Hashimura Y - Search Results

1

Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity.

Ninchoji T, Kaito H, Nozu K, Hashimura Y, Kanda K, Kamioka I, Shima Y, Hamahira K, Nakanishi K, Tanaka R, Yoshikawa N, Iijima K, Matsuo M. Ninchoji T, et al. Among authors: hashimura y. Pediatr Nephrol. 2011 Apr;26(4):563-9. doi: 10.1007/s00467-010-1741-5. Epub 2011 Jan 4. Pediatr Nephrol. 2011. PMID: 21203777

2

Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.

Nozu K, Przybyslaw Krol R, Ohtsuka Y, Nakanishi K, Yoshikawa N, Nozu Y, Kaito H, Kanda K, Hashimura Y, Hamasaki Y, Iijima K, Matsuo M. Nozu K, et al. Among authors: hashimura y. Pediatr Nephrol. 2008 Nov;23(11):2085-90. doi: 10.1007/s00467-008-0878-y. Epub 2008 Jun 27. Pediatr Nephrol. 2008. PMID: 18584212

3

Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.

Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iijima K, Matsuo M. Hashimura Y, et al. Pediatr Nephrol. 2009 Jun;24(6):1181-6. doi: 10.1007/s00467-009-1119-8. Epub 2009 Feb 3. Pediatr Nephrol. 2009. PMID: 19189134

4

The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids.

Kanda K, Nozu K, Kaito H, Iijima K, Nakanishi K, Yoshikawa N, Ninchoji T, Hashimura Y, Matsuo M, Moritz ML. Kanda K, et al. Among authors: hashimura y. Pediatr Nephrol. 2011 Jan;26(1):99-104. doi: 10.1007/s00467-010-1647-2. Epub 2010 Oct 16. Pediatr Nephrol. 2011. PMID: 20953635

5

Validity of the Oxford classification of IgA nephropathy in children.

Shima Y, Nakanishi K, Hama T, Mukaiyama H, Togawa H, Hashimura Y, Kaito H, Sako M, Iijima K, Yoshikawa N. Shima Y, et al. Among authors: hashimura y. Pediatr Nephrol. 2012 May;27(5):783-92. doi: 10.1007/s00467-011-2061-0. Epub 2011 Dec 2. Pediatr Nephrol. 2012. PMID: 22134880

6

Natural history of genetically proven autosomal recessive Alport syndrome.

Oka M, Nozu K, Kaito H, Fu XJ, Nakanishi K, Hashimura Y, Morisada N, Yan K, Matsuo M, Yoshikawa N, Vorechovsky I, Iijima K. Oka M, et al. Among authors: hashimura y. Pediatr Nephrol. 2014 Sep;29(9):1535-44. doi: 10.1007/s00467-014-2797-4. Epub 2014 Mar 15. Pediatr Nephrol. 2014. PMID: 24633401

7

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene.

Kanda K, Nozu K, Yokoyama N, Morioka I, Miwa A, Hashimura Y, Kaito H, Iijima K, Matsuo M. Kanda K, et al. Among authors: hashimura y. BMC Nephrol. 2009 Nov 14;10:37. doi: 10.1186/1471-2369-10-37. BMC Nephrol. 2009. PMID: 19912655 Free PMC article.

8

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. 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.

9

Two cases of atypical membranoproliferative glomerulonephritis showing opposite clinical course.

Hashimura Y, Kaito H, Nozu K, Shima Y, Nakanishi K, Iijima K, Yoshikawa N. Hashimura Y, et al. CEN Case Rep. 2012 May;1(1):34-38. doi: 10.1007/s13730-012-0009-2. Epub 2012 Apr 10. CEN Case Rep. 2012. PMID: 28509151 Free PMC article.

10

In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation.

Nozu K, Iijima K, Kawai K, Nozu Y, Nishida A, Takeshima Y, Fu XJ, Hashimura Y, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M. Nozu K, et al. Among authors: hashimura y. Hum Genet. 2009 Oct;126(4):533-8. doi: 10.1007/s00439-009-0697-7. Epub 2009 Jun 10. Hum Genet. 2009. PMID: 19513753

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