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REVIEW ARTICLE 2017 March 15
Genetics of hereditary nephrotic syndrome: a clinical review
Advances in podocytology and genetic techniques have expanded our understanding of the pathogenesis of hereditary steroid-resistant nephrotic syndrome (SRNS). In the past 20 years, over 45 genetic mutations have been identified in patients with hereditary SRNS. Genetic mutations...
ORIGINAL ARTICLE 2017 March 15
Postdischarge growth assessment in very low birth weight infants
Purpose: The goal of nutritional support for very-low-birth-weight (VLBW) infants from birth to term is to match the in utero growth rates; however, this is rarely achieved. Methods: We evaluated postdischarge growth patterns and growth failure in 81 Korean VLBW infants ...
ORIGINAL ARTICLE 2017 March 15
Maternal food restrictions during breastfeeding
Purpose: This study investigated self-food restriction during breastfeeding, reviewed the literature showing the effect of maternal diet on the health of breast-fed infants, and explored the validity of dietary restrictions. Methods: Questionnaire data were collected from breas...
ORIGINAL ARTICLE 2017 March 15
Etiology and clinical characteristics of fever of unknown origin in children: a 15-year experience in a single center
Purpose: Fever is one of the most common symptoms in children. In previous studies, infectious disease was the most common cause of pediatric fever of unknown origin (FUO). The aim of this study is to investigate the etiology, clinical characteristics and prognosis of pediatric ...
ORIGINAL ARTICLE 2017 March 15
Posttransplantation lymphoproliferative disorder after pediatric solid organ transplantation: experiences of 20 years in a single center
Purpose: To evaluate the clinical spectrum of posttransplantation lymphoproliferative disorder (PTLD) after solid organ transplantation (SOT) in children. Methods: We retrospectively reviewed the medical records of 18 patients with PTLD who underwent liver (LT) or kidney transp...
CASE REPORT 2017 March 15
A compound heterozygous mutation in the FMO3 gene: the first pediatric case causes fish odor syndrome in Korea
Trimethylaminuria (TMAuria), known as fish odor syndrome, is a congenital metabolic disorder characterized by an odor resembling that of rotting fish. This odor is caused by the secretion of trimethylamine (TMA) in the breath, sweat, and body secretions and the excretion of T...
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eISSN : 2092-7258
pISSN : 1738-1061
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Volume 60 (3); Mar 2017
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Noonan syndrome and Rasopathies: clinical features, diagnosis and management   
Beom Hee Lee, Yoo Han Wook
Received 2012 Aug 20     Accepted 2012 Dec 24.    KJP-12-068 - Withdrawal
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