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Page 1
Mexiletine shortens the QT interval in a pedigree of KCNH2 related long QT syndrome.
Fujisawa T, Aizawa Y, Katsumata Y, Kimura K, Hashimoto K, Yamashita T, Miyama H, Kimura T, Kosaki K, Takatsuki S, Shimizu W, Fukuda K. Fujisawa T, et al. Among authors: kosaki k. J Arrhythm. 2020 Jan 8;36(1):193-196. doi: 10.1002/joa3.12300. eCollection 2020 Feb. J Arrhythm. 2020. PMID: 32071644 Free PMC article.
Coexistence of two distinct fascinating cardiovascular disorders: heterotaxy syndrome with left ventricular non-compaction and vasospastic angina.
Egashira T, Yuasa S, Kimura M, Sawano M, Anzai A, Hayashida K, Kawamura A, Kimura T, Nishiyama N, Aizawa Y, Takatsuki S, Tsuruta H, Murata M, Yamada Y, Kohno T, Maekawa Y, Sano M, Kosaki K, Fukuda K. Egashira T, et al. Among authors: kosaki k. Int J Cardiol. 2014 Jun 15;174(2):e54-6. doi: 10.1016/j.ijcard.2014.04.032. Epub 2014 Apr 15. Int J Cardiol. 2014. PMID: 24768391 No abstract available.
An RyR2 mutation found in a family with a short-coupled variant of torsade de pointes.
Kimura M, Fujisawa T, Aizawa Y, Matsuhashi N, Ito S, Nakajima K, Kashimura S, Kunitomi A, Katsumata Y, Nishiyama T, Kimura T, Nishiyama N, Yuasa S, Takatsuki S, Kosaki K, Fukuda K. Kimura M, et al. Among authors: kosaki k. Int J Cardiol. 2017 Jan 15;227:367-369. doi: 10.1016/j.ijcard.2016.11.052. Epub 2016 Nov 8. Int J Cardiol. 2017. PMID: 27839804 No abstract available.
A genome-wide association analysis identifies PDE1A|DNAJC10 locus on chromosome 2 associated with idiopathic pulmonary arterial hypertension in a Japanese population.
Kimura M, Tamura Y, Guignabert C, Takei M, Kosaki K, Tanabe N, Tatsumi K, Saji T, Satoh T, Kataoka M, Kamitsuji S, Kamatani N, Thuillet R, Tu L, Humbert M, Fukuda K, Sano M. Kimura M, et al. Among authors: kosaki k. Oncotarget. 2017 Aug 24;8(43):74917-74926. doi: 10.18632/oncotarget.20459. eCollection 2017 Sep 26. Oncotarget. 2017. PMID: 29088834 Free PMC article.
SOX17 Mutations in Japanese Patients with Pulmonary Arterial Hypertension.
Hiraide T, Kataoka M, Suzuki H, Aimi Y, Chiba T, Kanekura K, Satoh T, Fukuda K, Gamou S, Kosaki K. Hiraide T, et al. Among authors: kosaki k. Am J Respir Crit Care Med. 2018 Nov 1;198(9):1231-1233. doi: 10.1164/rccm.201804-0766LE. Am J Respir Crit Care Med. 2018. PMID: 30044643 No abstract available.
Development of monomorphic ventricular tachycardia in a patient with fever-induced Brugada syndrome.
Sato Y, Aizawa Y, Fujisawa T, Ito S, Katano K, Fuse N, Miyabe A, Osada K, Ishihara R, Tosaka A, Tamamura T, Mizumura T, Sugimura Y, Nakajima K, Katsumata Y, Nishiyama T, Kimura T, Furukawa Y, Takatsuki S, Kosaki K, Fukuda K. Sato Y, et al. Among authors: kosaki k. J Arrhythm. 2018 Jun 4;34(4):465-468. doi: 10.1002/joa3.12068. eCollection 2018 Aug. J Arrhythm. 2018. PMID: 30167021 Free PMC article.
Sex-Dependent Phenotypic Variability of an SCN5A Mutation: Brugada Syndrome and Sick Sinus Syndrome.
Aizawa Y, Fujisawa T, Katsumata Y, Kohsaka S, Kunitomi A, Ohno S, Sonoda K, Hayashi H, Hojo R, Fukamizu S, Nagase S, Ito S, Nakajima K, Nishiyama T, Kimura T, Kurita Y, Furukawa Y, Takatsuki S, Ogawa S, Nakazato Y, Sumiyoshi M, Kosaki K, Horie M, Fukuda K. Aizawa Y, et al. Among authors: kosaki k. J Am Heart Assoc. 2018 Sep 18;7(18):e009387. doi: 10.1161/JAHA.118.009387. J Am Heart Assoc. 2018. PMID: 30371189 Free PMC article.
A Homozygous CASQ2 Mutation in a Japanese Patient with Catecholaminergic Polymorphic Ventricular Tachycardia.
Fujisawa T, Aizawa Y, Katsumata Y, Udo A, Ito S, Hatakeyama K, Hirose M, Miyama H, Nakajima K, Nishiyama T, Kimura T, Nitta M, Misumi K, Takatsuki S, Kosaki K, Fukuda K. Fujisawa T, et al. Among authors: kosaki k. Case Rep Genet. 2019 Jan 8;2019:9056596. doi: 10.1155/2019/9056596. eCollection 2019. Case Rep Genet. 2019. PMID: 30729048 Free PMC article.
537 results