Iijima K - Search Results

1

Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.

Yamamura T, Nozu K, Minamikawa S, Horinouchi T, Sakakibara N, Nagano C, Aoto Y, Ishiko S, Nakanishi K, Shima Y, Nagase H, Rossanti R, Ye MJ, Nozu Y, Ishimori S, Morisada N, Kaito H, Iijima K. Yamamura T, et al. Among authors: iijima k. Mol Genet Genomic Med. 2019 Sep;7(9):e883. doi: 10.1002/mgg3.883. Epub 2019 Jul 30. Mol Genet Genomic Med. 2019. PMID: 31364286 Free PMC article. Clinical Trial.

2

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. 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.

3

Group A streptococcal antigen in the glomeruli of children with Henoch-Schönlein nephritis.

Masuda M, Nakanishi K, Yoshizawa N, Iijima K, Yoshikawa N. Masuda M, et al. Among authors: iijima k. Am J Kidney Dis. 2003 Feb;41(2):366-70. doi: 10.1053/ajkd.2003.50045. Am J Kidney Dis. 2003. PMID: 12552498

4

A-20C angiotensinogen gene polymorphism and proteinuria in childhood IgA nephropathy.

Nakanishi K, Sako M, Yata N, Aoyagi N, Nozu K, Tanaka R, Iijima K, Yoshikawa N. Nakanishi K, et al. Among authors: iijima k. Pediatr Nephrol. 2004 Feb;19(2):144-7. doi: 10.1007/s00467-003-1350-7. Epub 2003 Nov 28. Pediatr Nephrol. 2004. PMID: 14648325

5

Role of p38 MAP kinase pathway in a toxin-induced model of hemolytic uremic syndrome.

Fu XJ, Iijima K, Nozu K, Hamahira K, Tanaka R, Oda T, Yoshikawa N, Matsuo M. Fu XJ, et al. Among authors: iijima k. Pediatr Nephrol. 2004 Aug;19(8):844-52. doi: 10.1007/s00467-004-1502-4. Epub 2004 Jun 17. Pediatr Nephrol. 2004. PMID: 15206036

6

Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome.

Sako M, Nakanishi K, Obana M, Yata N, Hoshii S, Takahashi S, Wada N, Takahashi Y, Kaku Y, Satomura K, Ikeda M, Honda M, Iijima K, Yoshikawa N. Sako M, et al. Among authors: iijima k. Kidney Int. 2005 Apr;67(4):1248-55. doi: 10.1111/j.1523-1755.2005.00202.x. Kidney Int. 2005. PMID: 15780077 Free article.

7

Cyclosporin A absorption profiles in children with nephrotic syndrome.

Nozu K, Iijima K, Sakaeda T, Okumura K, Nakanishi K, Yoshikawa N, Honda M, Ikeda M, Matsuo M. Nozu K, et al. Among authors: iijima k. Pediatr Nephrol. 2005 Jul;20(7):910-3. doi: 10.1007/s00467-005-1844-6. Epub 2005 Apr 23. Pediatr Nephrol. 2005. PMID: 15856324

8

Rituximab treatment for posttransplant lymphoproliferative disorder (PTLD) induces complete remission of recurrent nephrotic syndrome.

Nozu K, Iijima K, Fujisawa M, Nakagawa A, Yoshikawa N, Matsuo M. Nozu K, et al. Among authors: iijima k. Pediatr Nephrol. 2005 Nov;20(11):1660-3. doi: 10.1007/s00467-005-2013-7. Epub 2005 Aug 16. Pediatr Nephrol. 2005. PMID: 16133051

9

Long-term follow-up of atypical membranoproliferative glomerulonephritis: are steroids indicated?

Fujita T, Nozu K, Iijima K, Kamioka I, Yoshiya K, Tanaka R, Hamahira K, Nakanishi K, Yoshikawa N, Matsuo M. Fujita T, et al. Among authors: iijima k. Pediatr Nephrol. 2006 Feb;21(2):194-200. doi: 10.1007/s00467-005-2074-7. Epub 2005 Oct 25. Pediatr Nephrol. 2006. PMID: 16247645

10

EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditions.

Okada M, Fujimaru R, Morimoto N, Satomura K, Kaku Y, Tsuzuki K, Nozu K, Okuyama T, Iijima K. Okada M, et al. Among authors: iijima k. Pediatr Nephrol. 2006 Apr;21(4):475-81. doi: 10.1007/s00467-006-0041-6. Epub 2006 Feb 21. Pediatr Nephrol. 2006. PMID: 16491411

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