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Table of Contents | December, 2010  Vol. 53 No.12 Previous Issue | Next Issue | Archive
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Review Article
Lung interstitial cells during alveolarization   
Chang Won Choi (Choi CW)
Korean J Pediatr. 2010 December;53(12):979-984.
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Neonatal innate immunity and Toll-like receptor   
Hye Sun Yoon (Yoon HS)
Korean J Pediatr. 2010 December;53(12):985-988.
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Ureaplasma infections in pre-term infants: Recent information regarding the role of Ureaplasma species as neonatal pathogens   
Tae-Jung Sung (Sung TJ)
Korean J Pediatr. 2010 December;53(12):989-993.
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Original Article
Risk factors of ocular involvement in children with mitochondrial respiratory chain complex defect   
Jung Hyun Chae (Chae JH), Jung Hun Lee (Lee JH), Kyo Ryung Kim (Kim KR), Suk Ho Byeon (Byeon SH), Young Mock Lee (Lee YM), Hoon Heung Dong (Dong HH), Joon Soo Lee (Lee JS), Heung Dong Kim (Kim HD)
Korean J Pediatr. 2010 December;53(12):994-999.
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Therapeutic monitoring of vancomycin according to initial dosing regimen in pediatric patients   
Dae Il Kim (Kim DI), Mi Sun Im (Im MS), Jin Hyoung Choi (Choi JH), Jina Lee (Lee Jn), Eun Hwa Choi (Choi EH), Hoan Jong Lee (Lee HJ)
Korean J Pediatr. 2010 December;53(12):1000-1005.
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What is the 'objective' differential factor of diarrhea in infancy?: Normal state versus diarrheal illness in infants with chronic frequent and loose stool   
Jin-Bok Hwang (Hwang JB), Kyung Ji Kang (Kang KJ), Jung Jeung Lee (Lee JJ), Ae Suk Kim (Kim AS)
Korean J Pediatr. 2010 December;53(12):1006-1011.
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Clinical outcome of transcatheter closure of patent ductus arteriosus in small children weighing 10 kg or less   
Young A Park (Park YA), Nam Kyun Kim (Kim NK), Su-Jin Park (Park SJ), Bong Sic Yun (Yun BS), Jae Young Choi (Choi JY), Jun Hee Sul (Sul JH)
Korean J Pediatr. 2010 December;53(12):1012-1017.
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Case Report
A family with Townes-Brocks syndrome with congenital hypothyroidism and a novel mutation of the SALL1 gene   
Won Ik Choi (Choi WI), Ji Hye Kim (Kim JH), Han Wook Yoo (Yoo HW), Sung Hee Oh (Oh SH)
Korean J Pediatr. 2010 December;53(12):1018-1021.
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A case of thanatophoric dysplasia type I with an R248C mutation in the FGFR3 gene   
Eun Jung Noe (Noe EJ), Han Wook Yoo (Yoo HW), Kwang Nam Kim (Kim KN), So Yeon Lee (Lee SY)
Korean J Pediatr. 2010 December;53(12):1022-1025.
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