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635 results

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Page 1
Genotype-phenotype correlations in children with Gitelman syndrome.
Cho MH, Park PG, Kim JH, Jang KM, Lee JM, Yang EM, Park SJ, Suh JS, Cho H, Lee JW, Lee JH, Koo JW, Namgoong MK, Kim KH, Ahn YH, Kang HG, Cheong HI. Cho MH, et al. Among authors: ahn yh. Clin Exp Nephrol. 2024 Mar 13. doi: 10.1007/s10157-024-02474-x. Online ahead of print. Clin Exp Nephrol. 2024. PMID: 38478191
Longitudinal progression trajectory of estimated glomerular filtration rate in children with chronic kidney disease: results from the KNOW-Ped CKD (KoreaN cohort study for Outcomes in patients With Pediatric Chronic Kidney Disease).
Yang EM, Kim J, Park E, Han KH, Kim SH, Cho H, Shin JI, Cho MH, Lee JH, Kim JH, Kang HG, Ha IS, Ahn YH. Yang EM, et al. Among authors: ahn yh. Kidney Res Clin Pract. 2024 Feb 23. doi: 10.23876/j.krcp.23.198. Online ahead of print. Kidney Res Clin Pract. 2024. PMID: 38389150 Free article.
Early Sepsis-Associated Acute Kidney Injury and Obesity.
Ahn YH, Yoon SM, Lee J, Lee SM, Oh DK, Lee SY, Park MH, Lim CM, Lee HY; Korean Sepsis Alliance Investigators. Ahn YH, et al. JAMA Netw Open. 2024 Feb 5;7(2):e2354923. doi: 10.1001/jamanetworkopen.2023.54923. JAMA Netw Open. 2024. PMID: 38319660 Free PMC article.
Outcome of immunosuppression in children with IgA vasculitis-related nephritis.
Rohner K, Marlais M, Ahn YH, Ali A, Alsharief A, Novak AB, Brambilla M, Cakici EK, Candan C, Canpolat N, Yu-Hin Chan E, Decramer S, Didsbury M, Durao F, Durkan AM, Düzova A, Forbes T, Gracchi V, Güngör T, Horinouchi T, Demir BK, Kobayashi Y, Koskela M, Kurt-Sukur ED, La Scola C, Langan D, Li X, Malgieri G, Mastrangelo A, Min J, Mizerska-Wasiak M, Moussaoui N, Noyan A, Nuutinen M, O'Gormon J, Okamoto T, Oni L, Oosterveld M, Pańczyk-Tomaszewska M, Parmaksiz G, Pasini A, Rianthavorn P, Roelofs J, Shen Y, Sinha R, Topaloglu R, Torres DD, Udagawa T, Wennerström M, Yap YC, Tullus K. Rohner K, et al. Among authors: ahn yh. Nephrol Dial Transplant. 2024 Jan 11:gfae009. doi: 10.1093/ndt/gfae009. Online ahead of print. Nephrol Dial Transplant. 2024. PMID: 38211969
Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract.
Kołbuc M, Kołek MF, Motyka R, Bieniaś B, Habbig S, Burgmaier K, Prikhodina L, Papizh S, Tasic V, Okorn C, Szczepańska M, Kiliś-Pstrusińska K, Wasilewska A, Adamczyk P, Tkaczyk M, Pańczyk-Tomaszewska M, Miklaszewska M, Pawlaczyk K, Bukowska-Olech E, Jamsheer A, Jankauskiene A, König J, Cheong HI, Ahn YH, Kaspar S, Sikora P, Beck BB, Zaniew M. Kołbuc M, et al. Among authors: ahn yh. Pediatr Nephrol. 2024 Jun;39(6):1847-1858. doi: 10.1007/s00467-023-06262-9. Epub 2024 Jan 10. Pediatr Nephrol. 2024. PMID: 38196016 Free PMC article. Clinical Trial.
635 results