Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jiwon M. Lee"'
Publikováno v:
Childhood Kidney Diseases, Vol 25, Iss 2, Pp 92-111 (2021)
Purpose Nephrotic syndrome (NS) is the most common form of glomerulopathy in children. Most pediatric patients respond to glucocorticosteroid treatment (steroid-sensitive NS, SSNS), while approximately 10–15% will remain unresponsive or later becom
Externí odkaz:
https://doaj.org/article/f7bc745b82104365ba99eea59c33780f
Autor:
Yunsoo Choe, Jiwon M. Lee, Ji Hyun Kim, Myung Hyun Cho, Seong Heon Kim, Joo Hoon Lee, Young Seo Park, Hee Gyung Kang, Il Soo Ha, Hae Il Cheong
Publikováno v:
Childhood Kidney Diseases, Vol 23, Iss 2, Pp 59-66 (2019)
Background Primary hyperoxaluria (PH), a rare inborn error of glyoxylate meta bolism causing overproduction of oxalate, is classified into three genetic subgroups: type 1–3 (PH1–PH3) caused by AGXT, GRHPR, and HOGA1 gene mutations, respectively.
Externí odkaz:
https://doaj.org/article/6a37a2313c8747a8873ada218cfc5a33
Autor:
Jiwon M. Lee
Publikováno v:
Childhood Kidney Diseases, Vol 22, Iss 1, Pp 12-16 (2018)
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital malformation syndrome that is characterized by a triad of uterine didelphys, blind hemivagina, and ipsilateral renal agenesis. There is a wide variety of phenotypic presentation which is re
Externí odkaz:
https://doaj.org/article/9706cc9604ed48b2a9e5a25bb7fc7d56
Autor:
Jiwon M. Lee, Jae Won Yang, Andreas Kronbichler, Michael Eisenhut, Gaeun Kim, Keum Hwa Lee, Jae Il Shin
Publikováno v:
Journal of Immunology Research, Vol 2019 (2019)
Introduction. The soluble urokinase-type plasminogen activator receptor (suPAR) has been found to be elevated in primary focal segmental glomerulosclerosis (pFSGS). However, its usefulness as a biomarker for FSGS remains controversial. We conducted a
Externí odkaz:
https://doaj.org/article/5b56bb3918b14ca4ae478f18875b6fd5
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:
Woojoong Kim, Eujin Park, Yo Han Ahn, Jiwon M. Lee, Hee Gyung Kang, Byung Joo Kim, Il-Soo Ha, Hae Il Cheong
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S5-S9 (2016)
Blau syndrome (BS) is a rare autosomal dominant, inflammatory syndrome that is characterized by the clinical triad of granulomatous dermatitis, symmetric arthritis, and recurrent uveitis. Mutations in the nucleotide oligomerization domain 2 (NOD2) ge
Externí odkaz:
https://doaj.org/article/f2fef62ccfad4550b4b0283ebf951a39
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:
Woojoong, Kim, Eujin, Park, Yo Han, Ahn, Jiwon M, Lee, Hee Gyung, Kang, Byung Joo, Kim, Il-Soo, Ha, Hae Il, Cheong
Publikováno v:
Korean Journal of Pediatrics
Blau syndrome (BS) is a rare autosomal dominant, inflammatory syndrome that is characterized by the clinical triad of granulomatous dermatitis, symmetric arthritis, and recurrent uveitis. Mutations in the nucleotide oligomerization domain 2 (NOD2) ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a81ccf4688f20961e8b6aebf294fdd1e
https://pubmed.ncbi.nlm.nih.gov/28018435
https://pubmed.ncbi.nlm.nih.gov/28018435
Autor:
Jiwon M, Lee, Young Seo, Park, Joo Hoon, Lee, Se Jin, Park, Jae Il, Shin, Yong-Hoon, Park, Kee Hwan, Yoo, Min Hyun, Cho, Su-Young, Kim, Seong Heon, Kim, Mee Kyung, Namgoong, Seung Joo, Lee, Jun Ho, Lee, Hee Yeon, Cho, Kyoung Hee, Han, Hee Gyung, Kang, Il Soo, Ha, Jun-Seok, Bae, Nayoung K D, Kim, Woong-Yang, Park, Hae Il, Cheong
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 57(3)
Atypical hemolytic uremic syndrome (aHUS) is a rare disease with a genetic predisposition. Few studies have evaluated the disease in the Asian population. We studied a Korean pediatric cohort to delineate the clinical characteristics and genotypes.A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d92a9012f5b1281bf088b6e2e787ea6f
https://pubmed.ncbi.nlm.nih.gov/25443527
https://pubmed.ncbi.nlm.nih.gov/25443527
Autor:
Woojoong Kim, Eujin Park, Yo Han Ahn, Jiwon M. Lee, Hee Gyung Kang, Byung Joo Kim, Il-Soo Ha, Hae Il Cheong
Publikováno v:
Korean Journal of Pediatrics; 2016, Vol. 59 Issue Suppl1, pS5-S9, 5p