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Page 1
Spontaneous regression of arterial pseudoaneurysm after kidney biopsy.
Yoshimoto H, Ninchoji T, Nagai S, Horinouchi T, Nozu K. Yoshimoto H, et al. Among authors: ninchoji t. CEN Case Rep. 2022 Feb;11(1):159-160. doi: 10.1007/s13730-021-00615-9. Epub 2021 Jun 18. CEN Case Rep. 2022. PMID: 34143383 Free PMC article. No abstract available.
FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child.
Rossanti R, Watanabe T, Nagano C, Hara S, Horinouchi T, Yamamura T, Sakakibara N, Ninchoji T, Iijima K, Nozu K. Rossanti R, et al. Among authors: ninchoji t. CEN Case Rep. 2021 Feb;10(1):100-105. doi: 10.1007/s13730-020-00529-y. Epub 2020 Sep 9. CEN Case Rep. 2021. PMID: 32902815 Free PMC article.
Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry.
Nakanishi K, Kaito H, Ogi M, Takai D, Fujimura J, Horinouchi T, Yamamura T, Minamikawa S, Ninchoji T, Nozu K, Imadome KI, Iijima K. Nakanishi K, et al. Among authors: ninchoji t. Case Rep Nephrol Dial. 2018 Sep 25;8(3):198-206. doi: 10.1159/000493092. eCollection 2018 Sep-Dec. Case Rep Nephrol Dial. 2018. PMID: 30397600 Free PMC article.
Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases.
Kondo A, Nagano C, Ishiko S, Omori T, Aoto Y, Rossanti R, Sakakibara N, Horinouchi T, Yamamura T, Nagai S, Okada E, Shima Y, Nakanishi K, Ninchoji T, Kaito H, Takeda H, Nagase H, Morisada N, Iijima K, Nozu K. Kondo A, et al. Among authors: ninchoji t. Sci Rep. 2021 Aug 9;11(1):16099. doi: 10.1038/s41598-021-95521-6. Sci Rep. 2021. PMID: 34373523 Free PMC article.
Efficacy of combination therapy for childhood complicated focal IgA nephropathy.
Aoto Y, Ninchoji T, Kaito H, Shima Y, Fujimura J, Kamiyoshi N, Ishimori S, Nakanishi K, Minamikawa S, Ishiko S, Sakakibara N, Nagano C, Horinouchi T, Yamamura T, Nagai S, Kondo A, Inaguma Y, Tanaka R, Yoshikawa N, Iijima K, Nozu K. Aoto Y, et al. Among authors: ninchoji t. Clin Exp Nephrol. 2022 Jun;26(6):561-570. doi: 10.1007/s10157-022-02190-4. Epub 2022 Feb 9. Clin Exp Nephrol. 2022. PMID: 35138499
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: ninchoji t. 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
The utility of urinary CD80 as a diagnostic marker in patients with renal diseases.
Minamikawa S, Nozu K, Maeta S, Yamamura T, Nakanishi K, Fujimura J, Horinouchi T, Nagano C, Sakakibara N, Nagase H, Shima H, Noda K, Ninchoji T, Kaito H, Iijima K. Minamikawa S, et al. Among authors: ninchoji t. Sci Rep. 2018 Nov 23;8(1):17322. doi: 10.1038/s41598-018-35798-2. Sci Rep. 2018. PMID: 30470792 Free PMC article.
107 results