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Asymptomatic maternal 3-methylcrotonylglycinuria detected by her unaffected baby's neonatal screening test
Sun Hee Lee, Yong Hee Hong
Korean J Pediatr. 2014;57(7):329-332.   Published online July 23, 2014
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A chromosome 1q44 deletion in a 4-month-old girl; The first report in Korea
Joo Hyun Cho, Eun Song Song, Hee Na Kim, Burm Seok Oh, Young Youn Choi
Korean J Pediatr. 2014;57(6):292-296.   Published online June 30, 2014
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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;57(6):287-291.   Published online June 30, 2014
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Gastrointestinal hemangioma in childhood: a rare cause of gastrointestinal bleeding
Eon Chul Han, Soo-Hong Kim, Hyun-Young Kim, Sung-Eun Jung, Kwi-Won Park
Korean J Pediatr. 2014;57(5):245-249.   Published online May 31, 2014
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Identification of a novel mutation in a patient with pseudohypoparathyroidism type Ia
Ye Seung Lee, Hui Kwon Kim, Hye Rim Kim, Jong Yoon Lee, Joong Wan Choi, Eun Ju Bae, Phil Soo Oh, Won Il Park, Chang Seok Ki, Hong Jin Lee
Korean J Pediatr. 2014;57(5):240-244.   Published online May 31, 2014
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Pulmonary hemorrhage in pediatric lupus anticoagulant hypoprothrombinemia syndrome
Ji Soo Kim, Min Jae Kim, E Young Bae, Dae Chul Jeong
Korean J Pediatr. 2014;57(4):202-205.   Published online April 30, 2014
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Percutaneous ultrasound-guided thrombin injection is effective even in infants with external iliac artery pseudoaneurysms
Min-Jung Cho, Ung-Bae Jeon, Ki-Seok Choo, Hyoung-Doo Lee
Korean J Pediatr. 2014;57(4):199-201.   Published online April 30, 2014
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Toxic epidermal necrolysis induced by lamotrigine treatment in a child
Youngsuk Yi, Jeong Ho Lee, Eun Sook Suh
Korean J Pediatr. 2014;57(3):153-156.   Published online March 31, 2014
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Congenital muscular dystrophy type 1A with residual merosin expression
Hyo Jeong Kim, Young-Chul Choi, Hyung Jun Park, Young-Mock Lee, Heung Dong Kim, Joon Soo Lee, Hoon-Chul Kang
Korean J Pediatr. 2014;57(3):149-152.   Published online March 31, 2014
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Shiga toxin-associated hemolytic uremic syndrome complicated by intestinal perforation in a child with typical hemolytic uremic syndrome
Hye Jin Chang, Hwa Young Kim, Jae Hong Choi, Hyun Jin Choi, Jae Sung Ko, Il Soo Ha, Hae Il Cheong, Yong Choi, Hee Gyung Kang
Korean J Pediatr. 2014;57(2):96-99.   Published online February 24, 2014
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Griscelli syndrome type 2: a novel mutation in RAB27A gene with different clinical features in 2 siblings: a diagnostic conundrum
Kirtisudha Mishra, Shilpy Singla, Suvasini Sharma, Renu Saxena, Vineeta Vijay Batra
Korean J Pediatr. 2014;57(2):91-95.   Published online February 24, 2014
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A novel PRF1 gene mutation in a fatal neonate case with type 2 familial hemophagocytic lymphohistiocytosis
Jae Yeon Kim, Jeong Hee Shin, Se In Sung, Jin Kyu Kim, Ji Mi Jung, So Yoon Ahn, Eun Sun Kim, Ja-Young Seo, Eun-Sook Kang, Sun-Hee Kim, Hee-Jin Kim, Yun Sil Chang, Won Soon Park
Korean J Pediatr. 2014;57(1):50-53.   Published online January 31, 2014
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Identification of a novel mutation in the CHD7 gene in a patient with CHARGE syndrome
Yeonkyung Kim, Ho-Seok Lee, Jung-Seok Yu, Kangmo Ahn, Chang-Seok Ki, Jihyun Kim
Korean J Pediatr. 2014;57(1):46-49.   Published online January 31, 2014
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Moyamoya syndrome occurred in a girl with an inactive systemic lupus erythematosus
Yun-Jin Lee, Gyu Min Yeon, Sang Ook Nam, Su Yung Kim
Korean J Pediatr. 2013;56(12):545-549.   Published online December 20, 2013
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Asymptomatic moyamoya syndrome, atlantoaxial subluxation and basal ganglia calcification in a child with Down syndrome
Kyung Yeon Lee, Kun-Soo Lee, Young Cheol Weon
Korean J Pediatr. 2013;56(12):540-543.   Published online December 20, 2013
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