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Page 1
Identification of transmembrane protein 168 mutation in familial Brugada syndrome.
Shimizu A, Zankov DP, Sato A, Komeno M, Toyoda F, Yamazaki S, Makita T, Noda T, Ikawa M, Asano Y, Miyashita Y, Takashima S, Morita H, Ishikawa T, Makita N, Hitosugi M, Matsuura H, Ohno S, Horie M, Ogita H. Shimizu A, et al. Among authors: morita h. FASEB J. 2020 May;34(5):6399-6417. doi: 10.1096/fj.201902991R. Epub 2020 Mar 16. FASEB J. 2020. PMID: 32175648
Atrial fibrillation in patients with Brugada syndrome relationships of gene mutation, electrophysiology, and clinical backgrounds.
Kusano KF, Taniyama M, Nakamura K, Miura D, Banba K, Nagase S, Morita H, Nishii N, Watanabe A, Tada T, Murakami M, Miyaji K, Hiramatsu S, Nakagawa K, Tanaka M, Miura A, Kimura H, Fuke S, Sumita W, Sakuragi S, Urakawa S, Iwasaki J, Ohe T. Kusano KF, et al. Among authors: morita h. J Am Coll Cardiol. 2008 Mar 25;51(12):1169-75. doi: 10.1016/j.jacc.2007.10.060. J Am Coll Cardiol. 2008. PMID: 18355654 Free article.
Abnormal transmural repolarization process in patients with Brugada syndrome.
Sangawa M, Morita H, Nakatsu T, Nishii N, Miura D, Miura A, Tada T, Murakami M, Hiramatsu S, Nagase S, Nakamura K, Oka T, Toyonaga S, Mashima K, Kusachi S, Yamamoto K, Ohe T, Kusano KF. Sangawa M, et al. Among authors: morita h. Heart Rhythm. 2009 Aug;6(8):1163-9. doi: 10.1016/j.hrthm.2009.04.037. Epub 2009 May 4. Heart Rhythm. 2009. PMID: 19632628
Abnormal restitution property of action potential duration and conduction delay in Brugada syndrome: both repolarization and depolarization abnormalities.
Nishii N, Nagase S, Morita H, Kusano KF, Namba T, Miura D, Miyaji K, Hiramatsu S, Tada T, Murakami M, Watanabe A, Banba K, Sakai Y, Nakamura K, Oka T, Ohe T. Nishii N, et al. Among authors: morita h. Europace. 2010 Apr;12(4):544-52. doi: 10.1093/europace/eup432. Epub 2010 Jan 17. Europace. 2010. PMID: 20083482
Elevated oxidative stress is associated with ventricular fibrillation episodes in patients with Brugada-type electrocardiogram without SCN5A mutation.
Tanaka M, Nakamura K, Kusano KF, Morita H, Ohta-Ogo K, Miura D, Miura A, Nakagawa K, Tada T, Murakami M, Nishii N, Nagase S, Hata Y, Kohno K, Ouchida M, Shimizu K, Yutani C, Ohe T, Ito H. Tanaka M, et al. Among authors: morita h. Cardiovasc Pathol. 2011 Jan-Feb;20(1):e37-42. doi: 10.1016/j.carpath.2010.02.002. Epub 2010 Mar 12. Cardiovasc Pathol. 2011. PMID: 20219395
Efficacy of low-dose bepridil for prevention of ventricular fibrillation in patients with Brugada syndrome with and without SCN5A mutation.
Murakami M, Nakamura K, Kusano KF, Morita H, Nakagawa K, Tanaka M, Tada T, Toh N, Nishii N, Nagase S, Hata Y, Kohno K, Miura D, Ohe T, Ito H. Murakami M, et al. Among authors: morita h. J Cardiovasc Pharmacol. 2010 Oct;56(4):389-95. doi: 10.1097/FJC.0b013e3181f03c2f. J Cardiovasc Pharmacol. 2010. PMID: 20625312 Clinical Trial.
SCN5A mutation is associated with early and frequent recurrence of ventricular fibrillation in patients with Brugada syndrome.
Nishii N, Ogawa M, Morita H, Nakamura K, Banba K, Miura D, Kumagai N, Matsunaga A, Kawamura H, Urakawa S, Miyaji K, Nagai M, Satoh K, Nakagawa K, Tanaka M, Hiramatsu S, Tada T, Murakami M, Nagase S, Kohno K, Kusano KF, Saku K, Ohe T, Ito H. Nishii N, et al. Among authors: morita h. Circ J. 2010 Nov;74(12):2572-8. doi: 10.1253/circj.cj-10-0445. Epub 2010 Oct 30. Circ J. 2010. PMID: 21048329 Free article.
2,839 results