Futatani T - Search Results

1

Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.

Futatani T, Nii E, Obata M, Ichida F, Okabe Y, Kanegane H, Miyawaki T. Futatani T, et al. Pediatr Int. 2008 Feb;50(1):116-8. doi: 10.1111/j.1442-200X.2007.02505.x. Pediatr Int. 2008. PMID: 18279219 No abstract available.

2

[Primary immunodeficiency diseases].

Futatani T, Kanegane H, Miyawaki T. Futatani T, et al. Nihon Rinsho. 2005 May;63 Suppl 5:559-64. Nihon Rinsho. 2005. PMID: 15954409 Review. Japanese. No abstract available.

3

Severe neutropenia in Japanese patients with x-linked agammaglobulinemia.

Kanegane H, Taneichi H, Nomura K, Futatani T, Miyawaki T. Kanegane H, et al. Among authors: futatani t. J Clin Immunol. 2005 Sep;25(5):491-5. doi: 10.1007/s10875-005-5370-x. J Clin Immunol. 2005. PMID: 16160918

4

SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmia.

Shan L, Makita N, Xing Y, Watanabe S, Futatani T, Ye F, Saito K, Ibuki K, Watanabe K, Hirono K, Uese K, Ichida F, Miyawaki T, Origasa H, Bowles NE, Towbin JA. Shan L, et al. Among authors: futatani t. Mol Genet Metab. 2008 Apr;93(4):468-74. doi: 10.1016/j.ymgme.2007.10.009. Mol Genet Metab. 2008. PMID: 18368697

5

Neutrophils and mononuclear cells express vascular endothelial growth factor in acute Kawasaki disease: its possible role in progression of coronary artery lesions.

Hamamichi Y, Ichida F, Yu X, Hirono KI, Uese KI, Hashimoto I, Tsubata S, Yoshida T, Futatani T, Kanegane H, Miyawaki T. Hamamichi Y, et al. Among authors: futatani t. Pediatr Res. 2001 Jan;49(1):74-80. doi: 10.1203/00006450-200101000-00017. Pediatr Res. 2001. PMID: 11134495

6

Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia.

Shinomiya N, Kanegane H, Watanabe A, Yamaguchi Y, Futatani T, Miyawaki T. Shinomiya N, et al. Among authors: futatani t. Pediatr Int. 2000 Dec;42(6):689-92. doi: 10.1046/j.1442-200x.2000.01293.x. Pediatr Int. 2000. PMID: 11192530 No abstract available.

7

Novel mutations in a Japanese patient with CD19 deficiency.

Kanegane H, Agematsu K, Futatani T, Sira MM, Suga K, Sekiguchi T, van Zelm MC, Miyawaki T. Kanegane H, et al. Among authors: futatani t. Genes Immun. 2007 Dec;8(8):663-70. doi: 10.1038/sj.gene.6364431. Epub 2007 Sep 20. Genes Immun. 2007. PMID: 17882224

8

Novel Igalpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia.

Wang Y, Kanegane H, Sanal O, Tezcan I, Ersoy F, Futatani T, Miyawaki T. Wang Y, et al. Among authors: futatani t. Am J Med Genet. 2002 Apr 1;108(4):333-6. doi: 10.1002/ajmg.10296. Am J Med Genet. 2002. PMID: 11920841

9

Autoimmune lymphoproliferative syndrome presenting with glomerulonephritis.

Kanegane H, Vilela MM, Wang Y, Futatani T, Matsukura H, Miyawaki T. Kanegane H, et al. Among authors: futatani t. Pediatr Nephrol. 2003 May;18(5):454-6. doi: 10.1007/s00467-003-1087-3. Epub 2003 Apr 4. Pediatr Nephrol. 2003. PMID: 12736807

10

Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity.

Xing Y, Ichida F, Matsuoka T, Isobe T, Ikemoto Y, Higaki T, Tsuji T, Haneda N, Kuwabara A, Chen R, Futatani T, Tsubata S, Watanabe S, Watanabe K, Hirono K, Uese K, Miyawaki T, Bowles KR, Bowles NE, Towbin JA. Xing Y, et al. Among authors: futatani t. Mol Genet Metab. 2006 May;88(1):71-7. doi: 10.1016/j.ymgme.2005.11.009. Epub 2006 Jan 19. Mol Genet Metab. 2006. PMID: 16427346

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