Zobrazeno 1 - 10
of 10
pro vyhledávání: '"II-Soo Ha"'
Autor:
Yoon Ha Lee, Yong Hyuk Jeon, Seon Hee Lim, Yo Han Ahn, Sang-Yun Lee, Jung min Ko, II-Soo Ha, Hee Gyung Kang
Publikováno v:
Journal of Genetic Medicine. 18:142-146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0551fa20c3e282bce0f24c6c9bb7e04
https://doi.org/10.5734/jgm.2021.18.2.142
https://doi.org/10.5734/jgm.2021.18.2.142
Autor:
Young Hoon Cho, Jongwon Ha, Hee Gyung Kang, Yo Han Ahn, Hae Ii Cheong, Eujin Park, Sang Ii Min, Kyung Chul Moon, Hye Sun Hyun, Ii Soo Ha
Publikováno v:
Journal of Clinical Medicine
Volume 8
Issue 4
Journal of Clinical Medicine, Vol 8, Iss 4, p 491 (2019)
Volume 8
Issue 4
Journal of Clinical Medicine, Vol 8, Iss 4, p 491 (2019)
A retrospective review was performed to assess the risk factors and outcomes of BK virus infection and nephropathy (BKVN), an early complication in pediatric kidney allograft recipients. The study investigated the incidence, risk factors, and clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e09b576173fecbb92b1b5607a8d3c2f
Autor:
Ii Soo Ha, Jiwon Lee, Young Seo Park, Eujin Park, Woong-Yang Park, Yo Han Ahn, Hee Gyung Kang, Hae Ii Cheong, Joo Hoon Lee, Nayoung K.D. Kim
Publikováno v:
Pediatric Nephrology. 31:113-119
Hepatorenal fibrocystic diseases (HRFCDs) are a group of monogenic disorders characterized by developmental abnormalities involving the liver and kidney. In this study, we performed genotype and phenotype analyses of children with HRFCDs to determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97c0235b70a352b3e3d010b4891cb342
https://doi.org/10.1007/s00467-015-3185-4
https://doi.org/10.1007/s00467-015-3185-4
Autor:
Hee Gyung Kang, Jun Seok Bae, Ii Soo Ha, Yo Han Ahn, Nayoung K.D. Kim, Jiwon Lee, Young Seo Park, Joo Hoon Lee, Kyoung Bun Lee, Hae I.I. Cheong, Woong-Yang Park, Kyung Chul Moon, Yong Mee Cho
Publikováno v:
Pediatric Nephrology. 30:1451-1458
Nephronophthisis 13 (NPHP 13) is associated with mutations in the WDR19 gene, which encodes for a protein in the intraflagellar transport complex. Herein, we describe six additional cases accompanied by Caroli syndrome or disease.Targeted exome seque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3291d900287216f096d8b320b30d54cf
https://doi.org/10.1007/s00467-015-3068-8
https://doi.org/10.1007/s00467-015-3068-8
Publikováno v:
Journal of Clinical Medicine
Volume 8
Issue 2
Journal of Clinical Medicine, Vol 8, Iss 2, p 178 (2019)
Volume 8
Issue 2
Journal of Clinical Medicine, Vol 8, Iss 2, p 178 (2019)
Alport syndrome (AS) is one of the most frequent hereditary nephritis leading to end-stage renal disease (ESRD). Although X-linked (XLAS) inheritance is the most common form, cases with autosomal recessive inheritance with mutations in COL4A3 or COL4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea87dee767d6165d196959e0f5d8b506
https://hdl.handle.net/20.500.14094/90005681
https://hdl.handle.net/20.500.14094/90005681
Autor:
Kyoung Hee Han, Hee Gyung Kang, Hyun Kyung Lee, Yun Hye Jung, Ii Soo Ha, Yun Shik Choi, Se Eun Lee, Cheong Hi
Publikováno v:
Pediatric Nephrology. 25:1779-2004
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d92eacc953c26b2794e0ff5dc746cdbb
https://doi.org/10.1007/s00467-010-1577-z
https://doi.org/10.1007/s00467-010-1577-z
Autor:
Hye Won Park, Hae Ii Cheong, Kyu Sup Han, Yong Choi, Hye Won Han, Ii Soo Ha, Sang Joon Kim, Hyun Lee
Publikováno v:
Nephrology Dialysis Transplantation. 15:78-81
It is a worrisome complication for paediatric nephroBackground. We analysed risk factors to predict the logists because of its high rate of incidence, the recurrence of nephrotic syndrome and the therapeutic subsequent graft loss, and inability to pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97dc7b2c0525b5c5f5e533e9b5ef8fb0
https://doi.org/10.1093/ndt/15.1.78
https://doi.org/10.1093/ndt/15.1.78
Autor:
Yong Choi, Ii Soo Ha, Hae Ii Cheong, Jung Sue Kim, Yong Seung Hwang, Jong Hee Chae, Hye Won Park, Hyun Soon Lee
Publikováno v:
Pediatric Nephrology. 13:477-480
Several cases of hereditary glomerulopathy associated with an A to G transition at position 3243 in mitochondrial DNA, which is known to be associated with most cases of MELAS syndrome (myopathy, encephalopathy, lactic acidosis, and stroke-like episo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38a1676cbde3dc7bc7031cae33220f6a
https://doi.org/10.1007/s004670050641
https://doi.org/10.1007/s004670050641
Autor:
Byung Joo Kim, Ii Soo Ha, Hae Ii Cheong, Hee Gyung Kang, Woojoong， Kim, Eujin Park, Yo Han Ahn, Ji Won Lee
Publikováno v:
Korean Journal of Pediatrics. 59:S5
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=doi_________::464d74e1acd3682e192d21f4ef2e96d5
https://doi.org/10.3345/kjp.2016.59.11.s5
https://doi.org/10.3345/kjp.2016.59.11.s5
Autor:
Hye Jin Chang, Kyoung Hee Han, Min Hyun Cho, Young Seo Park, Hee Gyung Kang, Hae II Cheong, II Soo Ha
Publikováno v:
Korean Journal of Pediatrics; Mar2014, Vol. 57 Issue 3, p135-139, 5p