Results 1 to 10 of about 32,760 (223)

Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype. [PDF]

, 2019
BACKGROUND: Pathogenic variants in the filamin C (FLNC) gene are associated with inherited cardiomyopathies including dilated cardiomyopathy with an arrhythmogenic phenotype.
Aguilera, B, Akhtar, MM, Asimaki, A, Dalageorgou, C, Futema, M, Gimeno, JR, Hall, CL, Hernández, JP, McKenna, WJ, Molina, P, Pastor, F, Pittman, AM, Protonotarios, A, Sabater-Molina, M, Suarez, MP, Syrris, P, Zorio, E   +16 more
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Cardiosphere-derived cells suppress allogeneic lymphocytes by production of PGE2 acting via the EP4 receptor [PDF]

, 2018
derived cells (CDCs) are a cardiac progenitor cell population, which have been shown to possess cardiac regenerative properties and can improve heart function in a variety of cardiac diseases. Studies in large animal models have predominantly focussed on
A Augello, AJ Nauta, AJ Poncelet, AJ White, AS Boyd, B Hegyi, B Nadal-Ginard, C Basso, C Boriesson, C Liang, CH Chen, CY Xiao, D Carrade, D Pinheiro, DR Davis, DY Nah, E Ingulli, EM Oxford, G Couto de, G Wess, G Wess, GO Ramirez-Yañez, H Kanazawa, H Takeyama, I Chimenti, JA Dixon, JG Bartolucci, JM Angles, JW Kang, K Blanc Le, K Malliaras, K Malliaras, K Sato, KM Meurs, L Cambier, L Grigorian-Shamagian, L Lauden, L Öberg, LC Dutton, LJ Kennedy, M Haidar, MA Aminzadeh, MD Nicola, ME Bernardo, ME Campian, MM Duffy, MT Hensley, MT Hensley, N Kvirkvelia, O Campuzano, P Ross, PV Johnston, Q Guan, R Gallet, R Meisel, R Ramasamy, RR Makkar, S Aggarwal, S Simpson, SJ Jansen of Lorkeers, SR Houser, ST Lee, T Maślanka, TL Lynch, TS Li, WS Lee, Y Ding, Y Sun, YC Hsueh, Z Yan   +69 more
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Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence [PDF]

, 2016
Additional file 3: Figure S3. Regulation of genes of Arrhythmogenic right ventricular cardiomyopathy pathway during senescence induction in HFF strains Genes of the “Arrhythmogenic right ventricular cardiomyopathy” pathway which are significantly up ...
A Chicas, A Ciccia, A Iglesias-Ara, A Kaneda, A Leonardo Di, A Massoud, A Musio, A Ors, A Poehlmann, A Saadane, A Smogorzewska, A Ventura, A Zuryń, A Zuryń, AA Goodarzi, AB Parrish, AC Baege, AC Johansson, AJ Nakamura, AJT Millis, AM Havelka, AY Maslov, B Cen, B Pandit, B Zhivotovsky, BD Chang, Bernardes Jesus de, BP Kaistha, C Kenyon, C Michaloglou, C Morvan Le, C Rouault, C Sandhu, C Sidler, C Trapnell, CF Winter de, Christoph Kaether, CM Aliouat-Denis, D Bhaumik, D Coppola, D Lodygin, D Muthna, DA Alcorta, DH Lackner, DH Larsen, DJ Baker, DM Finucane, DN Shelton, DR Bentley, DR Wonsey, DW Chan, E Hara, E Natarajan, E Pazolli, EJ Gavin, ES Hwang, F Debacq-Chainiaux, F d’Adda di Fagagna, F Ling, F Rapaport, F Rodier, F Rodier, F Seyednasrollah, FA Mallette, G Thuret, GP Dimri, GP Dimri, GP Dimri, H Harada, H Takai, H Zalzali, HJ Kim, HJ Kim, I Androic, I Ben-Porath, I Ben-Porath, I Wierstra, IB Roninson, IK Yoon, IM Kim, IP Kovalchuk, J Bartkova, J Bunt, J Campisi, J Campisi, J Campisi, J Campisi, J Laoukili, J Manns, J Pawlowski, J Tomida, J Zhao, JC Acosta, JC Jeyapalan, JF Passos, JH Chen, JH Chen, JH Chin, JM Dhahbi, JM Yi, JP Carey, JP Coppé, JR Smith, JW Hofmann, JW Shay, K Itahana, K Johung, K Suzuki, K Voutetakis, KH Choi, KS Kim, L Gopinathan, L Hayflick, L Hirsch, L Jia, L Meng, L Zhang, M Blank, M Braig, M Collado, M Kronschnabl, M Narita, M Petric, M Purcell, M Serrano, MA Bonelli, Marco Groth, Matthias Platzer, MD Robinson, MI Love, MJ Smout, MK Ha, MK Kang, MT Paulsen, N Kikuchi, N Martin, N Ohtani, N Wajapeyee, NF Mathon, NG Berube, O Aksoy, O Toussaint, P Dekker, P Flicek, P Gupta, P Luo, P Sun, Peter Hemmerich, Q Gan, QF Wu, R Binet, R Mirzayans, R Mjelle, R Salama, RA Quadri, Reinhard Guthke, RJ Sabin, RT Abraham, S Anders, S Courtois-Cox, S Ferrando-Martinez, S Gonzalez, S Haupt, S Honda, S Hubackova, S Kim, S Lin, S Marthandan, S Marthandan, S Marthandan, S Marthandan, S Pollok, S Ressler, S Schäuble, S Sivakumar, S Vaughan, S Walter, Shiva Marthandan, SJ Robles, SP Linke, SP Mooijaart, SS Myatt, Steffen Priebe, Stephan Diekmann, T Chen, T Kaneko, T Kidokoro, T Kuilman, TC Kuilman, TV Kalin, U Herbig, Uwe Menzel, V Gire, VV Kalinichenko, W Cosme-Blanco, W Luo, W Wagner, W Xue, XW Cheng, Y Bai, Y Benjamini, Y Chien, Y Kong, Y Kotake, Y Ma, Y Nakayama, Y Takahashi, Y Tan, Y Zhang, YH Hsu, YJ Choi, YM Kim, Z Chen, Z Gong, Z Wang, Z Xie   +215 more
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Right ventricular assessment of the adolescent footballer’s heart

