She was born in 1978 in Karabük. She graduated from Marmara University Faculty of Medicine in 2002. She started her specialty training in 2003 at Karadeniz Technical University Faculty of Medicine, Department of Child Health and Diseases and became a child health and disease specialist in 2009. She started her subspecialty training in 2010 at Hacettepe University Faculty of Medicine, Department of Child Neurology and became a pediatric neurology specialist in 2013. She completed her compulsory service at Giresun State Hospital between 2013-2015. She completed her master’s degree in Pediatric Neuromuscular Diseases at Hacettepe University Faculty of Medicine, Institute of Health Sciences in 2018. She started working as an academic staff at Karadeniz Technical University, Department of Child Health and Diseases, Department of Child Neurology in 2015. She currently continues to work in this staff as an Assistant Professor and is married with two children.
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More detail about the doctor
2016-2018
Mastership programme of Pediatric Neuromuscular disorders, Hacettepe University School of Medicine, Department
of Pediatric Basic Sciences, Ankara/Turkey
2014
Clinical Observer at Helsinki University Central Hospital, Department of Child
Neurology
2010-2013
Fellow of Pediatric Neurology, Hacettepe University School of Medicine, Department of Child Neurology.
Ankara/Turkey
2003-2009
Resident of Pediatri, Karadeniz Technical University School of Medicine Pediatry Department, Trabzon/Turkey
1995-2002
Marmara University, School of Medicine (English prog.), İstanbul/Turkey
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Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study
SARIKAYA UZAN G., Vural A., Yuksel D., Aksoy E., Oztoprak U., CANPOLAT M., et al.
PEDIATRIC NEUROLOGY , cilt.145, ss.3-10, 2023 (SCI-Expanded)
De novo Pure Partial Trisomy 6p Associated with Facial Dysmorphism, Developmental Delay, Brain Anomalies, and Primary Congenital Hypothyroidism
Türkyılmaz A., Cimbek E. A., Çebi A. H., Acar Arslan E., Karagüzel G.
MOLECULAR SYNDROMOLOGY , cilt.14, sa.1, ss.35-43, 2023 (SCI-Expanded)
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study
GÜNAY Ç., AYKOL D., ÖZSOY Ö., Sonmezler E., Hanci Y. S., KARA B., et al.
NEUROPEDIATRICS , cilt.54, sa.04, ss.225-238, 2022 (SCI-Expanded)
Coexistence of Spinal Muscular Atrophy Type 1 and Factor X1 Deficiency
KAYA G., BAHADIR A., ACAR ARSLAN E.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.44, sa.3, ss.115-116, 2022 (SCI-Expanded)
Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature
Ceylan A. C., Arslan E., Erdem H. B., Kavus H., Arslan M., Topaloglu H.
ACTA NEUROLOGICA BELGICA , cilt.121, sa.6, ss.1457-1462, 2021 (SCI-Expanded)
A New Case - Heterozygote PACS1 Mutation in a Patient with Schuurs-Hoeijmakers Syndrome and a Left Duplex Kidney: Case Report
Dilber B., ACAR ARSLAN E., ÇEBİ A. H., CANSU A.
HONG KONG JOURNAL OF PAEDIATRICS , cilt.26, sa.1, ss.31-33, 2021 (SCI-Expanded)
NEUROLOGICAL SYMPTOMS OF VITAMIN B12 DEFICIENCY: ANALYSIS OF PEDIATRIC PATIENTS
SERİN H. M., Arslan E.
ACTA CLINICA CROATICA , cilt.58, sa.2, ss.295-302, 2019 (SCI-Expanded)
Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders
Ceylan A. C., Citli S., Erdem H. B., Sahin I., Arslan E., Erdogan M.
MOLECULAR CYTOGENETICS , cilt.11, 2018 (SCI-Expanded)
Effect of Biperiden Treatment in Acute Orofacial and Extremity Dyskinesia With Methylphenidate Therapy
Arslan E., ARSLAN E., Kilinc A., Goksu O.
PEDIATRIC EMERGENCY CARE , cilt.34, sa.11, 2018 (SCI-Expanded)
Childhood hereditary ataxias: experience from a tertiary referral university hospital in Turkey
ARSLAN E., Gocman R., Oguz K. K., Konuskan G. D., Serdaroglu E., Topaloglu H., et al.
ACTA NEUROLOGICA BELGICA , cilt.117, sa.4, ss.857-865, 2017 (SCI-Expanded)
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