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1. The First Korean case of combined oxidative phosphorylation deficiency-17 diagnosed by clinical and molecular investigation   
Young A Kim, Yoo-Mi Kim, Yun-Jin Lee, Chong Kun Cheon
Korean J Pediatr. 2017 December;60(12):408-412.  Publication Date (Online): 2017 December 15
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2. Neurofibromatosis type I: a single centers experience in Korea   
Min Jeong Kim, Chong Kun Cheon
Korean J Pediatr. 2014 September;57(9):410-415.  Publication Date (Online): 2014 June 04
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3. Prader-Willi syndrome: a single centers experience in Korea   
Yea Ji Kim, Chong Kun Cheon
Korean J Pediatr. 2014 July;57(7):310-316.  Publication Date (Online): 2014 March 14
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4. Two adolescent patients with coexistent Graves' disease and Moyamoya disease in Korea   
Chong Kun Cheon, Su Yung Kim, Jae-Ho Yoo
Korean J Pediatr. 2014 June;57(6):287-291.  Publication Date (Online): 2014 June 15
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5. The natural history and prognostic factors of Graves' disease in Korean children and adolescents   
Seung Min Song (Song SM), Ji-Seok Youn (Youn JS), Jung Min Ko (Ko JM), Chong Kun Cheon (Cheon CK), Jin-Ho Choi (Choi JH), Han Wook Yoo (Yoo HW)
Korean J Pediatr. 2010 April;53(4):585-591.
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6. Epidemic acute interstitial pneumonia in children occurred during the early 2006s   
Chong Kun Cheon (Cheon CK), Hyun-Seung Jin (Jin HS), Eun Kyeong Kang (Kang EK), Hyo Bin Kim (Kim HB), Byoung-Joo Kim (Kim BJ), Jinho Yu (Yu JH), Seong Jong Park (Park SJ), Soo-Jong Hong (Hong SJ), June Dong Park (Park JD)
Korean J Pediatr. 2008 April;51(4):383-390.
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