Ikeda M - Search Results

1

Genetic and enzymatic analysis for two Japanese patients with idiopathic infantile arterial calcification.

Numakura C, Yamada M, Ariyasu D, Maesaka A, Kobayashi H, Nishimura G, Ikeda M, Hasegawa Y. Numakura C, et al. Among authors: ikeda m. J Bone Miner Metab. 2006;24(1):48-52. doi: 10.1007/s00774-005-0645-0. J Bone Miner Metab. 2006. PMID: 16369898

2

WT1 intron 9 splice acceptor site mutation in a 46,XY male with focal segmental glomerulosclerosis.

Kanemoto K, Ishikura K, Ariyasu D, Hamasaki Y, Hataya H, Hasegawa Y, Ikeda M. Kanemoto K, et al. Among authors: ikeda m. Pediatr Nephrol. 2007 Mar;22(3):454-8. doi: 10.1007/s00467-006-0333-x. Epub 2006 Oct 24. Pediatr Nephrol. 2007. PMID: 17061122

3

Gonadal Function in 15 Patients Associated with WT1 Gene Mutations.

Maesaka A, Higuchi A, Kotoh S, Hasegawa Y, Ikeda M, Shishido S, Honda M. Maesaka A, et al. Among authors: ikeda m. Clin Pediatr Endocrinol. 2006;15(4):143-9. doi: 10.1297/cpe.15.143. Epub 2006 Nov 3. Clin Pediatr Endocrinol. 2006. PMID: 24790335 Free PMC article.

4

Nephrotic state as a risk factor for developing posterior reversible encephalopathy syndrome in paediatric patients with nephrotic syndrome.

Ishikura K, Ikeda M, Hamasaki Y, Hataya H, Nishimura G, Hiramoto R, Honda M. Ishikura K, et al. Among authors: ikeda m. Nephrol Dial Transplant. 2008 Aug;23(8):2531-6. doi: 10.1093/ndt/gfn013. Epub 2008 Feb 7. Nephrol Dial Transplant. 2008. PMID: 18258739

5

Posterior reversible encephalopathy syndrome in children: its high prevalence and more extensive imaging findings.

Ishikura K, Ikeda M, Hamasaki Y, Hataya H, Shishido S, Asanuma H, Nishimura G, Hiramoto R, Honda M. Ishikura K, et al. Among authors: ikeda m. Am J Kidney Dis. 2006 Aug;48(2):231-8. doi: 10.1053/j.ajkd.2006.04.076. Am J Kidney Dis. 2006. PMID: 16860188

6

Bifid epiglottis: syndromic constituent rather than isolated anomaly.

Tsurumi H, Ito M, Ishikura K, Hataya H, Ikeda M, Honda M, Nishimura G. Tsurumi H, et al. Among authors: ikeda m. Pediatr Int. 2010 Oct;52(5):723-8. doi: 10.1111/j.1442-200X.2010.03096.x. Pediatr Int. 2010. PMID: 20149127

7

The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia.

Komoda F, Sekine T, Inatomi J, Enomoto A, Endou H, Ota T, Matsuyama T, Ogata T, Ikeda M, Awazu M, Muroya K, Kamimaki I, Igarashi T. Komoda F, et al. Among authors: ikeda m. Pediatr Nephrol. 2004 Jul;19(7):728-33. doi: 10.1007/s00467-004-1424-1. Epub 2004 Mar 31. Pediatr Nephrol. 2004. PMID: 15054642

8

An infantile case of Hinman syndrome with severe acute renal failure.

Chaichanamongkol V, Ikeda M, Ishikura K, Hamasaki Y, Hataya H, Satoh H, Asanuma H, Shishido S, Honda M. Chaichanamongkol V, et al. Among authors: ikeda m. Clin Exp Nephrol. 2008 Aug;12(4):309-311. doi: 10.1007/s10157-008-0048-3. Epub 2008 Apr 15. Clin Exp Nephrol. 2008. PMID: 18409063

9

Typical MPGN with few urinary abnormalities.

Yata N, Ikeda M, Ishikura K, Hataya H, Matsuyama T, Banba M, Hasegawa O, Honda M. Yata N, et al. Among authors: ikeda m. Am J Kidney Dis. 2004 May;43(5):918-22. doi: 10.1053/j.ajkd.2003.12.053. Am J Kidney Dis. 2004. PMID: 15112183

10

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: ikeda m. Kidney Int. 2005 Apr;67(4):1248-55. doi: 10.1111/j.1523-1755.2005.00202.x. Kidney Int. 2005. PMID: 15780077 Free article.

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