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Diagnostic strategy for inherited hypomagnesemia.
Horinouchi T, Nozu K, Kamiyoshi N, Kamei K, Togawa H, Shima Y, Urahama Y, Yamamura T, Minamikawa S, Nakanishi K, Fujimura J, Morioka I, Ninchoji T, Kaito H, Nakanishi K, Iijima K. Horinouchi T, et al. Among authors: morioka i. Clin Exp Nephrol. 2017 Dec;21(6):1003-1010. doi: 10.1007/s10157-017-1396-7. Epub 2017 Mar 1. Clin Exp Nephrol. 2017. PMID: 28251383
A surviving case of papillorenal syndrome with the phenotype of Potter sequence.
Fujioka K, Morioka I, Nozu K, Nishimoto M, Amano M, Tagami M, Honda S, Yokoyama N, Yamada H, Iijima K, Matsuo M. Fujioka K, et al. Among authors: morioka i. Pediatr Int. 2011 Jun;53(3):406-8. doi: 10.1111/j.1442-200X.2010.03261.x. Pediatr Int. 2011. PMID: 21696512 No abstract available.
Novel treatment strategy for Japanese newborns with high serum unbound bilirubin.
Yokota T, Morioka I, Kodera T, Morisawa T, Sato I, Kawano S, Koda T, Matsuo K, Fujioka K, Morikawa S, Miwa A, Shibata A, Yokoyama N, Yonetani M, Yamada H, Nakamura H, Iijima K. Yokota T, et al. Among authors: morioka i. Pediatr Int. 2013 Feb;55(1):54-9. doi: 10.1111/j.1442-200X.2012.03726.x. Epub 2012 Dec 11. Pediatr Int. 2013. PMID: 22978498 Clinical Trial.
Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method.
Hashimoto F, Nishiumi S, Miyake O, Takeichi H, Chitose M, Ohtsubo H, Ishimori S, Ninchoji T, Hashimura Y, Kaito H, Morisada N, Morioka I, Fukuoka H, Yoshida M, Iijima K. Hashimoto F, et al. Among authors: morioka i. Early Hum Dev. 2013 May;89(5):315-20. doi: 10.1016/j.earlhumdev.2012.10.010. Epub 2012 Nov 22. Early Hum Dev. 2013. PMID: 23178109
418 results