Nakanishi K - Search Results

1

Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group.

Kashtan CE, Ding J, Garosi G, Heidet L, Massella L, Nakanishi K, Nozu K, Renieri A, Rheault M, Wang F, Gross O. Kashtan CE, et al. Among authors: nakanishi k. Kidney Int. 2018 May;93(5):1045-1051. doi: 10.1016/j.kint.2017.12.018. Epub 2018 Mar 16. Kidney Int. 2018. PMID: 29551517 Free article.

2

Epithelial-to-mesenchymal transition in cyst lining epithelial cells in an orthologous PCK rat model of autosomal-recessive polycystic kidney disease.

Togawa H, Nakanishi K, Mukaiyama H, Hama T, Shima Y, Sako M, Miyajima M, Nozu K, Nishii K, Nagao S, Takahashi H, Iijima K, Yoshikawa N. Togawa H, et al. Among authors: nakanishi k. Am J Physiol Renal Physiol. 2011 Feb;300(2):F511-20. doi: 10.1152/ajprenal.00038.2010. Epub 2010 Nov 17. Am J Physiol Renal Physiol. 2011. PMID: 21084407 Free article.

3

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: nakanishi k. Pediatr Nephrol. 2011 Apr;26(4):563-9. doi: 10.1007/s00467-010-1741-5. Epub 2011 Jan 4. Pediatr Nephrol. 2011. PMID: 21203777

4

Recurrent EIARF and PRES with severe renal hypouricemia by compound heterozygous SLC2A9 mutation.

Shima Y, Nozu K, Nozu Y, Togawa H, Kaito H, Matsuo M, Iijima K, Nakanishi K, Yoshikawa N. Shima Y, et al. Among authors: nakanishi k. Pediatrics. 2011 Jun;127(6):e1621-5. doi: 10.1542/peds.2010-2592. Epub 2011 May 2. Pediatrics. 2011. PMID: 21536615

5

Alport-like glomerular basement membrane changes with renal-coloboma syndrome.

Ohtsubo H, Morisada N, Kaito H, Nagatani K, Nakanishi K, Iijima K. Ohtsubo H, et al. Among authors: nakanishi k. Pediatr Nephrol. 2012 Jul;27(7):1189-92. doi: 10.1007/s00467-012-2125-9. Epub 2012 Feb 21. Pediatr Nephrol. 2012. PMID: 22350371

6

Focal segmental glomerulosclerosis in patients with complete deletion of one WT1 allele.

Iijima K, Someya T, Ito S, Nozu K, Nakanishi K, Matsuoka K, Ohashi H, Nagata M, Kamei K, Sasaki S. Iijima K, et al. Among authors: nakanishi k. Pediatrics. 2012 Jun;129(6):e1621-5. doi: 10.1542/peds.2011-1323. Epub 2012 May 14. Pediatrics. 2012. PMID: 22585769

7

Endoplasmic reticulum stress with low-dose cyclosporine in frequently relapsing nephrotic syndrome.

Hama T, Nakanishi K, Mukaiyama H, Shima Y, Togawa H, Sako M, Nozu K, Iijima K, Yoshikawa N. Hama T, et al. Among authors: nakanishi k. Pediatr Nephrol. 2013 Jun;28(6):903-9. doi: 10.1007/s00467-012-2403-6. Epub 2013 Jan 15. Pediatr Nephrol. 2013. PMID: 23318599

8

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: nakanishi k. Am J Nephrol. 2013;38(4):316-20. doi: 10.1159/000355430. Epub 2013 Oct 4. Am J Nephrol. 2013. PMID: 24107611

9

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: nakanishi k. 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.

10

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: nakanishi k. Pediatr Nephrol. 2014 Sep;29(9):1535-44. doi: 10.1007/s00467-014-2797-4. Epub 2014 Mar 15. Pediatr Nephrol. 2014. PMID: 24633401

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