A5087601774- Glioma Diagnosis and Treatment
- Cerebrospinal fluid and hydrocephalus
- Epilepsy research and treatment
- Spinal Dysraphism and Malformations
- Head and Neck Surgical Oncology
- Meningioma and schwannoma management
- Vascular Malformations Diagnosis and Treatment
- Fetal and Pediatric Neurological Disorders
- Spinal Fractures and Fixation Techniques
- Intracranial Aneurysms: Treatment and Complications
- Traumatic Brain Injury and Neurovascular Disturbances
- Spine and Intervertebral Disc Pathology
- Neuroblastoma Research and Treatments
- Pharmacological Effects and Toxicity Studies
- Teratomas and Epidermoid Cysts
- Neurofibromatosis and Schwannoma Cases
- Brain Metastases and Treatment
- Neuroscience and Neuropharmacology Research
- Scoliosis diagnosis and treatment
- Neonatal and fetal brain pathology
- Metabolism and Genetic Disorders
- Bone Tumor Diagnosis and Treatments
- Hedgehog Signaling Pathway Studies
- EEG and Brain-Computer Interfaces
- Craniofacial Disorders and Treatments
Istanbul Medipol University
2017-2024
Hacettepe University
2011-2022
University of California, Los Angeles
2016
Boğaziçi University
2016
Charles University
2015
Acıbadem University
2015
Past Global Changes
2009
Turkish Thoracic Society
2007
Neurology, Inc
2006
Hacettepe University Hospital
1997-2006
Slow-growing, low-grade temporal lobe tumors are one of the most common causes epilepsy in children. Although there numerous consistent features this patient group, consensus about management and surgical approach is lacking. In study authors review clinical, pathological, radiological as well outcome data obtained 29 pediatric patients with tumor-related discuss treatment strategies.In who presented intractable seizures secondary to mass lesions underwent comprehensive workup, tumor was...
✓ A patient is described who had a solitary left frontal intracranial chondroma originating from the falx cerebri. The tumor was totally removed. diagnostic value of computerized tomography and surgical findings in this rare pathological condition are discussed.
L-2-Hydroxyglutaric aciduria (L-2-HGA, MIM 236792) is a rare autosomal recessive neurodegenerative disorder characterized by psychomotor delay, cerebellar and extrapyramidal signs subcortical leukoencephalopathy with basal ganglia dentate nuclei involvement. Mutations in the gene L2HGDH (C14orf160/duranin/) have been identified as causative for L-2-HGA. A feature disproportionally associated L-2-HGA development of malignant brain tumors. In our cohort 40 patients L-2-HGA, two developed...
Abstract Background Posterior fossa syndrome (PFS) is defined as the temporary and complete loss of speech after posterior surgery. The goal this study was to identify incidence risk factors for PFS determine accompanying neurobehavioral psychologic problems. Procedure Between May 2007 April 2009, children with brain tumors having surgery were evaluated neurologically psychologically in preoperative postoperative period. Results developed 9 patients among 36 (25%) included study. Mutism...
Instrumentation and correction of severe congenital scoliosis, particularly in patients with spinal dysraphism, has been reported to cause a high potential rate neurological compromise after instrumentation. The aim this study was evaluate the safety efficacy posterior instrumentation scoliosis accompanying dysraphism.Level IV therapeutic studies.Retrospective x-ray measurements analyze evaluation hospital charts document intraoperative postoperative complications were performed for...
To evaluate the clinical characteristics and long-term outcome of pediatric patients with optic glioma.A total 101 glioma newly diagnosed between 1975 2008 were evaluated retrospectively. COPP (cyclophosphamide, vincristine, procarbazine, prednisolone) cisplatin plus etoposide most commonly used chemotherapy regimens. Radiotherapy was administered in progressive or unresponsive disease.The median age at time diagnosis 6 years, male/female ratio 1.15. The common referral complaint strabismus....