| Epilepsy in neurofibromatosis type 1: Diffuse cerebral dysfunction? E Serdaroglu, B Konuskan, KK Oguz, G Gurler, D Yalnizoglu, B Anlar Epilepsy & Behavior 98, 6-9, 2019 | 30 | 2019 |
| Expanding the phenotype of phospholipid remodelling disease due to MBOAT7 gene defect D Yalnızoǧlu, RK Özgül, KK Oǧuz, B Özer, D Yücel‐Yılmaz, B Gürbüz, ... Journal of Inherited Metabolic Disease 42 (2), 381-388, 2019 | 22 | 2019 |
| Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span D Yücel-Yılmaz, E Yücesan, D Yalnızoğlu, KK Oğuz, MŞ Sağıroğlu, ... Brain and Development 40 (6), 458-464, 2018 | 14 | 2018 |
| Cobalamin C disease missed by newborn screening in a patient with low carnitine level RC Ahrens-Nicklas, E Serdaroglu, C Muraresku, C Ficicioglu JIMD Reports, Volume 23, 71-75, 2015 | 14 | 2015 |
| Autoimmune epilepsy and/or limbic encephalitis can lead to changes in sleep spindles E Serdaroğlu, FI Tezer, S Saygi Archives of neuropsychiatry 55 (4), 320, 2018 | 12 | 2018 |
| Parental perception and child's nutritional status S YALÇIN, E Serdaroglu, O Ince Turkish Journal of Pediatrics 58 (1), 2016 | 10 | 2016 |
| Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype YK Terzi, B Sirin, G Hosgor, E Serdaroglu, B Anlar, S Aysun, S Ayter Child's Nervous System 28, 943-946, 2012 | 9 | 2012 |
| A Turkish BCS1L mutation causes GRACILE-like disorder B Serdaroglu, S Takci, H Kotarsky, O Çil, G Utine, Ş Yiğit, V Fellman Turkish Journal of Pediatrics 58 (6), 2016 | 8 | 2016 |
| Access to Pediatric Neurology training and services worldwide: A survey by the International Child Neurology Association JM Wilmshurst, C Catsman-Berrevoets, DL Gilbert, L Nagarajan, P Samia, ... Neurology 101 (18), 798-808, 2023 | 6 | 2023 |
| Maternal Germline Mosaicism of a de Novo TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings Ş Çitli, E Serdaroglu Fetal and pediatric pathology 41 (1), 155-165, 2022 | 4 | 2022 |
| Screening traumatic life events in preschool aged children: cultural adaptation of Child and Adolescent Trauma Screen (CATS) Caregiver-report 3-6 years version P Akkuş, E Serdaroğlu, A Kömürlüoğlu, M Asena, E Bahadur, G Özdemir, ... Turkish Journal of Pediatrics 63 (1), 2021 | 4 | 2021 |
| COVID-19 and Neurological Manifestations E Serdaroğlu, A Serdaroğlu Türkiye Klinikleri. Tip Bilimleri Dergisi 40 (2), 269-271, 2020 | 4 | 2020 |
| Childhood hereditary ataxias: experience from a tertiary referral university hospital in Turkey EA Arslan, R Göçmen, KK Oğuz, GD Konuşkan, E Serdaroğlu, ... Acta Neurologica Belgica 117, 857-865, 2017 | 4 | 2017 |
| Absence of exon 17 c. 2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype YK Terzi, B Sirin, E Serdaroglu, B Anlar, S Aysun, G Hosgor, EA Arslan, ... Child's Nervous System 27, 2113-2116, 2011 | 4 | 2011 |
| İntrauterin testis torsiyonu: Bir vaka takdimi E Serdaroğlu, Ş Takcı, R User, Ş Güçer, Ş Yiğit, M Yurdakök Çocuk Sağlığı ve Hastalıkları Dergisi 54, 223-6, 2011 | 4 | 2011 |
| Broadening the clinical spectrum: molecular mechanisms and new phenotypes of ANO3-dystonia J Ousingsawat, K Talbi, H Gómez-Martín, A Koy, A Fernández-Jaén, ... Brain, awad412, 2023 | 3 | 2023 |
| Trends in the choice of antiseizure medications in juvenile myoclonic epilepsy: A retrospective multi-center study from Turkey between 2010 and 2020 B Kılıç, E Serdaroğlu, BG Polat, T İnce, G Esenülkü, Y Topçu, ... Seizure 99, 48-53, 2022 | 3 | 2022 |
| Is There a Tendency for Autoimmunity in Neurofibromatosis Type 1? S Esra, G Ceren, S Erdal, B Hatice, E Fatma, A Banu Indian journal of pediatrics 89 (5), 510-512, 2022 | 3 | 2022 |
| A t (5; 16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delay A Ozantürk, EE Davis, A Sabo, MM Weiss, D Muzny, S Dugan-Perez, ... Molecular Case Studies 2 (2), a000703, 2016 | 3 | 2016 |
| Etiological yield of muscle biopsy in the newborn period E Serdaroglu, G Haliloglu, B Talim, S Yigit, M Yurdakok, H Topaloğlu Neuromuscular Disorders 25, S286, 2015 | 2 | 2015 |
