Results 61 to 70 of about 7,984 (209)

Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis. [PDF]

, 2019
[No ...
Anastastakis, Aris,, Asimaki, Angeliki,, Basso, Cristina,, Bauce, Barbara,, Brunckhorst, Corinna,, Bucciarelli-Ducci, Chiara, Calkins, Hugh,, Corrado, Domenico,, Duru, Firat,, Elliott, Perry,, Hamilton, Robert M.,, Hauer, Richard N.W.,, Haugaa, Kristina H.,, James, Cynthia A.,, Judge, Daniel,, Link, Mark S.,, Lund University., Lund University., Marchlinski, Francis E.,, Marcus, Frank I.,, Marra, Martina Perazzolo,, Mazzanti, Andrea,, McKenna, William J.,, Mestroni, Luisa,, Pantazis, Antonis,, Pelliccia, Antonio, Pilichou, Kalliopi,, Platonov, Pyotr G.A.,, Protonotarios, Alexandros,, Rampazzo, Alessandra,, Saffitz, Jeffry E.,, Saguner, Ardan M.,, Schmied, Christian,, Sharma, Sanjay,, Tandri, Hari,, Te Riele, Anneline S.J.M.,, Thiene, Gaetano,, Tsatsopoulou, Adalena, Van Tintelen, Peter J.,, Wichter, Thomas, Zareba, Wojciech,, Zorzi, Alessandro,   +41 more
core   +4 more sources

Genome Sequencing Uncovers Additional Findings in Phelan‐McDermid Syndrome

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 198, Issue 7, Page 126-134, October 2025.
ABSTRACT Phelan‐McDermid syndrome (PMS) is a genetic condition caused by deletions of chromosome 22q13.3 or pathogenic variants in the SHANK3 gene. Neurologic features typically include intellectual disability, autism spectrum disorder, hypotonia, and absent speech, though there is considerable variability even among individuals with the same molecular
Rachel Gore Moses, Morgan Similuk, Alexandra Hehn, Rylee Duncan, Margaret Pekar, Eliza Gordon‐Lipkin, Maria T. Acosta, Deena Zeltser, Nadjalisse Reynolds‐Lallement, Latha Soorya, Mustafa Sahin, Tess Levy, Alexander Kolevzon, Joseph D. Buxbaum, Elizabeth Berry‐Kravis, Craig M. Powell, Jonathan A. Bernstein, Mari Tokita, Bryce A. Seifert, Rajarshi Ghosh, Magdalena A. Walkiewicz, Audrey Thurm   +21 more
wiley   +1 more source

The multi-modality cardiac imaging approach to the Athlete's heart: an expert consensus of the European Association of Cardiovascular Imaging [PDF]

, 2015
The term 'athlete's heart' refers to a clinical picture characterized by a slow heart rate and enlargement of the heart. A multi-modality imaging approach to the athlete's heart aims to differentiate physiological changes due to intensive training in the
Abergel, Abhayaratna, Andersson, Angell, Bartram, Basavarajaiah, Blair, Bossone, Bruder, Caso, Chandra, Corrado, Corrado, D'Andrea, D'Andrea, D'Andrea, D'Andrea, D'Andrea, D'Andrea, D'Andrea, Di Paolo, Douglas, Estorch, Fagard, Fagard, Florescu, Gabrielli, Galderisi, Galderisi, Garber, George, Gilbert, Goldhammer, Grothues, Hauser, Hildick-Smith, Kalliokoski, Kim, Knutsen, La Gerche, La Gerche, Ljungqvist, Mahrholdt, Makan, Maron, Maron, Maron, Maron, Maron, Matsumura, Matsuo, Montgomery, Moon, Moon, Morganroth, Mousavi, Nagueh, Nottin, O'Hanlon, Pattynama, Payne, Pelliccia, Pelliccia, Petersen, Pluim, Prakken, Rehr, Richand, Rickers, Rudski, Saghir, Scharf, Scharhag, Schwartz, Semelka, Sen-Chowdhry, Sen-Chowdhry, Severino, Sharma, Shave, Shave, Spirito, Steinvil, Teramoto, Terry, Thomas, Urhausen, Vinereanu, Whyte, Wolfe, Zeppilli, Zoncu   +91 more
core   +4 more sources

Arrhythmogenic Right Ventricular Cardiomyopathy and Cor Triatriatum Dexter: An Unreported Association

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT We present a 74‐year‐old patient with a previous diagnosis of arrhythmogenic right ventricular cardiomyopathy manifesting as heart failure where a concomitant cor triatriatum dexter has accidentally been diagnosed by echocardiography. The association between arrhythmogenic right ventricular cardiomyopathy and cor triatriatum dexter has not ...
Erica Franco, Chiara Rovera, Claudio Moretti, Pier Paolo Bassareo   +3 more
wiley   +1 more source

Role of Catheter Ablation in Arrhythmogenic Right Ventricular Dysplasia

Indian Pacing and Electrophysiology Journal, 2005
Arrhythmogenic right ventricular dysplasia/cardiomyopathy is a disorder characterized by frequent ventricular tachycardia originating from the right ventricle and fibro-fatty replacement of right ventricular myocardium. Though the disorder was originally
Guy Fontaine, Johnson Francis
doaj  

Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: Mechanisms and Management

Research Reports in Clinical Cardiology, 2020
Ahmed AlTurki,1 Bader Alotaibi,1 Jacqueline Joza,1 Riccardo Proietti2 1Division of Cardiology, McGill University Health Center, Montreal, QC, Canada; 2Department of Cardiac, Thoracic, Vascular Sciences, and Public Health, University of Padua, Padua ...
AlTurki A, Alotaibi B, Joza J, Proietti R   +3 more
doaj  

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
core   +2 more sources

Comparing Two‐Dimensional Ellipsoid Model Variants in Estimating Three‐Dimensional Echocardiographic Right Ventricular Volume in Dogs

Journal of Veterinary Internal Medicine, Volume 39, Issue 5, September/October 2025.
ABSTRACT Background Determining right ventricular (RV) volume typically requires three‐dimensional imaging due to its complex shape. The ellipsoid model offers a two‐dimensional alternative, employing area‐ or linear‐based formulas with further variations depending on the echocardiographic views used for measurements.
Robert Ciardullo, Brittany E. Tagg, Elisabeth Nesta, Shana B. Mintz, Romain Pariaut, Weihow Hsue   +5 more
wiley   +1 more source

Arrhythmogenic right ventricular dysplasia: A case report

CorSalud, 2015
Arrhythmogenic right ventricular dysplasia is a heart muscle disease that predominantly affects the right ventricle, bringing about the replacement of normal myocardium with fatty or fibrofatty tissue and causing sudden death in young individuals ...
Tessa Negrín Valdés, Livian M. Lage López, Guillermo R. Quintana Cañizares, Alexander Santos Pérez, Amarilys Valero Hernández   +4 more
doaj  

Right atrial remodelling and prognosis in patients with severe atrial functional tricuspid regurgitation

ESC Heart Failure, Volume 12, Issue 4, Page 2909-2920, August 2025.
Abstract Aims Atrial functional tricuspid regurgitation (AFTR) is increasingly recognized as a distinct cause of tricuspid regurgitation, yet data on outcomes and their determinants are limited. This study examines the prognostic role of right atrial (RA) remodelling in patients with severe AFTR.
Soongu Kwak, Dong‐Jae Han, Seung‐Pyo Lee, Ho Young Hwang, Hyung‐Kwan Kim, Yong‐Jin Kim, Kyung Hwan Kim, Jae Woong Choi, Jun‐Bean Park   +8 more
wiley   +1 more source