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Page 1
Saline versus balanced crystalloids for hydration post-kidney biopsy.
Tanaka Y, Horinouchi T, Inoki Y, Ichikawa Y, Ueda C, Kitakado H, Kondo A, Sakakibara N, Ishimori S, Yamamura T, Nagano C, Nozu K. Tanaka Y, et al. Among authors: yamamura t. Pediatr Nephrol. 2024 Nov 25. doi: 10.1007/s00467-024-06594-0. Online ahead of print. Pediatr Nephrol. 2024. PMID: 39585356
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: yamamura t. Pediatr Nephrol. 2024 Sep;39(9):2679-2689. doi: 10.1007/s00467-024-06377-7. Epub 2024 Apr 25. Pediatr Nephrol. 2024. PMID: 38662234 Free PMC article.
Aberrant splicing caused by exonic single nucleotide variants positioned 2nd or 3rd to the last nucleotide in the COL4A5 gene.
Okada E, Aoto Y, Horinouchi T, Yamamura T, Ichikawa Y, Tanaka Y, Ueda C, Kitakado H, Kondo A, Sakakibara N, Suzuki R, Usui J, Yamagata K, Iijima K, Nozu K. Okada E, et al. Among authors: yamamura t. Clin Exp Nephrol. 2023 Mar;27(3):218-226. doi: 10.1007/s10157-022-02294-x. Epub 2022 Nov 12. Clin Exp Nephrol. 2023. PMID: 36371577 Free PMC article.
All reported non-canonical splice site variants in GLA cause aberrant splicing.
Okada E, Horinouchi T, Yamamura T, Aoto Y, Suzuki R, Ichikawa Y, Tanaka Y, Masuda C, Kitakado H, Kondo A, Sakakibara N, Ishiko S, Nagano C, Ishimori S, Usui J, Yamagata K, Matsuo M, Nozu K. Okada E, et al. Among authors: yamamura t. Clin Exp Nephrol. 2023 Sep;27(9):737-746. doi: 10.1007/s10157-023-02361-x. Epub 2023 May 31. Clin Exp Nephrol. 2023. PMID: 37254000 Free PMC article.
Genotype and X-chromosome inactivation are associated with disease severity in females with X-linked Alport syndrome.
Suzuki R, Sakakibara N, Murakami S, Ichikawa Y, Kitakado H, Ueda C, Tanaka Y, Okada E, Kondo A, Aoto Y, Ishiko S, Ishimori S, Nagano C, Yamamura T, Horinouchi T, Okamoto T, Nozu K. Suzuki R, et al. Among authors: yamamura t. Nephrol Dial Transplant. 2024 Aug 12:gfae182. doi: 10.1093/ndt/gfae182. Online ahead of print. Nephrol Dial Transplant. 2024. PMID: 39134512
Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease.
Suzuki R, Sakakibara N, Ichikawa Y, Kitakado H, Ueda C, Tanaka Y, Okada E, Kondo A, Ishiko S, Ishimori S, Nagano C, Yamamura T, Horinouchi T, Okamoto T, Nozu K. Suzuki R, et al. Among authors: yamamura t. Kidney Int Rep. 2023 Jul 4;8(9):1811-1821. doi: 10.1016/j.ekir.2023.06.019. eCollection 2023 Sep. Kidney Int Rep. 2023. PMID: 37705905 Free PMC article.
Role of Iron in Children With Immunoglobulin A Nephropathy and Macrohematuria-Induced Acute Kidney Injury.
Ishimori S, Horinouchi T, Yamamura T, Fujimura J, Kamiyoshi N, Kaito H, Tanaka Y, Matsukura H, Shimabukuro W, Shima Y, Kawaguchi A, Araki Y, Nakanishi K, Hara S, Nozu K. Ishimori S, et al. Among authors: yamamura t. Kidney Int Rep. 2024 Mar 9;9(6):1664-1673. doi: 10.1016/j.ekir.2024.03.003. eCollection 2024 Jun. Kidney Int Rep. 2024. PMID: 38899207 Free PMC article.
Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population.
Jia X, Horinouchi T, Hitomi Y, Shono A, Khor SS, Omae Y, Kojima K, Kawai Y, Nagasaki M, Kaku Y, Okamoto T, Ohwada Y, Ohta K, Okuda Y, Fujimaru R, Hatae K, Kumagai N, Sawanobori E, Nakazato H, Ohtsuka Y, Nakanishi K, Shima Y, Tanaka R, Ashida A, Kamei K, Ishikura K, Nozu K, Tokunaga K, Iijima K; Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan. Jia X, et al. J Am Soc Nephrol. 2018 Aug;29(8):2189-2199. doi: 10.1681/ASN.2017080859. Epub 2018 Jul 16. J Am Soc Nephrol. 2018. PMID: 30012571 Free PMC article.
Corrigendum to "Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease"Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866.
Okada E, Morisada N, Horinouchi T, Fujii H, Tsuji T, Miura M, Katori H, Kitagawa M, Morozumi K, Toriyama T, Nakamura Y, Nishikomori R, Nagai S, Kondo A, Aoto Y, Ishiko S, Rossanti R, Sakakibara N, Nagano C, Yamamura T, Ishimori S, Usui J, Yamagata K, Iijima K, Imasawa T, Nozu K. Okada E, et al. Among authors: yamamura t. Kidney Int Rep. 2023 Mar 13;8(5):1127-1129. doi: 10.1016/j.ekir.2023.02.1090. eCollection 2023 May. Kidney Int Rep. 2023. PMID: 37180508 Free PMC article.
Trimerization profile of type IV collagen COL4A5 exon deletion in X-linked Alport syndrome.
Koyama Y, Suico MA, Owaki A, Sato R, Kuwazuru J, Kaseda S, Sannomiya Y, Horizono J, Omachi K, Horinouchi T, Yamamura T, Tsuhako H, Nozu K, Shuto T, Kai H. Koyama Y, et al. Among authors: yamamura t. Clin Exp Nephrol. 2024 Sep;28(9):874-881. doi: 10.1007/s10157-024-02503-9. Epub 2024 Apr 24. Clin Exp Nephrol. 2024. PMID: 38658441
1,304 results