A5077366174- Epilepsy research and treatment
- Neonatal and fetal brain pathology
- Metabolism and Genetic Disorders
- Multiple Sclerosis Research Studies
- Genetics and Neurodevelopmental Disorders
- Pharmacological Effects and Toxicity Studies
- Peripheral Neuropathies and Disorders
- EEG and Brain-Computer Interfaces
- Cerebral Palsy and Movement Disorders
- Diet and metabolism studies
- Infectious Encephalopathies and Encephalitis
- Neurogenetic and Muscular Disorders Research
- Neurological disorders and treatments
- Genomics and Rare Diseases
- Hereditary Neurological Disorders
- Neuroscience and Neuropharmacology Research
- Genetic Neurodegenerative Diseases
- Neonatal Respiratory Health Research
- Ocular Diseases and Behçet’s Syndrome
- Neurological diseases and metabolism
- Burkholderia infections and melioidosis
- Neuroscience of respiration and sleep
- Autoimmune and Inflammatory Disorders
- Child Nutrition and Feeding Issues
- Neurological and metabolic disorders
Ege University
2016-2025
Dicle University
2024
Uniwersytecki Szpital Dziecięcy
2023
Children's Clinical University Hospital
2023
Izmir University
2020
Ege Üniversitesi Tıp Fakültesi Hastanesi
2018-2020
Pediatrics and Genetics
2020
Child Neurology Associates
2020
University of Rochester Medical Center
2019
Dr. Behçet Uz Çocuk Hastalıkları Hastanesi
2017
Electrical status epilepticus in slow wave sleep (ESES) is a rare, age-related, self-limited disorder characterized as epilepsy with different seizure types, neuropsychological impairment the form of global or selective regression cognitive functions, motor impairment, and typical electroencephalographic (EEG) findings continuous epileptic activity occupying 85% nonrapid eye movement sleep.The aim to examine clinical electrophysiological treatment modalities children ESES evaluate outcome...
Despite being a treatable and preventable zoonosis, brucellosis is still endemic in certain areas of the world. Nervous system involvement rare but an important complication childhood. Neurobrucellosis should be taken into consideration differential diagnosis any kind neurological signs, particularly areas. The authors present patient with neurobrucellosis who presented isolated intracranial hypertension without other systemic symptoms brucellosis.
The objective of this study is to evaluate neurologic problems caused by nutritional vitamin B12 deficiency in infancy. Twenty-four cases between 2 and 18 months age with symptoms and/or signs diagnosed as were analyzed. most common developmental retardation, afebrile seizures, involuntary movements. mean levels lower patients both extraneurologic involvement when compared those only symptoms. All the treated B12. In severe deficiencies, movements observed during treatment using...
Multiple sclerosis is an uncommon disease in childhood and adolescence rarely associated with movement disorders other than tremor. The differential diagnosis difficult to establish when, particularly, disorder presents as the initial manifestation of multiple sclerosis. Video-electroencephalography monitoring gold-standard method for epileptic paroxysmal nonepileptic events, including psychogenic seizures. This article a patient dystonia secondary who previously was diagnosed treated having...
Hereditary lower motor neuron diseases (LMND) other than 5q-spinal muscular atrophy (5q-SMA) can be classified according to affected muscle groups. Proximal and distal forms of non-5q-SMA represent a clinically genetically heterogeneous spectrum characterized by significant overlaps with axonal Charcot-Marie-Tooth (CMT) disease. A consensus for the best approach molecular diagnosis needs reached, especially in light continuous novel gene discovery falling costs next-generation sequencing...