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Esra Serdaroglu
Esra Serdaroglu
M.D. , Ph.D.
Verified email at hacettepe.edu.tr - Homepage
Title
Cited by
Cited by
Year
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
282019
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
222019
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
142015
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
132018
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
122018
Parental perception and child's nutritional status
S YALÇIN, E Serdaroglu, O Ince
Turkish Journal of Pediatrics 58 (1), 2016
102016
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
92012
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
82016
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
42023
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
42022
COVID-19 and Neurological Manifestations
E Serdaroğlu, A Serdaroğlu
Türkiye Klinikleri. Tip Bilimleri Dergisi 40 (2), 269-271, 2020
42020
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
42017
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
42011
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
42011
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
32016
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
22022
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
22021
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
22015
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
12023
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
12022
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