Travaux scientifiques

Prof. Dr. Sarenur Gökben

155 publications. La source de l’information est indiquée à côté de chaque publication.

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  1. Optical genome mapping identifies previously undetected causal variants in early-onset developmental epileptic encephalopathies

    Journal of Medical Genetics, 2026

    DOI 10.1136/jmg-2026-111485 PMID 41991279 Source : OpenAlex

  2. Efficacy and Safety Study of the Revised Ege Pediatric Status Epilepticus Protocol (r-EPSEP)

    Journal of Child Neurology, 2025

    DOI 10.1177/08830738251346214 PMID 40525484 1 citation (Europe PMC) Source : OpenAlex

  3. The Role of Diffusion Tensor Magnetic Resonance Imaging in Understanding Neurological and Ocular Outcomes in Preterm Infants with Periventricular Leukomalacia

    Forbes Journal of Medicine, 2025

    DOI 10.4274/forbes.galenos.2025.94940 Texte intégral en libre accèsSource : OpenAlex

  4. The Utility of Genetic Testing in Infantile Epileptic Spasms Syndrome: A Step-Based Approach in the Next-Generation Sequencing Era

    Pediatric Neurology, 2024

    DOI 10.1016/j.pediatrneurol.2024.05.018 PMID 38905742 4 citations (Europe PMC) Source : OpenAlex

  5. Canpolat, Temel Pediatrik Epilepsi

    Akademisyen Kitabevi eBooks, 2024

    DOI 10.37609/akya.3122 Texte intégral en libre accèsSource : OpenAlex

  6. Yenidoğan Dönemi Konvülziyonları ve Epilepsileri

    Akademisyen Kitabevi eBooks, 2024

    DOI 10.37609/akya.3122.c12197 Source : OpenAlex

  7. Kumandaş & Canpolat Pediatrik ve Neonatal EEG Atlası

    Akademisyen Kitabevi eBooks, 2023

    DOI 10.37609/akya.2036 Texte intégral en libre accèsSource : OpenAlex

  8. What are the predominant predictors of seizure relapse following discontinuation of anti‐seizure medication in epileptic children?

    Epileptic Disorders, 2023

    DOI 10.1002/epd2.20019 PMID 37358927 4 citations (Europe PMC) Source : OpenAlex

  9. Assessment of Prognostic Factors and Validity of Scoring Models in Childhood Autoimmune Encephalitis

    Turkish Archives of Pediatrics, 2023

    DOI 10.5152/turkarchpediatr.2023.22198 PMID 36856351 Texte intégral en libre accèsSource : OpenAlex

  10. Sleep problems in adolescents with epilepsy and their caregivers: associations with behavioural difficulties

    The Turkish Journal of Pediatrics, 2023

    DOI 10.24953/turkjped.2022.56 PMID 37395969 7 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  11. Developmental Epileptic Encephalopathies in A National Cohort Study (Turkish EPISTEP -1): A Step-based Approachment for Etiologic Diagnosis

    Kocaeli Üniversitesi - AVESİS, 2022

    Source : OpenAlex

  12. Continuous EEG Monitoring in Critically Ill Children and Prognostic Factors for Short-term Outcome: An Observational Study

    The Journal of Pediatric Research, 2022

    DOI 10.4274/jpr.galenos.2022.77885 Texte intégral en libre accèsSource : OpenAlex

  13. Pediatrik Nöroloji: Algoritmalar ve İlaç Rehberi

    Akademisyen Kitabevi eBooks, 2022

    DOI 10.37609/akya.2035 Texte intégral en libre accèsSource : OpenAlex

  14. Cerebral folate transporter deficiency: a potentially treatable neurometabolic disorder

    Acta Neurologica Belgica, 2021

    DOI 10.1007/s13760-021-01700-7 PMID 34002331 12 citations (Europe PMC) Source : OpenAlex