Echo Research and Practice
Introduction Athletic training can result in electrical and structural changes of the right ventricle that may mimic phenotypical features of arrhythmogenic right ventricular cardiomyopathy (ARVC), such as T-wave inversion and right heart dilatation.
D. X. Augustine, J. Willis, S. Sivalokanathan, C. Wild, A. Sharma, A. Zaidi, K. Pearce, G. Stuart, M. Papadakis, S. Sharma, A. Malhotra   +10 more
doaj   +1 more source

Diagnostic and prognostic roles of echocardiography and cardiac magnetic resonance [PDF]

, 2016
Cardiolog
Chiara Bucciarelli-Ducci, Jeroen J. Bax, Victoria Delgado   +2 more
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LV‐predominant arrhythmogenic cardiomyopathy related to pathogenic DSP‐variant

Clinical Case Reports
Key Clinical Message In contrast to previously thought, arrhythmogenic cardiomyopathy can occur exclusively in the left ventricle in association with autosomal dominant mutation, even without any skin manifestations.
Soban Ahmad, Husam El Sharu, Robin Fernandes, Mark Kolasa, Constantin Bogdan Marcu   +4 more
doaj   +1 more source

Catheter Ablation of Ventricular Tachycardia in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: A Sequential Approach

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2019
Background It has been suggested that endocardial and epicardial ablation of ventricular tachycardia (VT) improves outcome in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Shibu Mathew, Ardan M. Saguner, Niklas Schenker, Lukas Kaiser, Pengpai Zhang, Yoshiga Yashuiro, Christine Lemes, Thomas Fink, Tilman Maurer, Francesco Santoro, Peter Wohlmuth, Bruno Reißmann, Christian H. Heeger, Roland Tilz, Erik Wissner, Andreas Rillig, Andreas Metzner, Karl‐Heinz Kuck, Feifan Ouyang   +18 more
doaj   +1 more source

Rapid progression of right ventricular dysfunction: a case report

BMC Cardiovascular Disorders
Background Arrhythmogenic cardiomyopathy (ACM) is a genetic myocardial disease characterized by progressive myocyte loss and fibrofatty (fibrous and adipose) tissue replacement to predispose these patients to fatal ventricular arrhythmias and impairment ...
Guoliang Li, Changying Zhao, Lingmin Wu, Yang Yan   +3 more
doaj   +1 more source

Sudden Cardiac Death in Athletes: Magnitude, Causes, and Prevention Strategies - A Literature Review

Quality in Sport
Sudden cardiac death (SCD) in athletes, though rare, is the leading cause of exercise-related mortality and poses significant concern due to the symbolic health and vitality of athletes.
Bohdan Melnyk, Artur Rygielski, Emilia Latour, Marianna Latour, Roksana Judek, Mariia Melnyk   +5 more
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The Many Faces of Arrhythmogenic Cardiomyopathy: An Overview

The Application of Clinical Genetics, 2023
Hanna J Tadros,1 Christina Y Miyake,1,2 Debra L Kearney,3 Jeffrey J Kim,1 Susan W Denfield4 1Department of Pediatrics, Section of Pediatric Cardiology, Texas Children’s Hospital, Baylor College of Medicine, Houston, TX, USA; 2Department of Molecular ...
Tadros HJ, Miyake CY, Kearney DL, Kim JJ, Denfield SW   +4 more
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