Yoshikawa N - Search Results

1

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: yoshikawa n. Am J Kidney Dis. 2003 Feb;41(2):366-70. doi: 10.1053/ajkd.2003.50045. Am J Kidney Dis. 2003. PMID: 12552498

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

3

PAX2 gene mutation in a family with isolated renal hypoplasia.

Nishimoto K, Iijima K, Shirakawa T, Kitagawa K, Satomura K, Nakamura H, Yoshikawa N. Nishimoto K, et al. Among authors: yoshikawa n. J Am Soc Nephrol. 2001 Aug;12(8):1769-1772. doi: 10.1681/ASN.V1281769. J Am Soc Nephrol. 2001. PMID: 11461952

4

Long-term outcome of focal segmental glomerulosclerosis after Japanese pediatric renal transplantation.

Fujisawa M, Iijima K, Ishimura T, Higuchi A, Isotani S, Yoshiya K, Arakawa S, Hamami G, Matsumoto O, Yoshikawa N, Kamidono S. Fujisawa M, et al. Among authors: yoshikawa n. Pediatr Nephrol. 2002 Mar;17(3):165-8. doi: 10.1007/s00467-001-0759-0. Pediatr Nephrol. 2002. PMID: 11956852

5

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. Among authors: yoshikawa n. 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.

6

Quality of life of living kidney donors: the short-form 36-item health questionnaire survey.

Isotani S, Fujisawa M, Ichikawa Y, Ishimura T, Matsumoto O, Hamami G, Arakawa S, Iijima K, Yoshikawa N, Nagano S, Kamidono S. Isotani S, et al. Among authors: yoshikawa n. Urology. 2002 Oct;60(4):588-92; discussion 592. doi: 10.1016/s0090-4295(02)01865-4. Urology. 2002. PMID: 12385912

7

Endothelial nitric oxide synthase expression in ischemia-reperfusion injury after living related-donor renal transplantation.

Ishimura T, Fujisawa M, Isotani S, Iijima K, Yoshikawa N, Kamidono S. Ishimura T, et al. Among authors: yoshikawa n. Transpl Int. 2002 Dec;15(12):635-40. doi: 10.1007/s00147-002-0473-2. Epub 2002 Oct 19. Transpl Int. 2002. PMID: 12478411

8

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: yoshikawa n. Pediatr Nephrol. 2003 May;18(5):412-6. doi: 10.1007/s00467-003-1120-6. Epub 2003 Apr 5. Pediatr Nephrol. 2003. PMID: 12687458

9

Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT).

Nakanishi K, Yoshikawa N. Nakanishi K, et al. Among authors: yoshikawa n. Pediatr Int. 2003 Oct;45(5):610-6. doi: 10.1046/j.1442-200x.2003.01779.x. Pediatr Int. 2003. PMID: 14521546 Review.

10

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: yoshikawa n. Pediatr Nephrol. 2004 Feb;19(2):144-7. doi: 10.1007/s00467-003-1350-7. Epub 2003 Nov 28. Pediatr Nephrol. 2004. PMID: 14648325

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