA) tanısı konulan çocukların klinik özelliklerinin EEG bulgularının değerlendirilmesi amaçlanmıştır
Cobalamin C deficiency (CblC) is the most frequent inborn error of cobalamin (Cbl) metabolism, which has a wide clinical spectrum.Cbl defect causes accumulation methylmalonic acid and homocysteine decreased methionine synthesis.Here we presented two distinct forms patients with CblC.First patient early onset form was failure to thrive, mild hypotonia, megaloblastic anemia leukopenia at 2.5 months old.Second mental status changes, loss speech, inability walk 12 years old.Laboratory analysis...
<h3>Purpose</h3> To determine the aetiology and clinical features of seizures in critically ill children admitted to paediatric intensive care unit (PICU). <h3>Methods</h3> A total 203 were from June November 2013, 45 patients eligible. Age ranged 2 months 19 years. Seizures organised as epileptic or non-epileptic. Demographic data, PRISM III, GCS, risk factors, coexistent diagnosis, medications administered before admission, type duration seizures, drugs used, requirement mechanical...