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899 results

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Page 1
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. Among authors: kang hg. 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.
Ifosfamide nephrotoxicity in pediatric cancer patients.
Lee BS, Lee JH, Kang HG, Hahn H, Lee JH, Shin HY, Ha IS, Cheong HI, Ahn HS, Choi Y. Lee BS, et al. Among authors: kang hg. Pediatr Nephrol. 2001 Oct;16(10):796-9. doi: 10.1007/s004670100658. Pediatr Nephrol. 2001. PMID: 11605785
Mineral bone disorder in children with chronic kidney disease: Data from the KNOW-Ped CKD (Korean cohort study for outcome in patients with pediatric chronic kidney disease) study.
Jung J, Lee KH, Park E, Park YS, Kang HG, Ahn YH, Ha IS, Kim SH, Cho H, Han KH, Cho MH, Choi HJ, Lee JH, Shin JI. Jung J, et al. Among authors: kang hg. Front Pediatr. 2023 Feb 17;11:994979. doi: 10.3389/fped.2023.994979. eCollection 2023. Front Pediatr. 2023. PMID: 36873652 Free PMC article.
Long-term outcome of Bartter syndrome in 54 patients: A multicenter study in Korea.
Choi N, Kim SH, Bae EH, Yang EM, Lee KH, Lee SH, Lee JH, Ahn YH, Cheong HI, Kang HG, Hyun HS, Kim JH. Choi N, et al. Among authors: kang hg. Front Med (Lausanne). 2023 Mar 13;10:1099840. doi: 10.3389/fmed.2023.1099840. eCollection 2023. Front Med (Lausanne). 2023. PMID: 36993809 Free PMC article.
Genotype-phenotype correlation of X-linked Alport syndrome observed in both genders: a multicenter study in South Korea.
Kim JH, Lim SH, Song JY, Cho MH, Hyun H, Yang EM, Lee JW, Cho MH, Park MJ, Lee JH, Jung J, Yoo KH, Jang KM, Pai KS, Suh JS, Namgoong MK, Chung WY, Kim SJ, Cho EY, Kim KM, Kim NH, Kim M, Paik JH, Kang HG, Ahn YH, Cheong HI. Kim JH, et al. Among authors: kang hg. Sci Rep. 2023 Apr 26;13(1):6827. doi: 10.1038/s41598-023-34053-7. Sci Rep. 2023. PMID: 37100867 Free PMC article.
Investigation of the current situation regarding diagnosis and treatment of Alport syndrome in Asian countries: results of survey of the Asian Paediatric Nephrology association (AsPNA) tubular and inherited working group.
Nozu K, Resontoc LPR, Hooman N, Vasudevan A, Ding J, Kang HG. Nozu K, et al. Among authors: kang hg. Clin Exp Nephrol. 2023 Sep;27(9):776-780. doi: 10.1007/s10157-023-02358-6. Epub 2023 Jun 8. Clin Exp Nephrol. 2023. PMID: 37289334 Free PMC article.
899 results