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의료진 소개

최선아 의사

최선아 교수


소아청소년과, 극희귀질환센터 관심의료진 등록

전문 진료 분야

소아신경, 뇌전증, 경련, 두통, 발달장애, 신경근육질환 ※ 단기연수 (25.3/1~25.8/31)

진료 일정

학력 및 경력사항

학력사항

  • 서울대학교 의과대학 박사
  • 서울대학교 의과대학 석사
  • 서울대학교 의과대학 졸업

교육 및 연구경력

  • 2023-현재  | 이대목동병원 소아청소년과 임상부교수
  • 2020-2023  | 이대목동병원 소아청소년과 임상조교수
  • 2019-2020  | 단국대학교병원 소아청소년과 임상조교수
  • 2017-2019  | 분당서울대학교병원 소아청소년과 진료교수
  • 2015-2017  | 서울대학교병원 소아청소년과 임상강사
  • 2011-2015  | 서울대학교병원 소아청소년과 전공의
  • 2010-2011  | 서울대학교병원 인턴

수상경력

  • 2021 | 대한소아신경학회 최우수 논문상
  • 국제뇌전증학회 우수 초록상 (Best Abstract Contribution, 32nd International Epilepsy Congress, Barcelona, Spain)

기타 학술 관련 경력

  • 대한소아청소년과학회 정회원 (청소년위원회 위원)
  • 대한소아신경학회 정회원 (홍보정보위원회, 기획위원회 위원)
  • 대한뇌전증학회 정회원 (역학위원회 위원)

논문

  •  Epidemiology and Healthcare Utilization in Pediatric Multiple Sclerosis and Neuromyelitis Optica: A Nationwide Population-Based Study in South Korea (2016-2020).  Children (Basel). 2024-05. 
  •  Incidence of Pediatric Acute Disseminated Encephalomyelitis During the Coronavirus Disease 2019 Pandemic in South Korea.  Pediatric Neurology. 2023-09. 
  •  Incidence of Guillain-Barré syndrome in South Korea during the early COVID-19 pandemic.  Frontiers in Neurology. 2023-02. 
  •  Mortality, disability, and prognostic factors of status epilepticus: a nationwide population-based retrospective cohort study.  Neurology. 2022-09. 
  •  Expanding the clinical phenotype and genetic spectrum of PURA-related neurodevelopmental disorders.  Brain & Development. 2021-10. 
  •  Impact of mobile health application on data collection and self-management of epilepsy.  Epilepsy & Behavior. 2021-06. 
  •  Deep Convolutional Neural Network Based Interictal-Preictal Electroencephalography Prediction: Application to Focal Cortical Dysplasia Type-II.  Frontiers in Neurology. 2020-11. 
  •  Characterization of Anti-seizure Medication Treatment Pathways in Pediatric Epilepsy Using the Electronic Health Record-Based Common Data Model.  Frontiers in Neurology. 2020-05. 
  •  Analysis of antiseizure drug-related reactions from the elctronic health record using the common data.  Epilepsia. 2020-04. 
  • Han JY, Choi SA, Chung YG, Shim YK, Kim WJ, Kim SY, Kim H, Lim BC, Hwang H, Chae JH, Choi J, Kim KJ. Change of centrotemporal spikes from onset to remission in self-limited epilepsy with centrotemporal spikes (SLECTS).  Brain Dev. 2020 Mar;42(3):270-276. 
  • Lee SA, Han SH, Cho YJ, Kim KT, Kim JE, Shin DJ, Seo JG, Kim YS, Ryu HU, Lee SY, Kim JB, Kang KW, Kim S, Kwon S, Kim J, Kim S, Kim HJ, Eun SH, Hur YJ, Choi SA, Yum MS, Park S, Kim JH, Lee GH, Kim YM, Hwang KJ, Kim EY, Yeon GM. Does the new Korean term for epilepsy reduce the stigma for Korean adults with epilepsy?.  Epilepsy Behav. 2020 Jan;102:106719. 
  • Choi SA, Cho A, Kim SY, Kim WJ, Shim YK, Lee JS, Jang SS, Lim BC, Kim H, Hwang H, Choi JE, Kim KJ, Kim MJ, Seong MW, Chae JH. Importance of early diagnosis in LMNA-related muscular dystrophy for cardiac surveillance.  Muscle Nerve. 2019 Dec;60(6):668-672. 
  • Choi SA, Kim KJ. The surgical and cognitive outcomes of focal cortical dysplasia.  J Korean Neurosurg Soc. 2019 May;62(3):321-327. 
  • Choi HS, Chung YG, Choi SA, Ahn S, Kim H, Yoon S, Hwang H, Kim KJ. Electroencephalographic resting-state functional connectivity of benign epilepsy with centrotemporal spikes.  J Clin Neurol. 2019 Apr;15(2):211-220. 
  • Choi SA, Kim SY, Kim WJ, Shim YK, Kim H, Hwang H, Choi JE, Lim BC, Chae JH, Chong S, Lee JY, Phi JH, Kim SK, Wang KC, Kim KJ. Antiepileptic Drug Withdrawal after Surgery in Children with Focal Cortical Dysplasia: Seizure Recurrence and Its Predictors.  J Clin Neurol. 2019 Jan;15(1):84-89. 
  • Choi SA, Kim SY, Kim H, Kim WJ, Kim H, Hwang H, Choi JE, Lim BC, Chae JH, Chong S, Lee JY, Phi JH, Kim SK, Wang KC, Kim KJ. Surgical outcome and predictive factors of epilepsy surgery in pediatric isolated focal cortical dysplasia.  Epilepsy Res. 2018 Jan;139:54-59. 
  • Choi SA, Kim SY, Yoon J, Choi J, Park SS, Seong MW, Kim H, Hwang H, Choi JE, Chae JH, Kim KJ, Kim S, Lee YJ, Nam SO, Lim BC. A unique mutational spectrum of MLC1 in Korean patients with megalencephalic leukoencephalopathy with subcortical cysts: p.Ala275Asp founder mutation and maternal uniparental disomy of chromosome 22.  Ann Lab Med. 2017 Nov;37(6):516-521.