Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Eun Jung Cheon"'
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
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
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
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
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
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
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
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss 7, Pp 298-302 (2016)
PurposeRecent reports showed that plasma N-terminal pro-brain natriuretic peptide (NT-proBNP) could be a useful biomarker of intravenous immunoglobulin (IVIG) unresponsiveness and coronary artery lesion (CAL) development in Kawasaki disease (KD). The
Externí odkaz:
https://doaj.org/article/0a93ba07c48d448ea121957385527839
Publikováno v:
Korean Journal of Pediatrics, Vol 57, Iss 12, Pp 542-545 (2014)
Bickerstaff's brainstem encephalitis is characterized by ophthalmoplegia, ataxia, and disturbance of consciousness. It is similar to Miller Fisher syndrome, a variant of Guillain-Barre syndrome, in that they share features such as ophthalmoplegia and
Externí odkaz:
https://doaj.org/article/b7fc64a55a174eee9bded4f482d6355a
Autor:
Jin Hwan Lee, Jung Min Yoon, Jae Woo Lim, Kyung Og Ko, Seong Jun Choi, Jong-Yeup Kim, Eun Jung Cheon
Publikováno v:
Korean Journal of Pediatrics, Vol 57, Iss 11, Pp 484-488 (2014)
PurposeChronic upper airway obstruction causes hypoxemic pulmonary vasoconstriction, which may lead to right ventricle (RV) dysfunction. Adenotonsillar hypertrophy (ATH) is the most common cause of upper airway obstruction in children. Therefore, we
Externí odkaz:
https://doaj.org/article/7c8725ea7a0e405bb8fb0d1c6afe1814