  15. Cerebral sinovenous thrombosis in children: A single-center experience

    Turkish Archives of Pediatrics, 2021

    DOI 10.5152/turkarchpediatr.2021.20073 PMID 34104915 3 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  16. Two Concomitant Cases with Febrile Infection-Related Epilepsy Syndrome (FIRES) treated with andldquo;3-Dimensional Combination Treatment Protocolandrdquo;

    journal of Clinical Case Reports, 2021

    DOI 10.37421/2165-7920.2021.11.1407 Source : OpenAlex

  17. Melatonin Versus Chloral Hydrate for Sleep Electroencephalography Recording in Children: A Comparative Study Using Bispectral Index Monitoring Scores and Electroencephalographic Sleep Stages

    Journal of Clinical Neurophysiology, 2021

    DOI 10.1097/wnp.0000000000000829 PMID 33606431 7 citations (OpenAlex) Source : OpenAlex

  18. Serebral Palside Erken Tanı ve Ayırıcı Tanı

    2021

    Source : OpenAlex

  19. Efficacy of levetiracetam as first-line therapy for neonatal clinical seizures and neurodevelopmental outcome at 12 months of age

    Acta Neurologica Belgica, 2020

    DOI 10.1007/s13760-020-01366-7 PMID 32424740 5 citations (Europe PMC) Source : OpenAlex

  20. Sulthiame add-on treatment in children with epileptic encephalopathy with status epilepticus: an efficacy analysis in etiologic subgroups

    Neurological Sciences, 2020

    DOI 10.1007/s10072-020-04526-y PMID 32592101 7 citations (Europe PMC) Source : OpenAlex

  21. Clinical spectrum, treatment and outcome of myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease in children: a tertiary care experience

    Acta Neurologica Belgica, 2020

    DOI 10.1007/s13760-020-01499-9 PMID 33231843 6 citations (Europe PMC) Source : OpenAlex

  22. Neuropsychological outcome in cases with acute disseminated encephalomyelitis

    The Turkish Journal of Pediatrics, 2020

    DOI 10.24953/turkjped.2020.04.009 PMID 32779412 5 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  23. CSF levels of a set of neurotrophic factors (brain-derived neurotrophic factor, nerve growth factor) and neuropeptides (neuropeptide Y, galanin) in epileptic children

    Journal of Clinical Neuroscience, 2020

    DOI 10.1016/j.jocn.2020.04.064 PMID 32327377 4 citations (Europe PMC) Source : OpenAlex

  24. Dirençli Epilepsinin Tedavi Edilebilir Bir Nedeni: Piridoksin Bağımlı Epilepsi

    Turkish Journal of Pediatric Disease, 2020

    DOI 10.12956/tchd.568456 Texte intégral en libre accèsSource : OpenAlex

  25. Kalıtsal Metabolik Epilepsiler

    2020

    Source : OpenAlex

  26. A transcranial magnetic stimulation study for the investigation of corticospinal motor pathways in children with cerebral palsy

    Journal of Clinical Neuroscience, 2020

    DOI 10.1016/j.jocn.2020.04.087 PMID 32334959 16 citations (OpenAlex) Source : OpenAlex

  27. Dropped head related lamin A/C associated congenital muscular dystrophy case; previously defined as emerydreifuss muscular dystrophy

    The Turkish Journal of Pediatrics, 2020

    DOI 10.24953/turkjped.2020.01.019 PMID 32253878 5 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  28. The utility of whole exome sequencing for identification of the molecular etiology in autosomal recessive developmental and epileptic encephalopathies

    Neurological Sciences, 2020

    DOI 10.1007/s10072-020-04619-8 PMID 32705489 8 citations (OpenAlex) Source : OpenAlex

  29. The histopathologic examination of a second muscle biopsy specimen at a later date may sometimes be the best approach to make a differential diagnosis in neuromuscular disorders

    Turkish Journal of Pathology, 2020

    DOI 10.5146/tjpath.2019.01512 PMID 33432556 3 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  30. A rare case of peripheral nerve hyperexcitability in childhood: Isaacs syndrome

    Journal of Pediatric Neurosciences, 2020

    DOI 10.4103/jpn.jpn_128_19 PMID 33042252 7 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  31. Pediatrik non-travmatik koma prognozunu öngörmede klinik, elektroensefalografik ve nöroradyolojik parametrelerin rolü

    Pamukkale Medical Journal, 2020

    DOI 10.31362/patd.685215 4 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  32. A rare cause of ischemic stroke in childhood: spontaneous long segment intracranial dissection

