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340 results

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Page 1
Role of TBX1 in human del22q11.2 syndrome.
Yagi H, Furutani Y, Hamada H, Sasaki T, Asakawa S, Minoshima S, Ichida F, Joo K, Kimura M, Imamura S, Kamatani N, Momma K, Takao A, Nakazawa M, Shimizu N, Matsuoka R. Yagi H, et al. Among authors: ichida f. Lancet. 2003 Oct 25;362(9393):1366-73. doi: 10.1016/s0140-6736(03)14632-6. Lancet. 2003. PMID: 14585638
Outcomes of childhood pulmonary arterial hypertension in BMPR2 and ALK1 mutation carriers.
Chida A, Shintani M, Yagi H, Fujiwara M, Kojima Y, Sato H, Imamura S, Yokozawa M, Onodera N, Horigome H, Kobayashi T, Hatai Y, Nakayama T, Fukushima H, Nishiyama M, Doi S, Ono Y, Yasukouchi S, Ichida F, Fujimoto K, Ohtsuki S, Teshima H, Kawano T, Nomura Y, Gu H, Ishiwata T, Furutani Y, Inai K, Saji T, Matsuoka R, Nonoyama S, Nakanishi T. Chida A, et al. Among authors: ichida f. Am J Cardiol. 2012 Aug 15;110(4):586-93. doi: 10.1016/j.amjcard.2012.04.035. Epub 2012 May 25. Am J Cardiol. 2012. PMID: 22632830
Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy.
Chida A, Inai K, Sato H, Shimada E, Nishizawa T, Shimada M, Furutani M, Furutani Y, Kawamura Y, Sugimoto M, Ishihara J, Fujiwara M, Soga T, Kawana M, Fuji S, Tateno S, Kuraishi K, Kogaki S, Nishimura M, Ayusawa M, Ichida F, Yamazawa H, Matsuoka R, Nonoyama S, Nakanishi T. Chida A, et al. Among authors: ichida f. Heart Vessels. 2017 Jun;32(6):700-707. doi: 10.1007/s00380-016-0920-0. Epub 2016 Nov 24. Heart Vessels. 2017. PMID: 27885498
Expression of myeloid-related protein-8 and -14 in patients with acute Kawasaki disease.
Hirono K, Foell D, Xing Y, Miyagawa-Tomita S, Ye F, Ahlmann M, Vogl T, Futatani T, Rui C, Yu X, Watanabe K, Wanatabe S, Tsubata S, Uese K, Hashimoto I, Ichida F, Nakazawa M, Roth J, Miyawaki T. Hirono K, et al. Among authors: ichida f. J Am Coll Cardiol. 2006 Sep 19;48(6):1257-64. doi: 10.1016/j.jacc.2006.02.077. Epub 2006 Aug 28. J Am Coll Cardiol. 2006. PMID: 16979015 Free article.
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
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
Clinical features of adult patients with Eisenmenger's syndrome in Japan and Korea.
Sakazaki H, Niwa K, Nakazawa M, Saji T, Nakanishi T, Takamuro M, Ueno M, Kato H, Takatsuki S, Matsushima M, Kojima N, Ichida F, Kogaki S, Kido S, Arakaki Y, Waki K, Akagi T, Joo K, Muneuchi J, Suda K, Lee HJ, Shintaku H. Sakazaki H, et al. Among authors: ichida f. Int J Cardiol. 2013 Jul 15;167(1):205-9. doi: 10.1016/j.ijcard.2011.12.030. Epub 2012 Jan 9. Int J Cardiol. 2013. PMID: 22227251
Efficacy of immunoglobulin plus prednisolone for prevention of coronary artery abnormalities in severe Kawasaki disease (RAISE study): a randomised, open-label, blinded-endpoints trial.
Kobayashi T, Saji T, Otani T, Takeuchi K, Nakamura T, Arakawa H, Kato T, Hara T, Hamaoka K, Ogawa S, Miura M, Nomura Y, Fuse S, Ichida F, Seki M, Fukazawa R, Ogawa C, Furuno K, Tokunaga H, Takatsuki S, Hara S, Morikawa A; RAISE study group investigators. Kobayashi T, et al. Among authors: ichida f. Lancet. 2012 Apr 28;379(9826):1613-20. doi: 10.1016/S0140-6736(11)61930-2. Epub 2012 Mar 8. Lancet. 2012. PMID: 22405251 Clinical Trial.
340 results