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Page 1
Clinical characteristics and outcomes of immune-complex membranoproliferative glomerulonephritis and C3 glomerulopathy in Japanese children.
Ueda C, Horinouchi T, Inoki Y, Ichikawa Y, Tanaka Y, Kitakado H, Kondo A, Sakakibara N, Nagano C, Yamamura T, Fujimura J, Kamiyoshi N, Ishimori S, Ninchoji T, Kaito H, Shima Y, Iijima K, Nozu K, Yoshikawa N. Ueda C, et al. Among authors: sakakibara n. Pediatr Nephrol. 2024 Apr 25. doi: 10.1007/s00467-024-06377-7. Online ahead of print. Pediatr Nephrol. 2024. PMID: 38662234
Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch-Schönlein purpura nephritis of moderate severity.
Nagai S, Horinouchi T, Ninchoji T, Kondo A, Aoto Y, Ishiko S, Sakakibara N, Nagano C, Yamamura T, Kaito H, Tanaka R, Shima Y, Fujimura J, Kamiyoshi N, Ishimori S, Nakanishi K, Yoshikawa N, Iijima K, Nozu K. Nagai S, et al. Among authors: sakakibara n. Pediatr Nephrol. 2022 Aug;37(8):1845-1853. doi: 10.1007/s00467-021-05395-z. Epub 2022 Jan 11. Pediatr Nephrol. 2022. PMID: 35015121
Clinical and pathological investigation of oligomeganephronia.
Kitakado H, Horinouchi T, Masuda C, Kondo A, Nagai S, Aoto Y, Sakakibara N, Ninchoji T, Yoshikawa N, Nozu K. Kitakado H, et al. Among authors: sakakibara n. Pediatr Nephrol. 2023 Mar;38(3):757-762. doi: 10.1007/s00467-022-05687-y. Epub 2022 Jul 21. Pediatr Nephrol. 2023. PMID: 35861872
Long-term outcome of combination therapy with corticosteroids, mizoribine and RAS inhibitors as initial therapy for severe childhood IgA vasculitis with nephritis.
Nagai S, Horinouchi T, Ninchoji T, Ichikawa Y, Tanaka Y, Kitakado H, Ueda C, Kondo A, Aoto Y, Sakakibara N, Kaito H, Tanaka R, Shima Y, Fujimura J, Kamiyoshi N, Ishimori S, Nakanishi K, Yoshikawa N, Iijima K, Nozu K. Nagai S, et al. Among authors: sakakibara n. Pediatr Nephrol. 2023 Dec;38(12):4023-4031. doi: 10.1007/s00467-023-06052-3. Epub 2023 Jun 29. Pediatr Nephrol. 2023. PMID: 37380934
Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene.
Nakanishi K, Okamoto T, Nozu K, Hara S, Sato Y, Hayashi A, Takahashi T, Nagano C, Sakakibara N, Horinouchi T, Fujimura J, Minamikawa S, Yamamura T, Rossanti R, Nagase H, Kaito H, Ariga T, Iijima K. Nakanishi K, et al. Among authors: sakakibara n. Clin Exp Nephrol. 2019 May;23(5):669-675. doi: 10.1007/s10157-018-1682-z. Epub 2018 Dec 24. Clin Exp Nephrol. 2019. PMID: 30584653
Clinical characteristics of HNF1B-related disorders in a Japanese population.
Nagano C, Morisada N, Nozu K, Kamei K, Tanaka R, Kanda S, Shiona S, Araki Y, Ohara S, Matsumura C, Kasahara K, Mori Y, Seo A, Miura K, Washiyama M, Sugimoto K, Harada R, Tazoe S, Kourakata H, Enseki M, Aotani D, Yamada T, Sakakibara N, Yamamura T, Minamikawa S, Ishikura K, Ito S, Hattori M, Iijima K. Nagano C, et al. Among authors: sakakibara n. Clin Exp Nephrol. 2019 Sep;23(9):1119-1129. doi: 10.1007/s10157-019-01747-0. Epub 2019 May 27. Clin Exp Nephrol. 2019. PMID: 31131422
Comprehensive genetic diagnosis of Japanese patients with severe proteinuria.
Nagano C, Yamamura T, Horinouchi T, Aoto Y, Ishiko S, Sakakibara N, Shima Y, Nakanishi K, Nagase H, Iijima K, Nozu K. Nagano C, et al. Among authors: sakakibara n. Sci Rep. 2020 Jan 14;10(1):270. doi: 10.1038/s41598-019-57149-5. Sci Rep. 2020. PMID: 31937884 Free PMC article.
Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1.
Inoue T, Nagano C, Matsuo M, Yamamura T, Sakakibara N, Horinouchi T, Shibagaki Y, Ichikawa D, Aoto Y, Ishiko S, Ishimori S, Rossanti R, Iijima K, Nozu K. Inoue T, et al. Among authors: sakakibara n. Clin Exp Nephrol. 2020 Jul;24(7):606-612. doi: 10.1007/s10157-020-01876-x. Epub 2020 Mar 22. Clin Exp Nephrol. 2020. PMID: 32201916 Free PMC article.
Clinical and genetic variability of PAX2-related disorder in the Japanese population.
Rossanti R, Morisada N, Nozu K, Kamei K, Horinouchi T, Yamamura T, Minamikawa S, Fujimura J, Nagano C, Sakakibara N, Ninchoji T, Kaito H, Ito S, Tanaka R, Iijima K. Rossanti R, et al. Among authors: sakakibara n. J Hum Genet. 2020 Jun;65(6):541-549. doi: 10.1038/s10038-020-0741-y. Epub 2020 Mar 16. J Hum Genet. 2020. PMID: 32203253
370 results