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Original Article
Critical Care Medicine
Assessment of interhospital transport care for pediatric patients
Krittiya Chaichotjinda, Marut Chantra, Uthen Pandee
Clin Exp Pediatr. 2020;63(5):184-188.   Published online August 29, 2019
Background: Many critically ill patients require transfer to a higher-level hospital for complex medical care. Despite the publication of the American Academy of Pediatrics guidelines for pediatric interhospital transportation services and the establishment of many pediatric transport programs, adverse events during pediatric transport still occur.
Purpose: To determine the incidence of adverse events occurring during pediatric transport and explore their complications...
Case Report
Transient carnitine transport defect with cholestatic jaundice: report of one case in a premature baby
Hyun-Seok Cho, Young Kwang Choo, Hong Jin Lee, Hyeon-Soo Lee
Clin Exp Pediatr. 2012;55(2):58-62.   Published online February 14, 2012

Carnitine (β-hydroxy-γ-trimethylaminobutyric acid) is involved in the transport of long-chain fatty acids into the mitochondrial matrix and the removal of potentially toxic acylcarnitine esters. Transient carnitine transport defect is a rare condition in newborns reported in 1/90,000 live births. In this paper, we describe a case of transient carnitine transport defect found in a premature baby who had prolonged cholestatic...

Review Article
Regionalization of neonatal intensive care in Korea
Yun Sil Chang
Clin Exp Pediatr. 2011;54(12):481-488.   Published online December 31, 2011

In the current era of low-birth rate in Korea, it is important to improve our neonatal intensive care and to establish an integrative system including a regional care network adequate for both high-risk pregnancies and high-risk newborn infants. Therefore, official discussion for nation-wide augmentation, proper leveling, networking, and regionalization of neonatal and perinatal care is urgently needed. In this report,...

Case Report
A case of idiopathic renal hypouricemia
Moon Hee Han, Sang Uk Park, Deok-Soo Kim, Jae Won Shim, Jung Yeon Shim, Hye Lym Jung, Moon Soo Park
Clin Exp Pediatr. 2007;50(5):489-492.   Published online May 15, 2007
Idiopathic renal hypouricemia is a disorder characterized by impaired urate handling in the renal tubules. This disease usually produces no symptoms, but hematuria, uric acid nephrolithiasis or acute renal failure may develop. A defect in the SLC22A12 gene, which encodes the human urate transporter, is the known major cause of this disorder. We describe a 10-month-old boy with idiopathic renal...
Original Article
Sodium and calcium transport in spherocytic red blood cells.
Shin Heh Kang, Kir Young Kim, Young Ho Lee, Bok Soon Kang
Clin Exp Pediatr. 1991;34(7):978-991.   Published online July 31, 1991
Hereditary spherocytosis (HS) is an autosomal, dominantly inherited hemolytic disorder which shows characteristic spherocytes on peripheral smear. As spherocytes are rounder, more fragile and susceptible to extravascular hemolysis in the spleen, HS patients suffer from variable degrees of anemia, jaundice, splenomegaly and gall stones. However the pathogenesis is heterogenous in HS, such as spectrin deficiency, decreased spectrin-protein 4.1 binding, increased spectrin binding to the RBC...