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Page 1
Plasma S100A12 levels and peripheral arterial disease in end-stage renal disease.
Shiotsu Y, Mori Y, Hatta T, Maki N, Iida K, Matsuoka E, Kado H, Ishida R, Kishimoto N, Tamagaki K, Nishimura M, Iwamoto N, Ono T, Matsubara H, Kosaki A. Shiotsu Y, et al. Among authors: ishida r. Nephron Extra. 2011 Jan;1(1):242-50. doi: 10.1159/000335198. Epub 2011 Dec 21. Nephron Extra. 2011. PMID: 22470398 Free PMC article.
A Japanese Family Suffering from Familial Juvenile Hyperuricemic Nephropathy due to a Rare Mutation of the Uromodulin Gene.
Nakayama M, Mori Y, Ota N, Ishida M, Shiotsu Y, Matsuoka E, Kado H, Ishida R, Nakata M, Kitani T, Tamagaki K, Sekita C, Taniguchi A. Nakayama M, et al. Among authors: ishida m, ishida r. Case Rep Nephrol Urol. 2012 Jan;2(1):15-9. doi: 10.1159/000337343. Epub 2012 Mar 14. Case Rep Nephrol Urol. 2012. PMID: 23197950 Free PMC article.
[Case of Marfan syndrome with microscopic hematuria].
Takahashi K, Kusaba T, Ishida R, Nakanouchi T. Takahashi K, et al. Among authors: ishida r. Nihon Jinzo Gakkai Shi. 2011;53(8):1159-63. Nihon Jinzo Gakkai Shi. 2011. PMID: 22351994 Japanese.
[Case of an hemodialysis patient with MYH9 disorders].
Ishida R, Kusaba T, Kirita Y, Matsuoka E, Nakayama M, Uchiyama H, Kajita Y. Ishida R, et al. Nihon Jinzo Gakkai Shi. 2011;53(2):195-9. Nihon Jinzo Gakkai Shi. 2011. PMID: 21516706 Japanese.
Kidney-specific Sonoporation-mediated Gene Transfer.
Ishida R, Kami D, Kusaba T, Kirita Y, Kishida T, Mazda O, Adachi T, Gojo S. Ishida R, et al. Mol Ther. 2016 Feb;24(1):125-34. doi: 10.1038/mt.2015.171. Epub 2015 Sep 30. Mol Ther. 2016. PMID: 26419704 Free PMC article.
471 results