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

Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study

Nexilin (NEXN) 相关性心肌病的遗传和表型特征:一项多中心研究的结果

Perotto, Maria; Paldino, Alessia; Mazzarotto, Francesco; Barbati, Giulia; Stroeks, Sophie L V M; Verdonschot, Job A J; Akhtar, Mohammed; Elliott, Perry; Ochoa, Juan Pablo; Garcia-Pavia, Pablo; de Frutos, Fernando; Sepp, Robert; Hategan, Lidia; Prasad, Sanjay; Yazdani, Momina; Morris-Rosendahl, Deborah; Palinkas, Eszter Dalma; Girolami, Francesca; Olivotto, Iacopo; Parikh, Victoria N; Fatkin, Diane; Lakdawala, Neal; McKenna, William J; Stolfo, Davide; Gigli, Marta; Brun, Francesca; Collesi, Chiara; Giacca, Mauro; Zacchigna, Serena; Severini, Giovanni Maria; Lenarduzzi, Stefania; Spedicati, Beatrice; Santin, Aurora; Girotto, Giorgia; Gasparini, Paolo; Taylor, Matthew R G; Mestroni, Luisa; Merlo, Marco; Sinagra, Gianfranco; Dal Ferro, Matteo

Magnetic Resonance Imaging Characterization and Clinical Outcomes of Dilated and Arrhythmogenic Left Ventricular Cardiomyopathies

扩张型和致心律失常性左心室心肌病的磁共振成像特征及临床结局

Castrichini, Matteo; De Luca, Antonio; De Angelis, Giulia; Neves, Raquel; Paldino, Alessia; Dal Ferro, Matteo; Barbati, Giulia; Medo, Kristen; Barison, Andrea; Grigoratos, Chrysanthos; Gigli, Marta; Stolfo, Davide; Brun, Francesca; Groves, Daniel W; Quaife, Robert; Eldemire, Ramone; Graw, Sharon; Addison, Jeffrey; Todiere, Giancarlo; Gueli, Ignazio Alessio; Botto, Nicoletta; Emdin, Michele; Aquaro, Giovanni Donato; Garmany, Ramin; Pereira, Naveen L; Taylor, Matthew R G; Ackerman, Michael J; Sinagra, Gianfranco; Mestroni, Luisa; Giudicessi, John R; Merlo, Marco

Impact of DCM-Causing Genetic Background on Long-Term Response to Cardiac Resynchronization Therapy

导致扩张型心肌病(DCM)的遗传背景对心脏再同步治疗长期疗效的影响

Dal Ferro, Matteo; Paldino, Alessia; Gregorio, Caterina; Bessi, Riccardo; Zaffalon, Denise; De Angelis, Giulia; Severini, Giovanni Maria; Stolfo, Davide; Gigli, Marta; Brun, Francesca; Massa, Laura; Korcova, Renata; Salvatore, Luca; Bianco, Elisabetta; Mestroni, Luisa; Merlo, Marco; Zecchin, Massimo; Sinagra, Gianfranco

Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants

由丝状蛋白C截短变异体引起的心肌病的表型表达、自然史和风险分层

Gigli, Marta; Stolfo, Davide; Graw, Sharon L; Merlo, Marco; Gregorio, Caterina; Nee Chen, Suet; Dal Ferro, Matteo; PaldinoMD, Alessia; De Angelis, Giulia; Brun, Francesca; Jirikowic, Jean; Salcedo, Ernesto E; Turja, Sylvia; Fatkin, Diane; Johnson, Renee; van Tintelen, J Peter; Te Riele, Anneline S J M; Wilde, Arthur A M; Lakdawala, Neal K; Picard, Kermshlise; Miani, Daniela; Muser, Daniele; Maria Severini, Giovanni; Calkins, Hugh; James, Cynthia A; Murray, Brittney; Tichnell, Crystal; Parikh, Victoria N; Ashley, Euan A; Reuter, Chloe; Song, Jiangping; Judge, Daniel P; McKenna, William J; Taylor, Matthew R G; Sinagra, Gianfranco; Mestroni, Luisa

FLNC truncations cause arrhythmogenic right ventricular cardiomyopathy

FLNC截断可导致致心律失常性右室心肌病

Brun, Francesca; Gigli, Marta; Graw, Sharon L; Judge, Daniel P; Merlo, Marco; Murray, Brittney; Calkins, Hugh; Sinagra, Gianfranco; Taylor, Matthew Rg; Mestroni, Luisa; James, Cynthia A

Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis.

对致心律失常性右室发育不良/心肌病中 SCN5A 突变的多层次分析表明,疾病发病机制存在非经典机制

Te Riele Anneline S J M, Agullo-Pascual Esperanza, James Cynthia A, Leo-Macias Alejandra, Cerrone Marina, Zhang Mingliang, Lin Xianming, Lin Bin, Sobreira Nara L, Amat-Alarcon Nuria, Marsman Roos F, Murray Brittney, Tichnell Crystal, van der Heijden Jeroen F, Dooijes Dennis, van Veen Toon A B, Tandri Harikrishna, Fowler Steven J, Hauer Richard N W, Tomaselli Gordon, van den Berg Maarten P, Taylor Matthew R G, Brun Francesca, Sinagra Gianfranco, Wilde Arthur A M, Mestroni Luisa, Bezzina Connie R, Calkins Hugh, Peter van Tintelen J, Bu Lei, Delmar Mario, Judge Daniel P

Right precordial-directed electrocardiographical markers identify arrhythmogenic right ventricular cardiomyopathy in the absence of conventional depolarization or repolarization abnormalities

右胸前导联心电图标志物可在无常规去极化或复极化异常的情况下识别致心律失常性右室心肌病。

Cortez, Daniel; Svensson, Anneli; Carlson, Jonas; Graw, Sharon; Sharma, Nandita; Brun, Francesca; Spezzacatene, Anita; Mestroni, Luisa; Platonov, Pyotr G

Clinical Spectrum of PRKAG2 Syndrome

PRKAG2综合征的临床表现谱

Porto, Andrea Giuseppe; Brun, Francesca; Severini, Giovanni Maria; Losurdo, Pasquale; Fabris, Enrico; Taylor, Matthew R G; Mestroni, Luisa; Sinagra, Gianfranco

[Molecular genetic testing according to the latest European guidelines on hypertrophic cardiomyopathy]

[根据欧洲最新肥厚型心肌病指南进行分子遗传学检测]

Brun, Francesca; Mestroni, Luisa; Sinagra, Gianfranco