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Different Clinical Courses of Nephronophthisis in Dizygotic Twins.
Oki Y, Katsuma A, Okabe M, Watanabe M, Sagasaki M, Takahashi D, Kimura A, Kato J, Ueda H, Hataya H, Fujimaru T, Mori T, Sohara E, Uchida S, Miyazaki Y, Yokoo T. Oki Y, et al. Among authors: uchida s. Intern Med. 2023 Jan 1;62(1):87-90. doi: 10.2169/internalmedicine.8707-21. Epub 2022 Jun 7. Intern Med. 2023. PMID: 35676033 Free PMC article.
Genetic Background and Clinicopathologic Features of Adult-onset Nephronophthisis.
Fujimaru T, Kawanishi K, Mori T, Mishima E, Sekine A, Chiga M, Mizui M, Sato N, Yanagita M, Ooki Y, Nagahama K, Ohnuki Y, Hamano N, Watanabe S, Mochizuki T, Nagatsuji K, Tanaka K, Tsukamoto T, Tsushima H, Shimamoto M, Tsuji T, Kuyama T, Kawamoto S, Maki K, Katsuma A, Oishi M, Yamamoto K, Mandai S, Kikuchi H, Ando F, Mori Y, Susa K, Iimori S, Naito S, Rai T, Hoshino J, Ubara Y, Miyazaki M, Nagata M, Uchida S, Sohara E. Fujimaru T, et al. Among authors: uchida s. Kidney Int Rep. 2021 Mar 4;6(5):1346-1354. doi: 10.1016/j.ekir.2021.02.005. eCollection 2021 May. Kidney Int Rep. 2021. PMID: 34013113 Free PMC article.
Two Cases of Hemodialysis-associated Chronic Portal-systemic Shunt Encephalopathy (CPSE) with Opposite Changes in the Blood Ammonia Concentrations during Hemodialysis: A Case Report and Literature Review.
Oi K, Okado T, Togo H, Iimori S, Yui N, Sohara E, Kanda E, Rai T, Sasaki S, Uchida S. Oi K, et al. Among authors: uchida s. Intern Med. 2015;54(11):1375-80. doi: 10.2169/internalmedicine.54.3488. Epub 2015 Jun 1. Intern Med. 2015. PMID: 26027990 Free article. Review.
Severe Osteomalacia with Dent Disease Caused by a Novel Intronic Mutation of the CLCN5 gene.
Matsumoto A, Matsui I, Mori T, Sakaguchi Y, Mizui M, Ueda Y, Takahashi A, Doi Y, Shimada K, Yamaguchi S, Kubota K, Hashimoto N, Oka T, Takabatake Y, Sohara E, Hamano T, Uchida S, Isaka Y. Matsumoto A, et al. Among authors: uchida s. Intern Med. 2018 Dec 15;57(24):3603-3610. doi: 10.2169/internalmedicine.1272-18. Epub 2018 Aug 10. Intern Med. 2018. PMID: 30101934 Free PMC article.
Echocardiographic Findings and Genotypes in Autosomal Dominant Polycystic Kidney Disease.
Miyamoto R, Sekine A, Fujimaru T, Suwabe T, Mizuno H, Hasegawa E, Yamanouchi M, Chiga M, Mori T, Sohara E, Uchida S, Sawa N, Ubara Y, Hoshino J. Miyamoto R, et al. Among authors: uchida s. Kidney Dis (Basel). 2021 Nov 26;8(3):246-252. doi: 10.1159/000520300. eCollection 2022 May. Kidney Dis (Basel). 2021. PMID: 35702705 Free PMC article.
2,461 results