Nozu K - Search Results

1

Familial focal segmental glomerulosclerosis with PLCE1 mutation in siblings.

Shimizu M, Irabu H, Kaneda H, Ohta K, Nozu K. Shimizu M, et al. Among authors: nozu k. Pediatr Int. 2019 Jul;61(7):726-727. doi: 10.1111/ped.13870. Pediatr Int. 2019. PMID: 31359539 No abstract available.

2

Risk factors for developing severe clinical course in HUS patients: a national survey in Japan.

Kamioka I, Yoshiya K, Satomura K, Kaito H, Fujita T, Iijima K, Nakanishi K, Yoshikawa N, Nozu K, Matsuo M; Japanese Society for Pediatric Nephrology. Kamioka I, et al. Among authors: nozu k. Pediatr Int. 2008 Aug;50(4):441-6. doi: 10.1111/j.1442-200X.2008.02605.x. Pediatr Int. 2008. PMID: 19143964

3

A surviving case of papillorenal syndrome with the phenotype of Potter sequence.

Fujioka K, Morioka I, Nozu K, Nishimoto M, Amano M, Tagami M, Honda S, Yokoyama N, Yamada H, Iijima K, Matsuo M. Fujioka K, et al. Among authors: nozu k. Pediatr Int. 2011 Jun;53(3):406-8. doi: 10.1111/j.1442-200X.2010.03261.x. Pediatr Int. 2011. PMID: 21696512 No abstract available.

4

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: nozu k. Pediatrics. 2012 Jun;129(6):e1621-5. doi: 10.1542/peds.2011-1323. Epub 2012 May 14. Pediatrics. 2012. PMID: 22585769

5

Branchio-oto-renal syndrome: comprehensive review based on nationwide surveillance in Japan.

Morisada N, Nozu K, Iijima K. Morisada N, et al. Among authors: nozu k. Pediatr Int. 2014 Jun;56(3):309-14. doi: 10.1111/ped.12357. Pediatr Int. 2014. PMID: 24730701 Review.

6

A multicenter randomized trial indicates initial prednisolone treatment for childhood nephrotic syndrome for two months is not inferior to six-month treatment.

Yoshikawa N, Nakanishi K, Sako M, Oba MS, Mori R, Ota E, Ishikura K, Hataya H, Honda M, Ito S, Shima Y, Kaito H, Nozu K, Nakamura H, Igarashi T, Ohashi Y, Iijima K; Japanese Study Group of Kidney Disease in Children. Yoshikawa N, et al. Among authors: nozu k. Kidney Int. 2015 Jan;87(1):225-32. doi: 10.1038/ki.2014.260. Epub 2014 Jul 23. Kidney Int. 2015. PMID: 25054775 Free PMC article. Clinical Trial.

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: nozu k. Pediatr Int. 2014 Oct;56(5):e75-8. doi: 10.1111/ped.12426. Pediatr Int. 2014. PMID: 25336016

8

Combined Alport syndrome and Klinefelter syndrome.

Nishida M, Hashimoto F, Kaito H, Nozu K, Iijima K, Asada D, Hamaoka K. Nishida M, et al. Among authors: nozu k. Pediatr Int. 2016 Feb;58(2):152-5. doi: 10.1111/ped.12743. Epub 2015 Nov 10. Pediatr Int. 2016. PMID: 26554353

9

Transient hyperphosphatasemia in three pediatric patients treated with cyclosporine.

Mori T, Tanaka R, Nishida K, Yamamoto N, Hayakawa A, Nishimura N, Nozu K, Iijima K. Mori T, et al. Among authors: nozu k. Pediatr Int. 2016 May;58(5):429-30. doi: 10.1111/ped.12923. Pediatr Int. 2016. PMID: 27173422

10

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: nozu k, nozu y. 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

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