Ishimori S - Search Results

1

Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases.

Ishiko S, Horinouchi T, Fujimaru R, Shima Y, Kaito H, Tanaka R, Ishimori S, Kondo A, Nagai S, Aoto Y, Sakakibara N, Nagano C, Yamamura T, Yoshimura M, Nakanishi K, Fujimura J, Kamiyoshi N, Nagase H, Yoshikawa N, Iijima K, Nozu K. Ishiko S, et al. Among authors: ishimori s. Sci Rep. 2020 Aug 20;10(1):14026. doi: 10.1038/s41598-020-71101-y. Sci Rep. 2020. PMID: 32820208 Free PMC article.

2

Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method.

Hashimoto F, Nishiumi S, Miyake O, Takeichi H, Chitose M, Ohtsubo H, Ishimori S, Ninchoji T, Hashimura Y, Kaito H, Morisada N, Morioka I, Fukuoka H, Yoshida M, Iijima K. Hashimoto F, et al. Among authors: ishimori s. Early Hum Dev. 2013 May;89(5):315-20. doi: 10.1016/j.earlhumdev.2012.10.010. Epub 2012 Nov 22. Early Hum Dev. 2013. PMID: 23178109

3

Acute kidney injury after acute gastroenteritis in an infant with hereditary hypouricemia.

Kamei K, Ogura M, Ishimori S, Kaito H, Iijima K, Ito S. Kamei K, et al. Among authors: ishimori s. Eur J Pediatr. 2014 Feb;173(2):247-9. doi: 10.1007/s00431-013-2010-y. Epub 2013 May 8. Eur J Pediatr. 2014. PMID: 23652934

4

SLC26A3 gene analysis in patients with Bartter and Gitelman syndromes and the clinical characteristics of patients with unidentified mutations.

Ishimori S, Kaito H, Matsunoshita N, Otsubo H, Hashimoto F, Ninchoji T, Nozu K, Morisada N, Iijima K. Ishimori S, et al. Kobe J Med Sci. 2013 Apr 18;59(2):E36-43. Kobe J Med Sci. 2013. PMID: 23756661 Free article.

5

Molecular background of urate transporter genes in patients with exercise-induced acute kidney injury.

Kaito H, Ishimori S, Nozu K, Shima Y, Nakanishi K, Yoshikawa N, Iijima K. Kaito H, et al. Among authors: ishimori s. Am J Nephrol. 2013;38(4):316-20. doi: 10.1159/000355430. Epub 2013 Oct 4. Am J Nephrol. 2013. PMID: 24107611

6

Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain.

Hashimura Y, Nozu K, Kaito H, Nakanishi K, Fu XJ, Ohtsubo H, Hashimoto F, Oka M, Ninchoji T, Ishimori S, Morisada N, Matsunoshita N, Kamiyoshi N, Yoshikawa N, Iijima K. Hashimura Y, et al. Among authors: ishimori s. Kidney Int. 2014 May;85(5):1208-13. doi: 10.1038/ki.2013.479. Epub 2013 Dec 4. Kidney Int. 2014. PMID: 24304881 Free article.

7

16q12 microdeletion syndrome in two Japanese boys.

Morisada N, Sekine T, Ishimori S, Tsuda M, Adachi M, Nozu K, Nakanishi K, Tanaka R, Iijima K. Morisada N, et al. Among authors: ishimori s. Pediatr Int. 2014 Oct;56(5):e75-8. doi: 10.1111/ped.12426. Pediatr Int. 2014. PMID: 25336016

8

Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencing.

Yamamura T, Morisada N, Nozu K, Minamikawa S, Ishimori S, Toyoshima D, Ninchoji T, Yasui M, Taniguchi-Ikeda M, Morioka I, Nakanishi K, Nishio H, Iijima K. Yamamura T, et al. Among authors: ishimori s. Clin Exp Nephrol. 2017 Feb;21(1):136-142. doi: 10.1007/s10157-016-1256-x. Epub 2016 Mar 11. Clin Exp Nephrol. 2017. PMID: 26968886

9

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: ishimori s. 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

10

Clinical characteristics and long-term outcome of diarrhea-associated hemolytic uremic syndrome: a single center experience.

Ninchoji T, Nozu K, Nakanishi K, Horinouchi T, Fujimura J, Yamamura T, Minamikawa S, Ishimori S, Nakanishi K, Yoshikawa N, Morioka I, Kaito H, Iijima K. Ninchoji T, et al. Among authors: ishimori s. Clin Exp Nephrol. 2017 Oct;21(5):889-894. doi: 10.1007/s10157-016-1376-3. Epub 2017 Jan 10. Clin Exp Nephrol. 2017. PMID: 28074307

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