Ichida F - Search Results

1

Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12.

Kenton AB, Sanchez X, Coveler KJ, Makar KA, Jimenez S, Ichida F, Murphy RT, Elliott PM, McKenna W, Bowles NE, Towbin JA, Bowles KR. Kenton AB, et al. Among authors: ichida f. Mol Genet Metab. 2004 Jun;82(2):162-6. doi: 10.1016/j.ymgme.2004.02.009. Mol Genet Metab. 2004. PMID: 15172004

2

Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome.

Ichida F, Tsubata S, Bowles KR, Haneda N, Uese K, Miyawaki T, Dreyer WJ, Messina J, Li H, Bowles NE, Towbin JA. Ichida F, et al. Circulation. 2001 Mar 6;103(9):1256-63. doi: 10.1161/01.cir.103.9.1256. Circulation. 2001. PMID: 11238270

3

Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction.

Chen R, Tsuji T, Ichida F, Bowles KR, Yu X, Watanabe S, Hirono K, Tsubata S, Hamamichi Y, Ohta J, Imai Y, Bowles NE, Miyawaki T, Towbin JA; Noncompaction study collaborators. Chen R, et al. Among authors: ichida f. Mol Genet Metab. 2002 Dec;77(4):319-25. doi: 10.1016/s1096-7192(02)00195-6. Mol Genet Metab. 2002. PMID: 12468278

4

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: ichida f. 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

5

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: ichida f. Mol Genet Metab. 2008 Apr;93(4):468-74. doi: 10.1016/j.ymgme.2007.10.009. Mol Genet Metab. 2008. PMID: 18368697

6

Left ventricular noncompaction.

Ichida F. Ichida F. Circ J. 2009 Jan;73(1):19-26. doi: 10.1253/circj.cj-08-0995. Epub 2008 Dec 4. Circ J. 2009. PMID: 19057090 Free article. Review.

7

Absence of parvoviral genomes in endothelial cells of Kawasaki disease patients with coronary artery lesions.

Bowles NE, Hirono K, Yu X, Ichida F. Bowles NE, et al. Among authors: ichida f. Pediatr Infect Dis J. 2009 Apr;28(4):345. doi: 10.1097/INF.0b013e318199302b. Pediatr Infect Dis J. 2009. PMID: 19238110 No abstract available.

8

Gonadal mosaicism of a TAZ (G4.5) mutation in a Japanese family with Barth syndrome and left ventricular noncompaction.

Chang B, Momoi N, Shan L, Mitomo M, Aoyagi Y, Endo K, Takeda I, Chen R, Xing Y, Yu X, Watanabe S, Yoshida T, Kanegane H, Tsubata S, Bowles NE, Ichida F, Miyawaki T; Noncompaction study collaborators. Chang B, et al. Among authors: ichida f. Mol Genet Metab. 2010 Jun;100(2):198-203. doi: 10.1016/j.ymgme.2010.02.021. Epub 2010 Mar 2. Mol Genet Metab. 2010. PMID: 20303308

9

Identification of a novel TPM1 mutation in a family with left ventricular noncompaction and sudden death.

Chang B, Nishizawa T, Furutani M, Fujiki A, Tani M, Kawaguchi M, Ibuki K, Hirono K, Taneichi H, Uese K, Onuma Y, Bowles NE, Ichida F, Inoue H, Matsuoka R, Miyawaki T; Noncompaction study collaborators. Chang B, et al. Among authors: ichida f. Mol Genet Metab. 2011 Feb;102(2):200-6. doi: 10.1016/j.ymgme.2010.09.009. Epub 2010 Sep 29. Mol Genet Metab. 2011. PMID: 20965760

10

14-3-3ε gene variants in a Japanese patient with left ventricular noncompaction and hypoplasia of the corpus callosum.

Chang B, Gorbea C, Lezin G, Li L, Shan L, Sakai N, Kogaki S, Otomo T, Okinaga T, Hamaoka A, Yu X, Hata Y, Nishida N, Yost HJ, Bowles NE, Brunelli L, Ichida F. Chang B, et al. Among authors: ichida f. Gene. 2013 Feb 15;515(1):173-80. doi: 10.1016/j.gene.2012.12.049. Epub 2012 Dec 20. Gene. 2013. PMID: 23266643

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