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

Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation

长QT间期综合征:治疗开始后重新评估心律失常风险的重要性

Dusi, Veronica; Dagradi, Federica; Spazzolini, Carla; Crotti, Lia; Cerea, Paolo; Giovenzana, Fulvio L F; Musu, Giulia; Pedrazzini, Matteo; Torchio, Margherita; Schwartz, Peter J

Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients

心律失常性心肌病患者罕见和常见基因变异谱

Lippi, Melania; Chiesa, Mattia; Ascione, Ciro; Pedrazzini, Matteo; Mushtaq, Saima; Rovina, Davide; Riggio, Daniela; Di Blasio, Anna Maria; Biondi, Maria Luisa; Pompilio, Giulio; Colombo, Gualtiero I; Casella, Michela; Novelli, Valeria; Sommariva, Elena

Mutation location and IKs regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region

长QT综合征1型心律失常风险中的突变位点和IKs调控:KCNQ1 S6区的重要性

Schwartz, Peter J; Moreno, Cristina; Kotta, Maria-Christina; Pedrazzini, Matteo; Crotti, Lia; Dagradi, Federica; Castelletti, Silvia; Haugaa, Kristina H; Denjoy, Isabelle; Shkolnikova, Maria A; Brink, Paul A; Heradien, Marshall J; Seyen, Sandrine R M; Spätjens, Roel L H M G; Spazzolini, Carla; Volders, Paul G A

MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes

MTMR4 SNVs 调控先天性长QT综合征中的离子通道降解和临床严重程度:对保护性修饰基因作用机制的深入理解

Lee, Yee-Ki; Sala, Luca; Mura, Manuela; Rocchetti, Marcella; Pedrazzini, Matteo; Ran, Xinru; Mak, Timothy S H; Crotti, Lia; Sham, Pak C; Torre, Eleonora; Zaza, Antonio; Schwartz, Peter J; Tse, Hung-Fat; Gnecchi, Massimiliano

Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants

估计罕见KCNH2变异体患长QT综合征的后验概率

Kozek, Krystian; Wada, Yuko; Sala, Luca; Denjoy, Isabelle; Egly, Christian; O'Neill, Matthew J; Aiba, Takeshi; Shimizu, Wataru; Makita, Naomasa; Ishikawa, Taisuke; Crotti, Lia; Spazzolini, Carla; Kotta, Maria-Christina; Dagradi, Federica; Castelletti, Silvia; Pedrazzini, Matteo; Gnecchi, Massimiliano; Leenhardt, Antoine; Salem, Joe-Elie; Ohno, Seiko; Zuo, Yi; Glazer, Andrew M; Mosley, Jonathan D; Roden, Dan M; Knollmann, Bjorn C; Blume, Jeffrey D; Extramiana, Fabrice; Schwartz, Peter J; Horie, Minoru; Kroncke, Brett M

