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Page 1
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
Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.
Kamiyoshi N, Nozu K, Urahama Y, Matsunoshita N, Yamamura T, Minamikawa S, Ninchoji T, Morisada N, Nakanishi K, Kaito H, Iijima K. Kamiyoshi N, et al. Among authors: ninchoji t. Clin Exp Nephrol. 2016 Apr;20(2):253-7. doi: 10.1007/s10157-015-1160-9. Epub 2015 Sep 1. Clin Exp Nephrol. 2016. PMID: 26323216
Female X-linked Alport syndrome with somatic mosaicism.
Yokota K, Nozu K, Minamikawa S, Yamamura T, Nakanishi K, Kaneda H, Hamada R, Nozu Y, Shono A, Ninchoji T, Morisada N, Ishimori S, Fujimura J, Horinouchi T, Kaito H, Nakanishi K, Morioka I, Taniguchi-Ikeda M, Iijima K. Yokota K, et al. Among authors: ninchoji t. Clin Exp Nephrol. 2017 Oct;21(5):877-883. doi: 10.1007/s10157-016-1352-y. Epub 2016 Oct 31. Clin Exp Nephrol. 2017. PMID: 27796712
An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis.
Yamamura T, Nozu K, Miyoshi Y, Nakanishi K, Fujimura J, Horinouchi T, Minamikawa S, Mori N, Fujimaru R, Nakanishi K, Ninchoji T, Kaito H, Mariko TI, Morioka I, Matsuo M, Iijima K. Yamamura T, et al. Among authors: ninchoji t. BMC Nephrol. 2017 Dec 4;18(1):353. doi: 10.1186/s12882-017-0774-4. BMC Nephrol. 2017. PMID: 29202719 Free PMC article.
X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assay.
Rossanti R, Nozu K, Fukunaga A, Nagano C, Horinouchi T, Yamamura T, Sakakibara N, Minamikawa S, Ishiko S, Aoto Y, Okada E, Ninchoji T, Kato N, Maruyama S, Kono K, Nishi S, Iijima K, Fujii H. Rossanti R, et al. Among authors: ninchoji t. Clin Exp Nephrol. 2021 Nov;25(11):1224-1230. doi: 10.1007/s10157-021-02099-4. Epub 2021 Jun 14. Clin Exp Nephrol. 2021. PMID: 34128148
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes.
Ishiko S, Morisada N, Kondo A, Nagai S, Aoto Y, Okada E, Rossanti R, Sakakibara N, Nagano C, Horinouchi T, Yamamura T, Ninchoji T, Kaito H, Hamada R, Shima Y, Nakanishi K, Matsuo M, Iijima K, Nozu K. Ishiko S, et al. Among authors: ninchoji t. Clin Exp Nephrol. 2022 Feb;26(2):140-153. doi: 10.1007/s10157-021-02135-3. Epub 2021 Sep 18. Clin Exp Nephrol. 2022. PMID: 34536170 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
Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndrome.
Ishiko S, Tanaka A, Takeda A, Hara M, Hamano N, Koizumi M, Ueno T, Hayashi H, Kondo A, Nagai S, Aoto Y, Sakakibara N, Nagano C, Horinouchi T, Yamamura T, Ninchoji T, Shima Y, Nakanishi K, Yoshikawa N, Iijima K, Nozu K. Ishiko S, et al. Among authors: ninchoji t. Clin Exp Nephrol. 2021 Jul;25(7):779-787. doi: 10.1007/s10157-021-02054-3. Epub 2021 Mar 20. Clin Exp Nephrol. 2021. PMID: 33743099
107 results