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Page 1
Protocol for the nationwide registry of patients with polycystic kidney disease: japanese national registry of PKD (JRP).
Nakatani S, Kawano H, Sato M, Hoshino J, Nishio S, Miura K, Sekine A, Suwabe T, Hidaka S, Kataoka H, Ishikawa E, Shimazu K, Uchiyama K, Fujimaru T, Moriyama T, Kurashige M, Shimabukuro W, Hattanda F, Kimura T, Ushio Y, Manabe S, Watanabe H, Mitobe M, Seta K, Shimada Y, Kai H, Katayama K, Ichikawa D, Hayashi H, Hanaoka K, Mochizuki T, Nakanishi K, Tsuchiya K, Horie S, Isaka Y, Muto S; JRP collaborators. Nakatani S, et al. Clin Exp Nephrol. 2024 Oct;28(10):1004-1015. doi: 10.1007/s10157-024-02509-3. Epub 2024 May 11. Clin Exp Nephrol. 2024. PMID: 38734869
Association between maternally inherited deafness, epilepsy, and intellectual disability and the m.12207G > A MT-TS2 pathogenic variant in a Japanese family.
Suzuki-Ajihara S, Saito-Tsuruoka M, Harashima H, Arai K, Koide H, Yatsuka Y, Imai-Okazaki A, Okazaki Y, Murayama K, Numakura C, Akioka Y, Ohtake A. Suzuki-Ajihara S, et al. Among authors: akioka y. Mol Genet Metab Rep. 2023 Mar 17;35:100966. doi: 10.1016/j.ymgmr.2023.100966. eCollection 2023 Jun. Mol Genet Metab Rep. 2023. PMID: 36967720 Free PMC article.
Precise clinicopathologic findings for application of genetic testing in pediatric kidney transplant recipients with focal segmental glomerulosclerosis/steroid-resistant nephrotic syndrome.
Miura K, Kaneko N, Hashimoto T, Ishizuka K, Shirai Y, Hisano M, Chikamoto H, Akioka Y, Kanda S, Harita Y, Yamamoto T, Hattori M. Miura K, et al. Among authors: akioka y. Pediatr Nephrol. 2023 Feb;38(2):417-429. doi: 10.1007/s00467-022-05604-3. Epub 2022 Jun 2. Pediatr Nephrol. 2023. PMID: 35655039
Laminin β2 variants associated with isolated nephropathy that impact matrix regulation.
Kikkawa Y, Hashimoto T, Takizawa K, Urae S, Masuda H, Matsunuma M, Yamada Y, Hamada K, Nomizu M, Liapis H, Hisano M, Akioka Y, Miura K, Hattori M, Miner JH, Harita Y. Kikkawa Y, et al. Among authors: akioka y. JCI Insight. 2021 Mar 22;6(6):e145908. doi: 10.1172/jci.insight.145908. JCI Insight. 2021. PMID: 33749661 Free PMC article.
Amount and selectivity of proteinuria may predict the treatment response in post-transplant recurrence of focal segmental glomerulosclerosis: a single-center retrospective study.
Ban H, Miura K, Kaneko N, Shirai Y, Yabuuchi T, Ishizuka K, Chikamoto H, Akioka Y, Shimizu S, Ishida H, Tanabe K, Hattori M. Ban H, et al. Among authors: akioka y. Pediatr Nephrol. 2021 Aug;36(8):2433-2442. doi: 10.1007/s00467-021-04951-x. Epub 2021 Feb 4. Pediatr Nephrol. 2021. PMID: 33538912
Renal hypoplasia can be the cause of membranous nephropathy-like lesions.
Takizawa K, Miura K, Kaneko N, Yabuuchi T, Ishizuka K, Kanda S, Harita Y, Akioka Y, Horita S, Taneda S, Honda K, Hattori M. Takizawa K, et al. Among authors: akioka y. Clin Exp Nephrol. 2020 Sep;24(9):813-820. doi: 10.1007/s10157-020-01902-y. Epub 2020 May 19. Clin Exp Nephrol. 2020. PMID: 32424448
Individualized concept for the treatment of autosomal recessive polycystic kidney disease with end-stage renal disease.
Miura K, Sato Y, Yabuuchi T, Kaneko N, Ishizuka K, Chikamoto H, Akioka Y, Nawashiro Y, Hisano M, Imamura H, Miyai T, Sakamoto S, Kasahara M, Fuchinoue S, Okumi M, Ishida H, Tanabe K, Hattori M. Miura K, et al. Among authors: akioka y. Pediatr Transplant. 2020 May;24(3):e13690. doi: 10.1111/petr.13690. Epub 2020 Mar 3. Pediatr Transplant. 2020. PMID: 32128974
65 results