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Novel Mutation of SLC26A3 Gene Observed in Congenital Chloride Diarrhea

Cheon JH, Yu NL, Lee NM

Congenital chloride diarrhea (CLD) is a rare autosomal recessive disease caused by mutations in the solute carrier family 26 member 3 (SLC26A3) gene on chromosome 7q31. Affected neonates are vulnerable...
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The Success of Brain Magnetic Resonance Imaging in Non-Sedated Infants

Yu NL, Lee HM, Kim HG, Kim SY

Objective: This study aimed to evaluate the success rate of brain magnetic resonance imaging (MRI) in non-sedated at a single neonatal intensive care unit (NICU). Methods: Infants underwent brain MRI following...
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Predictive Factors for Severe Thrombocytopenia and Classification of Causes of Thrombocytopenia in Premature Infants

Shin HB, Yu NL, Lee NM, Yi DY, Yun SW, Chae SA, Lim IS

PURPOSE: This study investigated predictive factors for severe neonatal thrombocytopenia, which greatly increases the need for intensive care and is associated with a high mortality rate in premature infants. Factors...
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