日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Flecainide Is Associated With a Lower Incidence of Arrhythmic Events in a Large Cohort of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

在一项针对大量儿茶酚胺敏感性多形性室性心动过速患者的研究中,氟卡尼与较低的心律失常事件发生率相关。

Bergeman, Auke T; Lieve, Krystien V V; Kallas, Dania; Bos, J Martijn; Rosés I Noguer, Ferran; Denjoy, Isabelle; Zorio, Esther; Kammeraad, Janneke A E; Peltenburg, Puck J; Tobert, Katie; Aiba, Takeshi; Atallah, Joseph; Drago, Fabrizio; Batra, Anjan S; Brugada, Ramon; Borggrefe, Martin; Clur, Sally-Ann B; Cox, Moniek G P J; Davis, Andrew; Dhillon, Santokh; Etheridge, Susan P; Fischbach, Peter; Franciosi, Sonia; Haugaa, Kristina; Horie, Minoru; Johnsrude, Christopher; Kane, Austin M; Krause, Ulrich; Kwok, Sit-Yee; LaPage, Martin J; Ohno, Seiko; Probst, Vincent; Roberts, Jason D; Robyns, Tomas; Sacher, Frederic; Semsarian, Christopher; Skinner, Jonathan R; Swan, Heikki; Tavacova, Terezia; Tisma-Dupanovic, Svjetlana; Tfelt-Hansen, Jacob; Yap, Sing-Chien; Kannankeril, Prince J; Leenhardt, Antoine; Till, Janice; Sanatani, Shubhayan; Tanck, Michael W T; Ackerman, Michael J; Wilde, Arthur A M; van der Werf, Christian

Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation.

由兰尼碱受体 2 型 P2328S 突变引起的儿茶酚胺能多形性室性心动过速的谱系和临床过程

Koponen Mikael, Marjamaa Annukka, Tuiskula Annukka M, Viitasalo Matti, Nallinmaa-Luoto Terhi, Leinonen Jaakko T, Widen Elisabeth, Toivonen Lauri, Kontula Kimmo, Swan Heikki

Heritability in genetic heart disease: the role of genetic background

遗传性心脏病的遗传性:遗传背景的作用

Jansweijer, Joeri A; van Spaendonck-Zwarts, Karin Y; Tanck, Michael W T; van Tintelen, J Peter; Christiaans, Imke; van der Smagt, Jasper; Vermeer, Alexa; Bos, J Martijn; Moss, Arthur J; Swan, Heikki; Priori, Sylvia G; Rydberg, Annika; Tfelt-Hansen, Jacob; Ackerman, Michael J; Olivotto, Iacopo; Charron, Philippe; Gimeno, Juan R; van den Berg, Maarten; Wilde, Arthur A M; Pinto, Yigal M

The Role of KCNQ1 Mutations and Maternal Beta Blocker Use During Pregnancy in the Growth of Children With Long QT Syndrome

KCNQ1基因突变和孕期母体使用β受体阻滞剂对长QT综合征患儿生长发育的影响

Huttunen, Heta; Hero, Matti; Lääperi, Mitja; Känsäkoski, Johanna; Swan, Heikki; Hirsch, Joel A; Miettinen, Päivi J; Raivio, Taneli

Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients

成人长QT综合征1型和2型患者的临床和分子遗传风险决定因素:Koponen等人对成人长QT综合征患者的随访

Koponen, Mikael; Havulinna, Aki S; Marjamaa, Annukka; Tuiskula, Annukka M; Salomaa, Veikko; Laitinen-Forsblom, Päivi J; Piippo, Kirsi; Toivonen, Lauri; Kontula, Kimmo; Viitasalo, Matti; Swan, Heikki

Comparison of QT peak and QT end interval responses to autonomic adaptation in asymptomatic LQT1 mutation carriers

无症状LQT1突变携带者自主神经适应后QT峰值和QT末期反应的比较

Haapalahti, Petri; Viitasalo, Matti; Perhonen, Merja; Väänänen, Heikki; Mäkijärvi, Markku; Swan, Heikki; Toivonen, Lauri

KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome?

KCNE1 D85N多态性——1型长QT综合征的性别特异性修饰因子?

Lahtinen, Annukka M; Marjamaa, Annukka; Swan, Heikki; Kontula, Kimmo

Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia

在类似儿茶酚胺敏感性多形性室性心动过速的家族性室性心律失常中寻找心脏钙循环基因突变

Marjamaa, Annukka; Laitinen-Forsblom, Päivi; Lahtinen, Annukka M; Viitasalo, Matti; Toivonen, Lauri; Kontula, Kimmo; Swan, Heikki

High prevalence of four long QT syndrome founder mutations in the Finnish population

芬兰人群中四种长QT综合征创始突变的高发率

Marjamaa, Annukka; Salomaa, Veikko; Newton-Cheh, Christopher; Porthan, Kimmo; Reunanen, Antti; Karanko, Hannu; Jula, Antti; Lahermo, Päivi; Väänänen, Heikki; Toivonen, Lauri; Swan, Heikki; Viitasalo, Matti; Nieminen, Markku S; Peltonen, Leena; Oikarinen, Lasse; Palotie, Aarno; Kontula, Kimmo

Reproducibility of computerized measurements of QT interval from multiple leads at rest and during exercise

静息和运动状态下多导联QT间期计算机测量的可重复性

Hekkala, Anna-Mari; Väänänen, Heikki; Swan, Heikki; Oikarinen, Lasse; Viitasalo, Matti; Toivonen, Lauri