Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Kee Hyuck, Kim"'
Autor:
Hyesun Hyun, Yo Han Ahn, Eujin Park, Hyun Jin Choi, Kyoung Hee Han, Jung Won Lee, Su Young Kim, Eun Mi Yang, Jin Soon Suh, Jae Il Shin, Min Hyun Cho, Ja Wook Koo, Kee Hyuck Kim, Hye Won Park, Il Soo Ha, Hae Il Cheong, Hee Gyung Kang, Seong Heon Kim
Publikováno v:
Childhood Kidney Diseases, Vol 27, Iss 2, Pp 97-104 (2023)
Purpose Angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers (ARBs) are frequently employed to counteract the detrimental effects of proteinuria on glomerular diseases. However, the effects of ARBs remain poorly examined in p
Externí odkaz:
https://doaj.org/article/64a6880ba82b4db0ab0f73cb34700b0e
Autor:
Sukdong Yoo, Min Hyun Cho, Hee Sun Baek, Ji Yeon Song, Hye Sun Lee, Eun Mi Yang, Kee Hwan Yoo, Su Jin Kim, Jae Il Shin, Keum Hwa Lee, Tae-Sun Ha, Kyung Mi Jang, Jung Won Lee, Kee Hyuck Kim, Heeyeon Cho, Mee Jeong Lee, Jin-Soon Suh, Kyoung Hee Han, Hye Sun Hyun, Il-Soo Ha, Hae Il Cheong, Hee Gyung Kang, Mee Kyung Namgoong, Hye-Kyung Cho, Jae-Hyuk Oh, Sang Taek Lee, Kyo Sun Kim, Joo Hoon Lee, Young Seo Park, Seong Heon Kim
Publikováno v:
Kidney Research and Clinical Practice, Vol 40, Iss 4, Pp 673-686 (2021)
Background The clinical features of pediatric rhabdomyolysis differ from those of the adults with rhabdomyolysis; however, multicenter studies are lacking. This study aimed to investigate the characteristics of pediatric rhabdomyolysis and reveal the
Externí odkaz:
https://doaj.org/article/f82f28b155a940f2ba694a67e910019c
Autor:
Peong Gang Park, Kee Hyuck Kim, Hye Sun Hyun, Chan Hee Lee, Jin-Su Park, Jeong Hae Kie, Young Hun Choi, Kyung Chul Moon, Hae Il Cheong
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-7 (2018)
Abstract Background Multicentric carpotarsal osteolysis syndrome (MCTO) is characterized by progressive destruction and disappearance of the carpal and tarsal bones associated with nephropathy. MCTO is caused by loss-of-function mutations in the MAF
Externí odkaz:
https://doaj.org/article/81760b63d94c4f478bd99538da6db214
Autor:
Kee Hyuck Kim
Publikováno v:
Childhood Kidney Diseases, Vol 20, Iss 1, Pp 6-10 (2016)
Poststreptococcal glomerulonephritis (PSGN) is one of the most recognized diseases in pediatric nephrology. Typical clinical features include rapid onset of gross hematuria, edema, and hypertension, and cases are typically preceded by an episode of g
Externí odkaz:
https://doaj.org/article/c1a35f8634d643d6b655ffbc85cbaab3
Publikováno v:
Childhood Kidney Diseases, Vol 19, Iss 2, Pp 159-166 (2015)
Purpose: The aim of the present study was to investigate the risk factors for the development of coronary artery lesions (CALs) and to determine whether hyponatremia is associated with CALs in children with Kawasaki disease (KD). Methods: We retrospe
Externí odkaz:
https://doaj.org/article/2e68797287a243288ca65531b43cbb65
Autor:
Jiwon M. Lee, Younghwa Jung, Se Eun Lee, Jun Ho Lee, Kee Hyuck Kim, Ja Wook Koo, Young Seo Park, Hae Il Cheong, Il-Soo Ha, Yong Choi, Hee Gyung Kang
Publikováno v:
Korean Journal of Pediatrics, Vol 56, Iss 7, Pp 282-285 (2013)
PurposeRecent studies have established the association between hypotonic fluids administration and hospital-acquired hyponatremia in children. The present paper investigated the pattern of current practice in intravenous fluid prescription among Kore
Externí odkaz:
https://doaj.org/article/34ea2de6a17e44949bd572da06c00752
Autor:
Mee Jeong Lee, Hae Il Cheong, Jin-Soon Suh, Hee Yeon Cho, Myung Hyun Cho, Hye Sun Hyun, Ji Won Lee, Seong Heon Kim, Yo Han Ahn, Eun Mi Yang, Il-Soo Ha, Hee Gyung Kang, Min Hyun Cho, Woo Yeong Chung, Jung Won Lee, Kee Hwan Yoo, Ji Hyun Kim, Kee Hyuck Kim
Publikováno v:
Pediatric Nephrology. 36:701-709
Children with nephrotic syndrome (NS) are at an increased risk of acute kidney injury (AKI) and the incidence of AKI in this population is reportedly increasing. This study aimed to investigate the incidence, clinical profiles, and risk factors of AK
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bbc1a733d55c49dded51aabb4f02955
https://doi.org/10.1007/s00467-020-04740-y
https://doi.org/10.1007/s00467-020-04740-y
Publikováno v:
Korean Journal of Pediatrics, Vol 55, Iss 5, Pp 181-184 (2012)
Voiding cystourethrography (VCUG) is a commonly performed diagnostic procedure for the evaluation of vesicoureteral reflux with urinary tract infection or congenital renal diseases in children. The procedure is relatively simple and cost-effective, a
Externí odkaz:
https://doaj.org/article/c93e6c24a6a64b3999849e03870c6f2c
Autor:
Eun Mi, Yang, Kee Hwan, Yoo, Yo Han, Ahn, Seong Heon, Kim, Jung Won, Lee, Woo Yeong, Chung, Min Hyun, Cho, Kee Hyuck, Kim, Heeyeon, Cho, Mee Jeong, Lee, Jin-Soon, Suh, Hye Sun, Hyun, Jiwon M, Lee, Myung Hyun, Cho, Ji Hyun, Kim, Il-Soo, Ha, Hae Il, Cheong, Hee Gyung, Kang
Publikováno v:
Pediatric nephrology (Berlin, Germany). 36(3)
Children with nephrotic syndrome (NS) are at an increased risk of acute kidney injury (AKI) and the incidence of AKI in this population is reportedly increasing. This study aimed to investigate the incidence, clinical profiles, and risk factors of AK
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0ec383a923220aec3721e074001d7fde
https://pubmed.ncbi.nlm.nih.gov/32888043
https://pubmed.ncbi.nlm.nih.gov/32888043
Autor:
Kee Hyuck Kim, Kyung Chul Moon, Jin Su Park, Chan Hee Lee, Young Hun Choi, Hye Sun Hyun, Peong Gang Park, Hae Il Cheong, Jeong Hae Kie
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-7 (2018)
BMC Medical Genetics
BMC Medical Genetics
Background Multicentric carpotarsal osteolysis syndrome (MCTO) is characterized by progressive destruction and disappearance of the carpal and tarsal bones associated with nephropathy. MCTO is caused by loss-of-function mutations in the MAF bZIP tran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c187f6a3769cc44df0738fa5e80ebbb
http://link.springer.com/article/10.1186/s12881-018-0682-x
http://link.springer.com/article/10.1186/s12881-018-0682-x