Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

1,587 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
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: han kh. 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.
Variable renal phenotype in a family with an INF2 mutation.
Lee HK, Han KH, Jung YH, Kang HG, Moon KC, Ha IS, Choi Y, Cheong HI. Lee HK, et al. Among authors: han kh. Pediatr Nephrol. 2011 Jan;26(1):73-6. doi: 10.1007/s00467-010-1644-5. Epub 2010 Aug 28. Pediatr Nephrol. 2011. PMID: 20803156
A case of systemic amyloidosis associated with cyclic neutropenia.
Lee H, Han KH, Jung YH, Kang HG, Moon KC, Ha IS, Choi Y, Cheong HI. Lee H, et al. Among authors: han kh. Pediatr Nephrol. 2011 Apr;26(4):625-9. doi: 10.1007/s00467-010-1715-7. Epub 2010 Dec 15. Pediatr Nephrol. 2011. PMID: 21161286
Renal manifestations of patients with MYH9-related disorders.
Han KH, Lee H, Kang HG, Moon KC, Lee JH, Park YS, Ha IS, Ahn HS, Choi Y, Cheong HI. Han KH, et al. Pediatr Nephrol. 2011 Apr;26(4):549-55. doi: 10.1007/s00467-010-1735-3. Epub 2011 Jan 6. Pediatr Nephrol. 2011. PMID: 21210153
Genetic basis of Bartter syndrome in Korea.
Lee BH, Cho HY, Lee H, Han KH, Kang HG, Ha IS, Lee JH, Park YS, Shin JI, Lee DY, Kim SY, Choi Y, Cheong HI. Lee BH, et al. Among authors: han kh. Nephrol Dial Transplant. 2012 Apr;27(4):1516-21. doi: 10.1093/ndt/gfr475. Epub 2011 Aug 23. Nephrol Dial Transplant. 2012. PMID: 21865213
Urinary exosomal WT1 in childhood nephrotic syndrome.
Lee H, Han KH, Lee SE, Kim SH, Kang HG, Cheong HI. Lee H, et al. Among authors: han kh. Pediatr Nephrol. 2012 Feb;27(2):317-20. doi: 10.1007/s00467-011-2035-2. Epub 2011 Nov 11. Pediatr Nephrol. 2012. PMID: 22076591
Genetic basis of congenital and infantile nephrotic syndromes.
Lee JH, Han KH, Lee H, Kang HG, Moon KC, Shin JI, Hahn H, Park YS, Pai KS, Cho BS, Kim SY, Lee SJ, Ha IS, Choi Y, Cheong HI. Lee JH, et al. Among authors: han kh. Am J Kidney Dis. 2011 Dec;58(6):1042-3. doi: 10.1053/j.ajkd.2011.09.007. Am J Kidney Dis. 2011. PMID: 22099579 No abstract available.
1,587 results