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Page 1
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.
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.
Truncating mutation in CSNK2B and myoclonic epilepsy.
Sakaguchi Y, Uehara T, Suzuki H, Kosaki K, Takenouchi T. Sakaguchi Y, et al. Among authors: kosaki k. Hum Mutat. 2017 Nov;38(11):1611-1612. doi: 10.1002/humu.23307. Epub 2017 Sep 14. Hum Mutat. 2017. PMID: 28762608 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.
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.
538 results