Iijima K - Search Results

1

Biallelic variants/mutations of IL1RAP in patients with steroid-sensitive nephrotic syndrome.

Niitsuma S, Kudo H, Kikuchi A, Hayashi T, Kumakura S, Kobayashi S, Okuyama Y, Kumagai N, Niihori T, Aoki Y, So T, Funayama R, Nakayama K, Shirota M, Kondo S, Kagami S, Tsukaguchi H, Iijima K, Kure S, Ishii N. Niitsuma S, et al. Among authors: iijima k. Int Immunol. 2020 Apr 12;32(4):283-292. doi: 10.1093/intimm/dxz081. Int Immunol. 2020. PMID: 31954058

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. J Am Soc Nephrol. 2000 Dec;11(12):2265-2271. doi: 10.1681/ASN.V11122265. J Am Soc Nephrol. 2000. PMID: 11095649

3

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.

4

NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.

Maruyama K, Iijima K, Ikeda M, Kitamura A, Tsukaguchi H, Yoshiya K, Hoshii S, Wada N, Uemura O, Satomura K, Honda M, Yoshikawa N. Maruyama K, et al. Among authors: iijima k. Pediatr Nephrol. 2003 May;18(5):412-6. doi: 10.1007/s00467-003-1120-6. Epub 2003 Apr 5. Pediatr Nephrol. 2003. PMID: 12687458

5

Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome.

Kitamura A, Tsukaguchi H, Iijima K, Araki J, Hattori M, Ikeda M, Honda M, Nozu K, Nakazato H, Yoshikawa N, Kagami S, Muramatsu M, Choi Y, Cheong HI, Doi T. Kitamura A, et al. Among authors: iijima k. Nephrol Dial Transplant. 2006 Nov;21(11):3133-8. doi: 10.1093/ndt/gfl347. Epub 2006 Sep 12. Nephrol Dial Transplant. 2006. PMID: 16968734 No abstract available.

6

Steroid-resistant nephrotic syndrome.

Kitamura A, Tsukaguchi H, Maruyama K, Shono A, Iijima K, Kagami S, Doi T. Kitamura A, et al. Among authors: iijima k. Kidney Int. 2008 Nov;74(9):1209-15. doi: 10.1038/ki.2008.297. Epub 2008 Jul 2. Kidney Int. 2008. PMID: 18596732 Free article. No abstract available.

7

Predisposition to relapsing nephrotic syndrome by a nephrin mutation that interferes with assembly of functioning microdomains.

Shono A, Tsukaguchi H, Kitamura A, Hiramoto R, Qin XS, Doi T, Iijima K. Shono A, et al. Among authors: iijima k. Hum Mol Genet. 2009 Aug 15;18(16):2943-56. doi: 10.1093/hmg/ddp232. Epub 2009 May 14. Hum Mol Genet. 2009. PMID: 19443487

8

[Molecular basis of hereditary nephrotic syndromes].

Iijima K, Tsukaguchi H. Iijima K, et al. Nihon Jinzo Gakkai Shi. 2010;52(7):914-23. Nihon Jinzo Gakkai Shi. 2010. PMID: 21077341 Review. Japanese. No abstract available.

9

Rituximab for childhood refractory nephrotic syndrome.

Iijima K. Iijima K. Pediatr Int. 2011 Oct;53(5):617-621. doi: 10.1111/j.1442-200X.2011.03432.x. Pediatr Int. 2011. PMID: 21771179 Review.

10

Identification of FOXP3-negative regulatory T-like (CD4(+)CD25(+)CD127(low)) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.

Otsubo K, Kanegane H, Kamachi Y, Kobayashi I, Tsuge I, Imaizumi M, Sasahara Y, Hayakawa A, Nozu K, Iijima K, Ito S, Horikawa R, Nagai Y, Takatsu K, Mori H, Ochs HD, Miyawaki T. Otsubo K, et al. Among authors: iijima k. Clin Immunol. 2011 Oct;141(1):111-20. doi: 10.1016/j.clim.2011.06.006. Epub 2011 Jul 12. Clin Immunol. 2011. PMID: 21802372

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