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

Non-invasive three-dimensional electrical activation mapping to predict cardiac resynchronization therapy response: site of latest left ventricular activation relative to pacing site

利用无创三维电激活标测预测心脏再同步治疗反应:左心室最新激活部位相对于起搏部位的位置

Parreira, Leonor; Tsyganov, Alexey; Artyukhina, Elena; Vernooy, Kevin; Tondo, Claudio; Adragao, Pedro; Ascione, Ciro; Carmo, Pedro; Carvalho, Salomé; Egger, Matthias; Ferreira, Antonio; Ghossein, Mohammed; Holm, Magnus; Kalinin, Vitaly; Malakhova, Maria; Meine, Mathias; Nunes, Silvia; Podolyak, Dmitry; Revishvili, Amiran; Shapieva, Albina; Stepanova, Vera; van Stipdonk, Antonius; Taymasova, Irina; Wouters, Philippe; Zubarev, Stepan; Leyva, Francisco; Auricchio, Angelo; Varma, Niraj

Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome

对俄罗斯布鲁加达综合征患者中编码Nav1.5通道基因的诊断率和变异重新评估

Zaklyazminskaya, Elena; Shestak, Anna; Podolyak, Dmitry; Komoliatova, Vera; Makarov, Leonid; Novitskaya, Anna; Revishvili, Amiran

Variable Clinical Appearance of the Kir2.1 Rare Variants in Russian Patients with Long QT Syndrome

俄罗斯长 QT 综合征患者 Kir2.1 罕见变异的临床表现各异

Elena Zaklyazminskaya, Margarita Polyak, Anna Shestak, Mariam Sadekova, Vera Komoliatova, Irina Kiseleva, Leonid Makarov, Dmitriy Podolyak, Grigory Glukhov, Han Zhang, Denis Abramochkin, Olga S Sokolova

Viral rhodopsins 1 are an unique family of light-gated cation channels

病毒视紫红质1是一类独特的光控阳离子通道。

Dmitrii Zabelskii,Alexey Alekseev,Kirill Kovalev,Vladan Rankovic,Taras Balandin,Dmytro Soloviov,Dmitry Bratanov,Ekaterina Savelyeva,Elizaveta Podolyak,Dmytro Volkov,Svetlana Vaganova,Roman Astashkin,Igor Chizhov,Natalia Yutin,Maksim Rulev,Alexander Popov,Ana-Sofia Eria-Oliveira,Tatiana Rokitskaya,Thomas Mager,Yuri Antonenko,Riccardo Rosselli,Grigoriy Armeev,Konstantin Shaitan,Michel Vivaudou,Georg Büldt,Andrey Rogachev,Francisco Rodriguez-Valera,Mikhail Kirpichnikov,Tobias Moser,Andreas Offenhäusser,Dieter Willbold,Eugene Koonin,Ernst Bamberg,Valentin Gordeliy

Compound heterozygous mutations in KCNJ2 and KCNH2 in a patient with severe Andersen-Tawil syndrome

一名患有严重安德森-塔维尔综合征的患者携带KCNJ2和KCNH2基因的复合杂合突变

Polyak, Margarita E; Shestak, Anna; Podolyak, Dmitriy; Zaklyazminskaya, Elena