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Genotype and Phenotype Analysis in Pediatric Patients with Cystinuria.
Kim JH, Park E, Hyun HS, Lee BH, Kim GH, Lee JH, Park YS, Kang HG, Ha IS, Cheong HI. Kim JH, et al. Among authors: kim gh. J Korean Med Sci. 2017 Feb;32(2):310-314. doi: 10.3346/jkms.2017.32.2.310. J Korean Med Sci. 2017. PMID: 28049243 Free PMC article.
Reninoma: a rare cause of curable hypertension.
Kim JH, Kim JH, Cho MH, Park E, Hyun HS, Ahn YH, Kang HG, Moon KC, Ha IS, Cheong HI. Kim JH, et al. Korean J Pediatr. 2019 Apr;62(4):144-147. doi: 10.3345/kjp.2018.06926. Epub 2018 Oct 29. Korean J Pediatr. 2019. PMID: 30376707 Free PMC article.
Urological Problems in Patients with Menkes Disease.
Kim MY, Kim JH, Cho MH, Choi YH, Kim SH, Im YJ, Park K, Kang HG, Chae JH, Cheong HI. Kim MY, et al. Among authors: kim sh, kim jh. J Korean Med Sci. 2018 Dec 26;34(1):e4. doi: 10.3346/jkms.2019.34.e4. eCollection 2019 Jan 7. J Korean Med Sci. 2018. PMID: 30618512 Free PMC article.
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome.
Jia X, Yamamura T, Gbadegesin R, McNulty MT, Song K, Nagano C, Hitomi Y, Lee D, Aiba Y, Khor SS, Ueno K, Kawai Y, Nagasaki M, Noiri E, Horinouchi T, Kaito H, Hamada R, Okamoto T, Kamei K, Kaku Y, Fujimaru R, Tanaka R, Shima Y; Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan; Baek J, Kang HG, Ha IS, Han KH, Yang EM; Korean Consortium of Hereditary Renal Diseases in Children; Abeyagunawardena A, Lane B, Chryst-Stangl M, Esezobor C, Solarin A; Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group); Dossier C, Deschênes G; NEPHROVIR; Vivarelli M, Debiec H, Ishikura K, Matsuo M, Nozu K, Ronco P, Cheong HI, Sampson MG, Tokunaga K, Iijima K. Jia X, et al. Kidney Int. 2020 Nov;98(5):1308-1322. doi: 10.1016/j.kint.2020.05.029. Epub 2020 Jun 14. Kidney Int. 2020. PMID: 32554042 Free PMC article.
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