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A review of clinical characteristics and genetic backgrounds in Alport syndrome.
Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, Kaito H, Kanemoto K, Kobayashi A, Tanaka E, Tanaka K, Hama T, Fujimaru R, Miwa S, Yamamura T, Yamamura N, Horinouchi T, Minamikawa S, Nagata M, Iijima K. Nozu K, et al. Among authors: abe y. Clin Exp Nephrol. 2019 Feb;23(2):158-168. doi: 10.1007/s10157-018-1629-4. Epub 2018 Aug 20. Clin Exp Nephrol. 2019. PMID: 30128941 Free PMC article. Review.
A Novel Mutation in a Japanese Family with X-linked Alport Syndrome.
Abe Y, Iyoda M, Nozu K, Hibino S, Hihara K, Yamaguchi Y, Yamamura T, Minamikawa S, Iijima K, Shibata T, Itabashi K. Abe Y, et al. Intern Med. 2016;55(19):2843-2847. doi: 10.2169/internalmedicine.55.6873. Epub 2016 Oct 1. Intern Med. 2016. PMID: 27725546 Free PMC article.
Distribution of serum adiponectin isoforms in pediatric patients with steroid-sensitive nephrotic syndrome.
Tamai T, Kamijo K, Abe Y, Hibino S, Sakurai S, Watanabe S, Watanabe Y, Nimura S, Shiratori A, Takayanagi T, Watanabe T, Nakano Y, Ikeda H, Dobashi K, Nakano Y, Mizuno K, Itabashi K. Tamai T, et al. Among authors: abe y. Clin Exp Nephrol. 2021 Sep;25(9):1027-1034. doi: 10.1007/s10157-021-02085-w. Epub 2021 Jun 1. Clin Exp Nephrol. 2021. PMID: 34061287 Free PMC article.
Retrospective study of the renal function using estimated glomerular filtration rate and congenital anomalies of the kidney-urinary tract in pediatric Turner syndrome.
Izumita Y, Nishigaki S, Satoh M, Takubo N, Numakura C, Takahashi I, Soneda S, Abe Y, Kamasaki H, Ohtsu Y, Igaki J, Hasegawa Y, Nagasaki K. Izumita Y, et al. Among authors: abe y. Congenit Anom (Kyoto). 2020 Nov;60(6):175-179. doi: 10.1111/cga.12384. Epub 2020 Aug 4. Congenit Anom (Kyoto). 2020. PMID: 32638418
4,822 results