Search Results - "Olculu, Cemile Busra"
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Dysembryoplastic neuroepithelial tumors of childhood: Ege University experience
Published in Child's nervous system (01-09-2022)“…Background Dysembryoplastic neuroepithelial tumors (DNETs) are rare, low-grade tumors of the central nervous system (CNS) of childhood. It is an important…”
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Assessment of Prognostic Factors and Validity of Scoring Models in Childhood Autoimmune Encephalitis
Published in Turkish archives of pediatrics (01-03-2023)“…The aim of this study is to evaluate the prognostic factors in a single-center pediatric cohort with autoimmune encephalitis. The study group consisted of 23…”
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The Prophylaxis of Febrile Convulsions in Childhood: Secular Trends in the Last Decade (2007-2008 versus 2017-2018)
Published in The journal of pediatric research (01-03-2023)“…Aim: To analyze trends in the prophylaxis of febrile convulsions (FC) in childhood by comparing two cohorts from the previous two decades (2007-2008 versus…”
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What are the predominant predictors of seizure relapse following discontinuation of anti‐seizure medication in epileptic children?
Published in Epileptic disorders (01-04-2023)“…Objective The aim of the study was to identify the predominant predictors of seizure relapse following discontinuation of ASM in epileptic children. Methods…”
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A Rare Cause of Developmental Epileptic Encephalopathy: D-Bifunctional Protein Deficiency with a Novel Pathogenic Variant
Published in Journal of pediatric neurosciences (01-07-2023)“…A bstract Peroxisomal disorders are rare causes of severe neonatal encephalopathies. Here we report a two-month old infant with refractory neonatal seizures…”
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Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study
Published in Seizure (London, England) (01-12-2024)“…•Gene-related EO-DEEs are 48.3 % in the nationwide-Turkish cohort.•Common non-structural genetic variants are SCN1A, CDKL5, STXBP, KCNQ2, and…”
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The Utility of Genetic Testing in Infantile Epileptic Spasms Syndrome: A Step-Based Approach in the Next-Generation Sequencing Era
Published in Pediatric neurology (01-08-2024)“…To evaluate the utility of genetic testing for etiology-specific diagnosis (ESD) in infantile epileptic spasms syndrome (IESS) with a step-based diagnostic…”
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