Nakamura H - Search Results

1

PAX2 gene mutation in a family with isolated renal hypoplasia.

Nishimoto K, Iijima K, Shirakawa T, Kitagawa K, Satomura K, Nakamura H, Yoshikawa N. Nishimoto K, et al. Among authors: nakamura h. J Am Soc Nephrol. 2001 Aug;12(8):1769-1772. doi: 10.1681/ASN.V1281769. J Am Soc Nephrol. 2001. PMID: 11461952

2

Immunohistochemical analysis of renin activity in chronic cyclosporine nephropathy in childhood nephrotic syndrome.

Iijima K, Hamahira K, Kobayashi A, Nakamura H, Yoshikawa N. Iijima K, et al. Among authors: nakamura h. J Am Soc Nephrol. 2000 Dec;11(12):2265-2271. doi: 10.1681/ASN.V11122265. J Am Soc Nephrol. 2000. PMID: 11095649

3

Novel nonsense mutation in the Na+/HCO3- cotransporter gene (SLC4A4) in a patient with permanent isolated proximal renal tubular acidosis and bilateral glaucoma.

Igarashi T, Inatomi J, Sekine T, Seki G, Shimadzu M, Tozawa F, Takeshima Y, Takumi T, Takahashi T, Yoshikawa N, Nakamura H, Endou H. Igarashi T, et al. Among authors: nakamura h. J Am Soc Nephrol. 2001 Apr;12(4):713-718. doi: 10.1681/ASN.V124713. J Am Soc Nephrol. 2001. PMID: 11274232

4

Risk factors for cyclosporine-induced tubulointerstitial lesions in children with minimal change nephrotic syndrome.

Iijima K, Hamahira K, Tanaka R, Kobayashi A, Nozu K, Nakamura H, Yoshikawa N. Iijima K, et al. Among authors: nakamura h. Kidney Int. 2002 May;61(5):1801-5. doi: 10.1046/j.1523-1755.2002.00303.x. Kidney Int. 2002. PMID: 11967030 Free article. Clinical Trial.

5

Blockade of TGF-beta action ameliorates renal dysfunction and histologic progression in anti-GBM nephritis.

Zhou A, Ueno H, Shimomura M, Tanaka R, Shirakawa T, Nakamura H, Matsuo M, Iijima K. Zhou A, et al. Among authors: nakamura h. Kidney Int. 2003 Jul;64(1):92-101. doi: 10.1046/j.1523-1755.2003.00045.x. Kidney Int. 2003. PMID: 12787399 Free article.

6

Disorders of bilirubin binding to albumin and bilirubin-induced neurologic dysfunction.

Morioka I, Iwatani S, Koda T, Iijima K, Nakamura H. Morioka I, et al. Among authors: nakamura h. Semin Fetal Neonatal Med. 2015 Feb;20(1):31-36. doi: 10.1016/j.siny.2014.11.001. Epub 2014 Nov 26. Semin Fetal Neonatal Med. 2015. PMID: 25432488 Review.

7

Association of HMOX1 gene promoter polymorphisms with hyperbilirubinemia in the early neonatal period.

Katayama Y, Yokota T, Zhao H, Wong RJ, Stevenson DK, Taniguchi-Ikeda M, Nakamura H, Iijima K, Morioka I. Katayama Y, et al. Among authors: nakamura h. Pediatr Int. 2015 Aug;57(4):645-9. doi: 10.1111/ped.12591. Epub 2015 Apr 28. Pediatr Int. 2015. PMID: 25625535

8

Evaluation of BiliCare™ transcutaneous bilirubin device in Japanese newborns.

Yamana K, Morioka I, Kurokawa D, Fukushima S, Nishida K, Ohyama S, Nishimura N, Nozu K, Taniguchi-Ikeda M, Nagase H, Fujioka K, Iwatani S, Nakamura H, Iijima K. Yamana K, et al. Among authors: nakamura h. Pediatr Int. 2017 Oct;59(10):1058-1063. doi: 10.1111/ped.13364. Epub 2017 Aug 31. Pediatr Int. 2017. PMID: 28703875 Clinical Trial.

9

Novel treatment strategy for Japanese newborns with high serum unbound bilirubin.

Yokota T, Morioka I, Kodera T, Morisawa T, Sato I, Kawano S, Koda T, Matsuo K, Fujioka K, Morikawa S, Miwa A, Shibata A, Yokoyama N, Yonetani M, Yamada H, Nakamura H, Iijima K. Yokota T, et al. Among authors: nakamura h. Pediatr Int. 2013 Feb;55(1):54-9. doi: 10.1111/j.1442-200X.2012.03726.x. Epub 2012 Dec 11. Pediatr Int. 2013. PMID: 22978498 Clinical Trial.

10

Fluorescent protein-based detection of unconjugated bilirubin in newborn serum.

Iwatani S, Nakamura H, Kurokawa D, Yamana K, Nishida K, Fukushima S, Koda T, Nishimura N, Nishio H, Iijima K, Miyawaki A, Morioka I. Iwatani S, et al. Among authors: nakamura h. Sci Rep. 2016 Jun 21;6:28489. doi: 10.1038/srep28489. Sci Rep. 2016. PMID: 27324682 Free PMC article.

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