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Showing results 1 to 5 of 5

Issue Date	Title / Author(s) / Citation	File
2002	Mutation analysis of MECP2 and clinical characterization in Korean patients with Rett syndrome Chae, Jong Hee; Hwang, Yong Seung; Kim, Ki Joong J Child Neurol 2002;17:33-36	link
2007-11	Identification of a novel DHCR7 mutation in a Korean patient with Smith-Lemli-Opitz syndrome Chae, Jong Hee; Kim, Ki Joong; Hwang, Yong Seung; Ki, Chang-Seok; Kim, Jong-Won J Child Neurol. 2007 Nov;22(11):1297-300.	link
2010-06	Cerebellum Can Be a Possible Generator of Progressive Myoclonus Koh, Kyung Nam; Lim, Byung Chan; Hwang, Hee; Park, June Dong; Kim, Ki Joong; Kim, Seung-Ki; Moon, Han Ku; Wang, Kyu-Chang; Hwang, Yong-Seung; Chae, Jong Hee JOURNAL OF CHILD NEUROLOGY; Vol.25 6; 728-731	DOI
2010-08	Ischemic Stroke in a 7-Month-Old Infant With Antiphospholipid Antibody and Homozygous C677T Methylenetetrahydrofolate Reductase (MTHFR) Polymorphism Kim, Se Hee; Hwang, Hee; Chae, Jong Hee; Kim, Ki Joong; Lim, Byung Chan; Hwang, Yong Seung JOURNAL OF CHILD NEUROLOGY; Vol.25 8; 1047-1050	DOI
2020-03	Serum α-synuclein and IL-1β are increased and correlated with measures of disease severity in children with epilepsy: potential prognostic biomarkers? Choi, Jieun; Kim, Soo Yeon; Kim, Hunmin; Lim, Byung Chan; Hwang, Hee; Chae, Jong Hee; Kim, Ki Joong; Oh, Sohee; Kim, Eun Young; Shin, Jeon-Soo BMC Neurology, 20(1):85	view file DOI