Kimura A - Search Results

1

Dilated phase of hypertrophic cardiomyopathy caused by two different sarcomere mutations, treated with surgical left ventricular reconstruction and cardiac resynchronization therapy with a defibrillator.

Sato A, Sakamoto N, Ando K, Kaneshiro T, Uekita H, Sugimoto K, Yamaki T, Kunii H, Nakazato K, Suzuki H, Saitoh S, Sato M, Tamagawa K, Arimura T, Kimura A, Takeishi Y. Sato A, et al. Among authors: kimura a. Intern Med. 2012;51(18):2559-64. doi: 10.2169/internalmedicine.51.7684. Epub 2012 Sep 15. Intern Med. 2012. PMID: 22989827 Free article.

2

Familial hypertrophic obstructive cardiomyopathy with the GLA E66Q mutation and zebra body.

Oikawa M, Sakamoto N, Kobayashi A, Suzuki S, Yoshihisa A, Yamaki T, Nakazato K, Suzuki H, Saitoh S, Kiko Y, Nakano H, Hayashi T, Kimura A, Takeishi Y. Oikawa M, et al. Among authors: kimura a. BMC Cardiovasc Disord. 2016 May 10;16:83. doi: 10.1186/s12872-016-0262-y. BMC Cardiovasc Disord. 2016. PMID: 27160240 Free PMC article.

3

Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes.

Arimura T, Ishikawa T, Nunoda S, Kawai S, Kimura A. Arimura T, et al. Among authors: kimura a. Hum Mutat. 2011 Dec;32(12):1481-91. doi: 10.1002/humu.21603. Epub 2011 Sep 29. Hum Mutat. 2011. PMID: 21898660

4

Screening of sarcomere gene mutations in young athletes with abnormal findings in electrocardiography: identification of a MYH7 mutation and MYBPC3 mutations.

Kadota C, Arimura T, Hayashi T, Naruse TK, Kawai S, Kimura A. Kadota C, et al. Among authors: kimura a. J Hum Genet. 2015 Oct;60(10):641-5. doi: 10.1038/jhg.2015.81. Epub 2015 Jul 16. J Hum Genet. 2015. PMID: 26178432 Clinical Trial.

5

Hypertrophic Cardiomyopathy Accompanied by Spinocerebellar Atrophy With a Novel Mutation in Troponin I Gene.

Kawai H, Morimoto S, Takakuwa Y, Ueda A, Inada K, Sarai M, Arimura T, Mutoh T, Kimura A, Ozaki Y. Kawai H, et al. Among authors: kimura a. Int Heart J. 2016 Jul 27;57(4):507-10. doi: 10.1536/ihj.15-444. Epub 2016 Jul 7. Int Heart J. 2016. PMID: 27385602 Free article.

6

Structural analysis of obscurin gene in hypertrophic cardiomyopathy.

Arimura T, Matsumoto Y, Okazaki O, Hayashi T, Takahashi M, Inagaki N, Hinohara K, Ashizawa N, Yano K, Kimura A. Arimura T, et al. Among authors: kimura a. Biochem Biophys Res Commun. 2007 Oct 19;362(2):281-7. doi: 10.1016/j.bbrc.2007.07.183. Epub 2007 Aug 13. Biochem Biophys Res Commun. 2007. PMID: 17716621

7

Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy.

Arimura T, Hayashi YK, Murakami T, Oya Y, Funabe S, Arikawa-Hirasawa E, Hattori N, Nishino I, Kimura A. Arimura T, et al. Among authors: kimura a. Circ J. 2009 Jan;73(1):158-61. doi: 10.1253/circj.cj-08-0722. Epub 2008 Nov 17. Circ J. 2009. PMID: 19015585 Free article.

8

Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy.

Arimura T, Bos JM, Sato A, Kubo T, Okamoto H, Nishi H, Harada H, Koga Y, Moulik M, Doi YL, Towbin JA, Ackerman MJ, Kimura A. Arimura T, et al. Among authors: kimura a. J Am Coll Cardiol. 2009 Jul 21;54(4):334-42. doi: 10.1016/j.jacc.2008.12.082. J Am Coll Cardiol. 2009. PMID: 19608031 Free article.

9

Genetic screening and double mutation in Japanese patients with hypertrophic cardiomyopathy.

Kubo T, Kitaoka H, Okawa M, Baba Y, Hirota T, Hayato K, Yamasaki N, Matsumura Y, Otsuka H, Arimura T, Kimura A, Doi YL. Kubo T, et al. Among authors: kimura a. Circ J. 2011;75(11):2654-9. doi: 10.1253/circj.cj-10-1314. Epub 2011 Jul 29. Circ J. 2011. PMID: 21799269 Free article. Clinical Trial.

10

Dilated cardiomyopathy-linked heat shock protein family D member 1 mutations cause up-regulation of reactive oxygen species and autophagy through mitochondrial dysfunction.

Enomoto H, Mittal N, Inomata T, Arimura T, Izumi T, Kimura A, Fukuda K, Makino S. Enomoto H, et al. Among authors: kimura a. Cardiovasc Res. 2021 Mar 21;117(4):1118-1131. doi: 10.1093/cvr/cvaa158. Cardiovasc Res. 2021. PMID: 32520982

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