    Child s Nervous System, 2020

    DOI 10.1007/s00381-020-04530-9 PMID 32034519 4 citations (OpenAlex) Source : OpenAlex

  33. Necessity of Electroencephalography in High-risk Brief Resolved Unexplained Event

    The Journal of Pediatric Research, 2019

    DOI 10.4274/jpr.galenos.2019.80958 7 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  34. Hereditary Neuropathy with Liability to Pressure Palsy: A Case Diagnosed with a Quick Multiplex Ligation-dependent Probe Amplification Test

    The Journal of Pediatric Research, 2019

    DOI 10.4274/jpr.galenos.2018.60590 Texte intégral en libre accèsSource : OpenAlex

  35. Acquired Demyelinating Syndrome: Single Center Experience

    Journal of Dr Behcet Uz Children s Hospital, 2019

    DOI 10.5222/buchd.2019.59023 Texte intégral en libre accèsSource : OpenAlex

  36. X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients

    Scientific Reports, 2019

    DOI 10.1038/s41598-019-48385-w PMID 31427717 23 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  37. The case of pyridoxine dependent epilepsy misdiagnosed as non-ketotic hyperglycinemia

    The Turkish Journal of Pediatrics, 2019

    DOI 10.24953/turkjped.2019.04.019 PMID 31990480 8 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  38. De Novo CHRNE Mutation: Congenital Myasthenic Syndrome

    The Journal of Pediatric Research, 2019

    DOI 10.4274/jpr.galenos.2019.77045 2 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  39. Akut Ensefalopatide Elektroensefalografi Bulguları

    Turkiye Klinikleri Pediatric Sciences - Special Topics, 2019

    Source : OpenAlex

  40. ELECTROENCEPHALOGRAPHY FINDINGS IN ACUTE ENCEPHALOPATHY

    Turkiye Klinikleri eBooks, 2019

    DOI 10.5336/978-605-7650-49-8_p147 Source : OpenAlex

  41. WWOX-associated encephalopathies: identification of the phenotypic spectrum and the resulting genotype-phenotype correlation

    Neurological Sciences, 2018

    DOI 10.1007/s10072-018-3528-6 PMID 30094525 12 citations (Europe PMC) Source : OpenAlex

  42. Determining Risk Factors of Epilepsy in Children with Cerebral Palsy: A Retrospective Study

    The Journal of Pediatric Research, 2018

    DOI 10.4274/jpr.24471 11 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  43. A rare casue of brachial plexopathy: hereditary neuralgic amyotrophy

    Türk Pediatri Arşivi, 2018

    DOI 10.5152/turkpediatriars.2018.5837 PMID 31619932 5 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  44. Intracranial Hypertension in Children: Etiological, Clinical Features, Treatment and Prognosis

    Turkiye Klinikleri Journal of Pediatrics, 2018

    DOI 10.5336/pediatr.2018-61528 1 citation (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  45. WWOX related epileptic encephalopathy: A new autosomal recessively inherited disorder.

    Kocaeli Üniversitesi - AVESİS, 2018

    Source : OpenAlex

  46. Prevalence and severity of malnutrition in pediatric neurology outpatients with respect to underlying diagnosis and comorbid nutrition and feeding related problems

    The Turkish Journal of Pediatrics, 2018

    DOI 10.24953/turkjped.2018.06.012 PMID 31365208 12 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  47. Sturge-Weber Syndrome Type III

    The Journal of Pediatric Research, 2018

    DOI 10.4274/jpr.44265 2 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  48. Extreme delta brush activity; could it be a marker for early diagnosis and prognosis of anti- NMDA encephalitis?

    Türk Pediatri Arşivi, 2018

    DOI 10.5152/turkpediatriars.2018.4628 PMID 31217713 3 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  49. Akut Güçsüzlük ve Motor Kayıp ile Başvuran Çocuğa Yaklaşım

    Turkiye Klinikleri Pediatric Sciences - Special Topics, 2018

    Source : OpenAlex

  50. Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database

    European Journal of Paediatric Neurology, 2017

    DOI 10.1016/j.ejpn.2017.06.004 PMID 28694135 23 citations (Europe PMC) Source : OpenAlex