Výsledky vyhledávání - "Eun-Jung Cheon"

Akademický článek

Anterior uveitis as an early diagnostic marker in incomplete Kawasaki disease

Autor: Kyung Ok Ko, Eun Jung Cheon

Publikováno v: BMC Pediatrics, Vol 24, Iss 1, Pp 1-8 (2024)

Abstract Background Kawasaki disease (KD) is a significant cause of acquired heart disease in children, particularly in developed countries. Incomplete Kawasaki disease (IKD) lacks some of the classic KD symptoms, complicating diagnosis. This study e

Externí odkaz: https://doaj.org/article/09f44e02bbc44ab9843a710e3a14cec9

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Akademický článek

P wave dispersion on 12-lead electrocardiography in adolescents with neurocardiogenic syncope

Autor: Dong-Hyuk Lee, Kyung-Min Lee, Jung-Min Yoon, Jae-Woo Lim, Kyung-Ok Kho, Hong-Ryang Kil, Eun-Jung Cheon

Publikováno v: Korean Journal of Pediatrics, Vol 59, Iss 11, Pp 451-455 (2016)

PurposeNeurocardiogenic syncope (NCS) is the most frequent cause of fainting during adolescence. Inappropriate cardiovascular autonomic control may be responsible for this clinical event. The head-up tilt test has been considered a diagnostic standar

Externí odkaz: https://doaj.org/article/2c501ea3dd37457ab75ffe9875d1444d

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Akademický článek

Hemolytic anemia associated with intravenous immunoglobulin in Kawasaki disease

Autor: Eun Jung Cheon, Jun Suk Oh

Publikováno v: BMC Pediatrics, Vol 24, Iss 1, Pp 1-6 (2024)

Abstract Background The administration of high-dose intravenous immunoglobulin (IVIG) is a standard treatment for the management of Kawasaki disease (KD). IVIG is known to be a highly effective and safe treatment. Case presentation We report the deve

Externí odkaz: https://doaj.org/article/7ab3ba95e8d940f5b7f7a888e9e90c58

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Akademický článek

Reliability of renal point-of-care ultrasound (POCUS) performed by pediatric postgraduates to diagnose hydronephrosis in infants

Autor: Eun Jung Cheon, Jung Min Yoon

Publikováno v: Frontiers in Pediatrics, Vol 12 (2024)

PurposePoint-of-care ultrasound (POCUS) has gained prominence in a variety of medical specialties due to advances in ultrasound technology. POCUS has not been fully integrated into pediatric residency training programs despite its widespread use and

Externí odkaz: https://doaj.org/article/261f84edffe34cdbba93d975d893c284

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Akademický článek

A case report of tubulointerstitial nephritis and uveitis syndrome in children with an unfavorable outcome

Autor: Sang I Kong, Mun Hyang Park, Eun Jung Cheon

Publikováno v: Childhood Kidney Diseases, Vol 27, Iss 1, Pp 40-45 (2023)

Tubulointerstitial nephritis and uveitis (TINU) syndrome is defined as the occurrence of tubulointerstitial nephritis and uveitis in the absence of other systemic diseases. Three pediatric cases have been reported in the Republic of Korea, and we now

Externí odkaz: https://doaj.org/article/dc784917013b45dda33d63b46d611c51

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Akademický článek

A decision tree model for predicting intravenous immunoglobulin resistance and coronary artery involvement in Kawasaki disease

Autor: Jinwoon Joung, Jun Suk Oh, Jung Min Yoon, Kyung Ok Ko, Gyeong Hee Yoo, Eun Jung Cheon

Publikováno v: BMC Pediatrics, Vol 22, Iss 1, Pp 1-7 (2022)

Abstract Objectives This study aims to develop a new algorithm for predicting intravenous immunoglobulin (IVIG) resistance and coronary artery involvement in Kawasaki disease (KD) through decision tree models. Methods Medical records of children hosp

Externí odkaz: https://doaj.org/article/3d097a4478a94ea284dcad8e1b9ea97f

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Akademický článek

Delta neutrophil index as a predictor of vesicoureteral reflux in children with febrile urinary tract infection

Autor: Jae Eun Kim, Jun Suk Oh, Jung Min Yoon, Kyung Ok Ko, Eun Jung Cheon

Publikováno v: Childhood Kidney Diseases, Vol 26, Iss 1, Pp 46-51 (2022)

Purpose Delta neutrophil index (DNI) indicates immature granulocytes in peripheral blood and has been confirmed to be effective as a prognostic factor for neonatal sepsis. Also, it has been reported to have diagnostic value in acute pyelonephritis an

Externí odkaz: https://doaj.org/article/408a17b8be584116ba3f9a98f10852c0

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Akademický článek

A Case of Idiopathic Renal Hypouricemia with Gene Mutation Showing General Weakness and Incidental Renal Stone

Autor: Jin Woon Joung, Young Wha Song, Jong Dae Kim, Eun Jung Cheon

Publikováno v: Childhood Kidney Diseases, Vol 25, Iss 1, Pp 44-48 (2021)

Idiopathic renal hypouricemia (iRHUC) is a rare hereditary disease caused by a defect in urate handling of renal tubules. Type 1 renal hypouricemia (RHUC1) is diagnosed with confirmation of a mutation in SLC22A12 gene which encodes a renal urate-anio

Externí odkaz: https://doaj.org/article/e3279cd080d24c7bb5e849058bec4046

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Akademický článek

14q12q13.3 Deletion Diagnosed Using Chromosomal Microarray Analysis in an Infant Showing Seizures, Hypoplasia of the Corpus Callosum, and Developmental Delay

Autor: Jae Hyuk Kwon, Young Hwa Song, Jung Min Yoon, Eun Jung Cheon, Kyung Ok Ko, Jae Woo Lim, Hyon J. Kim

Publikováno v: Neonatal Medicine, Vol 27, Iss 4, Pp 207-213 (2020)

14q12q13.3 Deletion is a rare microdeletion syndrome associated with neurodevelopmental delay, failure to thrive, seizures, and abnormal brain development. Symptoms vary depending on the sites of gene deletion, and establishing the diagnosis is often

Externí odkaz: https://doaj.org/article/81f6d91133e840e59be76b45335bf34f

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