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

跨种族全基因组关联研究揭示长QT综合征的遗传结构和遗传性

Lahrouchi, Najim; Tadros, Rafik; Crotti, Lia; Mizusawa, Yuka; Postema, Pieter G; Beekman, Leander; Walsh, Roddy; Hasegawa, Kanae; Barc, Julien; Ernsting, Marko; Turkowski, Kari L; Mazzanti, Andrea; Beckmann, Britt M; Shimamoto, Keiko; Diamant, Ulla-Britt; Wijeyeratne, Yanushi D; Kucho, Yu; Robyns, Tomas; Ishikawa, Taisuke; Arbelo, Elena; Christiansen, Michael; Winbo, Annika; Jabbari, Reza; Lubitz, Steven A; Steinfurt, Johannes; Rudic, Boris; Loeys, Bart; Shoemaker, M Ben; Weeke, Peter E; Pfeiffer, Ryan; Davies, Brianna; Andorin, Antoine; Hofman, Nynke; Dagradi, Federica; Pedrazzini, Matteo; Tester, David J; Bos, J Martijn; Sarquella-Brugada, Georgia; Campuzano, Óscar; Platonov, Pyotr G; Stallmeyer, Birgit; Zumhagen, Sven; Nannenberg, Eline A; Veldink, Jan H; van den Berg, Leonard H; Al-Chalabi, Ammar; Shaw, Christopher E; Shaw, Pamela J; Morrison, Karen E; Andersen, Peter M; Müller-Nurasyid, Martina; Cusi, Daniele; Barlassina, Cristina; Galan, Pilar; Lathrop, Mark; Munter, Markus; Werge, Thomas; Ribasés, Marta; Aung, Tin; Khor, Chiea C; Ozaki, Mineo; Lichtner, Peter; Meitinger, Thomas; van Tintelen, J Peter; Hoedemaekers, Yvonne; Denjoy, Isabelle; Leenhardt, Antoine; Napolitano, Carlo; Shimizu, Wataru; Schott, Jean-Jacques; Gourraud, Jean-Baptiste; Makiyama, Takeru; Ohno, Seiko; Itoh, Hideki; Krahn, Andrew D; Antzelevitch, Charles; Roden, Dan M; Saenen, Johan; Borggrefe, Martin; Odening, Katja E; Ellinor, Patrick T; Tfelt-Hansen, Jacob; Skinner, Jonathan R; van den Berg, Maarten P; Olesen, Morten Salling; Brugada, Josep; Brugada, Ramón; Makita, Naomasa; Breckpot, Jeroen; Yoshinaga, Masao; Behr, Elijah R; Rydberg, Annika; Aiba, Takeshi; Kääb, Stefan; Priori, Silvia G; Guicheney, Pascale; Tan, Hanno L; Newton-Cheh, Christopher; Ackerman, Michael J; Schwartz, Peter J; Schulze-Bahr, Eric; Probst, Vincent; Horie, Minoru; Wilde, Arthur A; Tanck, Michael W T; Bezzina, Connie R

The genetics underlying acquired long QT syndrome: impact for genetic screening

获得性长QT间期综合征的遗传学基础:对基因筛查的影响

Itoh, Hideki; Crotti, Lia; Aiba, Takeshi; Spazzolini, Carla; Denjoy, Isabelle; Fressart, Véronique; Hayashi, Kenshi; Nakajima, Tadashi; Ohno, Seiko; Makiyama, Takeru; Wu, Jie; Hasegawa, Kanae; Mastantuono, Elisa; Dagradi, Federica; Pedrazzini, Matteo; Yamagishi, Masakazu; Berthet, Myriam; Murakami, Yoshitaka; Shimizu, Wataru; Guicheney, Pascale; Schwartz, Peter J; Horie, Minoru

JAK2 exon 14 skipping in patients with primary myelofibrosis: a minor splice variant modulated by the JAK2-V617F allele burden.

原发性骨髓纤维化患者的 JAK2 外显子 14 跳跃:一种受 JAK2-V617F 等位基因负荷调节的次要剪接变体

Catarsi Paolo, Rosti Vittorio, Morreale Giacomo, Poletto Valentina, Villani Laura, Bertorelli Roberto, Pedrazzini Matteo, Zorzetto Michele, Barosi Giovanni

Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel

由严重功能障碍的心脏钠通道引起的长QT间期综合征恶性围产期变异型

Wang, Dao W; Crotti, Lia; Shimizu, Wataru; Pedrazzini, Matteo; Cantu, Francesco; De Filippo, Paolo; Kishiki, Kanako; Miyazaki, Aya; Ikeda, Tomoaki; Schwartz, Peter J; George, Alfred L Jr

Cardiac potassium channel dysfunction in sudden infant death syndrome

婴儿猝死综合征中的心脏钾通道功能障碍

Rhodes, Troy E; Abraham, Robert L; Welch, Richard C; Vanoye, Carlos G; Crotti, Lia; Arnestad, Marianne; Insolia, Roberto; Pedrazzini, Matteo; Ferrandi, Chiara; Vege, Ashild; Rognum, Torleiv; Roden, Dan M; Schwartz, Peter J; George, Alfred L Jr