모든 환자들이 건강하고 행복한 삶을 영위할 수 있도록 여러 의료진들과 긴밀히 협력하여 진료의 효율성을 극대화 하는데 최선을 다하고 있으며, 세계 유수의 기관들과의 정보교류와 연구를 통하여 의학을 선도하고 미래의 의료계를 이끌어갈 전문인력을 양성하는데 끊임없이 노력하고 있습니다.
2010 - 2013
일본 국립 신경정신 의료연구센터 (National Center for Neurology and Psychiatry) Department of Neuromuscular Research Research Fellow
2014 - 2018
이화여자대학교 의과대학 소아과학교실 조교수
2018 - 2020
이화여자대학교 의과대학 소아과학교실 부교수
수상
활동
대한소아과학회 정회원
대한소아신경학회 정회원
대한의학유전학회 정회원
대한신경근육질환학회 정회원
대한뇌전증학회 정회원
세계근육병학회 (World Muscle Society) 정회원
일반논문
1. 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.
2. Kim SY, Lim BC, Lee JS, Kim WJ, Kim H, Ko JM, Kim KJ, Choi SA, Kim H, Hwang H, Choi JE, Cho A, Moon J, Seong MW, Park SS, Lee YJ, Kim YO, Kim JS, Kim WS, Kwon YS, Park JD, Ahn Y, Hwang JY, Park HY, Lee Y, Choi M, Chae JH. The Korean undiagnosed diseases program: lessons from a one-year pilot project. Orphanet J Rare Dis. 2019 Mar 20;14(1):68.
3. Kim SY, Kim WJ, Kim H, Choi SA, Lee JS, Cho A, Jang SS, Lim BC, Kim KJ, Kim JI, Hahn SH, Chae JH. Collagen VI-related myopathy: Expanding the clinical and genetic spectrum. Muscle Nerve. 2018 Sep;58(3):381-388
4. Cho A, Malicdan MC, Miyakawa M, Nonaka I, Nishino I, Noguchi S. Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy. Hum Mol Genet. 2017 Aug 15;26(16):3081-3093.
5. Cho A, Seong MW, Lim BC, Lee HJ, Byeon JH, Kim SS, Kim SY, Choi SA, Wong AL, Lee J, Kim JS, Ryu HW, Lee JS, Kim H, Hwang H, Choi JE, Kim KJ, Hwang YS, Hong KH, Park S, Cho SI, Lee SJ, Park H, Seo SH, Park SS, Chae JH. Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center. Muscle Nerve. 2017 May;55(5):727-734.
6. Chae JH, Cho A. Floppy infant syndrome, in International Neurology (eds RP Lisak, DD Truong, WM Carroll and R Bhidayasiri), John Wiley & Sons, Ltd, Chichester, UK; 2016.
7. Chae JH, Vasta V, Cho A, Lim BC, Zhang Q, Eun SH, Hahn SH. Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders. J Med Genet. 2015 Mar;52(3):208-16.
8. Cho A, Hayashi YK, Monma K, Oya Y, Noguchi S, Nonaka I, Nishino I. Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy). J Neurol Neurosurg Psychiatry. 2014 Aug; 85(8):914-917.
9. Cho A, Noguchi S. Autophagy in GNE Myopathy. In: Bailly Y (ed.) Autophagy - A Double-Edged Sword - Cell Survival or Death? Rijeka: InTech; 2013.
10. Cho A, Kim SJ, Lim BC, Hwang H, Park JD, Kim GB, Jin DK, Lee J, Ki CS, Kim KJ, Hwang YS, Chae JH. Infantile Pompe disease: clinical and genetic characteristics with an experience of enzyme replacement therapy. J Child Neurol. 2012 Mar; 27(3):319-324
11. Lim BC, Ki CS, Kim JW, Cho A, Kim MJ, Hwang H, Kim KJ, Hwang YS, Park WY, Kim IO, Lee JS, Chae JH. Fukutin mutations in congenital muscular dystrophies with defective glycosylation of dystoglycan in Korea. Neuromuscul Disord, 2010 Aug; 20(8):524-30.
12. Kim H, Cho A, Lim BC, Kim MJ, Kim KJ, Nishino I, Hwang YS, Chae JH. A 13-year-old girl with proximal weakness and hypertrophic cardiomyopathy with Danon disease. Muscle Nerve. 2010 Jun; 41(6):879-82.