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Association between respiratory viruses and asthma exacerbations

Kim WK

No abstract available.
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Identification of a novel mutation in the CHD7 gene in a patient with CHARGE syndrome

Kim Y, Lee HS, Yu JS, Ahn K, Ki CS, Kim J

CHARGE syndrome has been estimated to occur in 1:10,000 births worldwide and shows various clinical manifestations. It is a genetic disorder characterized by a specific and a recognizable pattern of...
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Channelopathies

Kim JB

Channelopathies are a heterogeneous group of disorders resulting from the dysfunction of ion channels located in the membranes of all cells and many cellular organelles. These include diseases of the...
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The correlation of blood pressure with height and weight in Korean adolescents aged 10-19 years; The Korean National Health and Nutrition Examination Surveys (2009-2011)

Song YH

PURPOSE: Height-specific blood pressure (BP) is the standard parameter used to diagnose childhood hypertension. However, there has been some argument that weight may be a better variable than height in...
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Kidney size estimation in Korean children with Technesium-99m dimercaptosuccinic acid scintigraphy

Lee MJ, Son MK, Kwak BO, Park HW, Chung S, Kim KS

PURPOSE: Renal size is an important indicator to determine adequate organ growth in children. The aim of this study was to estimate renal size with Technesium-99m dimercaptosuccinic acid (DMSA) scan...
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Prevalence of respiratory viral infection in children hospitalized for acute lower respiratory tract diseases, and association of rhinovirus and influenza virus with asthma exacerbations

Kwon JM, Shim JW, Kim DS, Jung HL, Park MS, Shim JY

PURPOSE: In this study, we aimed to investigate the prevalence of year-round respiratory viral infection in children with lower respiratory tract infection (LRTI) and the relationship between respiratory viral infection...
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A novel PRF1 gene mutation in a fatal neonate case with type 2 familial hemophagocytic lymphohistiocytosis

Kim JY, Shin JH, Sung SI, Kim JK, Jung JM, Ahn SY, Kim ES, Seo JY, Kang ES, Kim SH, Kim HJ, Chang YS, Park WS

Hemophagocytic lymphohistiocytosis (HLH) occurs in the primary form (genetic or familial) or secondary form (acquired). The familial form of HLH (FHL) is a potentially fatal autosomal recessive disorder that occurs...
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Primary repair of symptomatic neonates with tetralogy of Fallot with or without pulmonary atresia

Lee CH, Kwak JG, Lee C

Recently, surgical outcomes of repair of tetralogy of Fallot (TOF) have improved. For patients with TOF older than 3 months, primary repair has been advocated regardless of symptoms. However, a...
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