Results 71 to 80 of about 296,757 (381)
Recommendations for participation in competitive and leisure time sport in athletes with cardiomyopathies, myocarditis, and pericarditis: position statement of the Sport Cardiology Section of the European Association of Preventive Cardiology (EAPC).
European Heart Journal, 2018 Myocardial diseases are associated with an increased risk of potentially fatal cardiac arrhythmias and sudden cardiac death/cardiac arrest during exercise, including hypertrophic cardiomyopathy, dilated cardiomyopathy, left ventricular non-compaction ...A. Pelliccia, E. Solberg, M. Papadakis, P. Adami, A. Biffi, S. Caselli, A. La Gerche, J. Niebauer, A. Pressler, C. Schmied, L. Serratosa, M. Halle, F. van Buuren, M. Borjesson, F. Carré, N. Panhuyzen-Goedkoop, H. Heidbuchel, I. Olivotto, D. Corrado, G. Sinagra, Sanjay Sharma +20 moresemanticscholar +1 more sourceDilated cardiomyopathy [PDF]
Nature Reviews Disease Primers, 2019 Dilated cardiomyopathy (DCM) is a clinical diagnosis characterized by left ventricular or biventricular dilation and impaired contraction that is not explained by abnormal loading conditions (for example, hypertension and valvular heart disease) or coronary artery disease.Schultheiss H. -P., Fairweather D. L., Caforio A. L. P., Escher F., Hershberger R. E., Lipshultz S. E., Liu P. P., Matsumori A., MAZZANTI, ANDREA, McMurray J., Priori S. G. +10 moreopenaire +5 more sourcesDilated cardiomyopathies and non-compaction cardiomyopathy [PDF]
Herz, 2020 AbstractDilated cardiomyopathy (DCM) is the most common form of cardiomyopathy and one of the most common causes of heart failure. It is characterized by left or biventricular dilation and a reduced systolic function. The causes are manifold and range from myocarditis to alcohol and other toxins, to rheumatological, endocrinological, and metabolic ...Anja Hänselmann, Dominik Berliner, Johann Bauersachs, Christian Veltmann +3 moreopenaire +3 more sourcesInternational criteria for electrocardiographic interpretation in athletes: Consensus statement. [PDF]
, 2017 Sudden cardiac death (SCD) is the leading cause of mortality in athletes during sport. A variety of mostly hereditary, structural or electrical cardiac disorders are associated with SCD in young athletes, the majority of which can be identified or ...Aagaard, Aaron Baggish, Ackerman, Anderson, Andre La Gerche, Antonio Pelliccia, Antzelevitch, Aro, Asif, Baggish, Bakken, Basavarajaiah, Bayés de Luna, Bazett, Behr, Bent, Bent, Bessem, Biffi, Biffi, Bjørnstad, Borjesson, Brosnan, Brosnan, Brosnan, Brosnan, Calore, Calore, Calò, Carmen Adamuz, Chad A Asplund, Chandra, Chen, Chou, Christian M Schmied, Chung, Chung, Cohen, Corrado, Corrado, Corrado, Corrado, Corrado, Daubert, David M Shipon, David S Owens, Daviglus, Delise, Delise, Desai, Dhutia, Di Paolo, Domenico Corrado, Drezner, Drezner, Drezner, Drezner, Drezner, Drezner, Drezner, Dunn, Eckart, Elliott, Eugene H Chung, Exeter, Finocchiaro, Fudge, Gati, Goldenberg, Gollob, Gordon Cohen, Groh, Haghjoo, Hancock, Hank F Pelto, Harmon, Harmon, Haïssaguerre, Heidbuchel, Heidbüchel, Hein Heidbuchel, Hill, Huston, Irfan M Asif, Jack C Salerno, James, Johnson, Johnson, Jonathan A Drezner, Jordan M Prutkin, Josef Niebauer, Joseph C Marek, Junttila, Kapplinger, Kim, Kim, Kimberly G Harmon, Klein, Klein, La Gerche, Lakdawala, Le, Link, MacAlpin, Macfarlane, Magalski, Magee, Malfatto, Malhotra, Marco V Perez, Marcus, Marek, Maron, Maron, Maron, Maron, Maron, Maron, Mason, Mathew G Wilson, Mats Borjesson, Meyer, Meytes, Michael J Ackerman, Michael Papadakis, Michael S Emery, Migliore, Nasir, Nathan R Riding, Northcote, Noseworthy, Noseworthy, Novak, Papadakis, Papadakis, Pelliccia, Pelliccia, Pelliccia, Pickham, Platonov, Postema, Price, Prior, Priori, Quattrini, Ranthe, Ranthe, Rautaharju, Rawlins, Ricardo Stein, Riding, Riding, Rose, Rosso, Rowin, Ruwald, Ryan, Saguner, Sahlén, Sanjay Sharma, Sathanandam, Sawant, Schnell, Schwartz, Schwartz, Schwartz, Sharma, Sheikh, Sheikh, Sheikh, Silvana Molossi, Sohaib, Stein, Surawicz, Taggart, Takken, Tan, Tess Saarel, Tester, Tester, Tester, Tikkanen, Tikkanen, Uberoi, Uberoi, Uhm, Verdile, Victor F Froelicher, Victoria L Vetter, Vincent, Viskin, Wasfy, Weiner, Wilde, Williams, Wilson, Xiao, Zaidi, Zorzi +198 morecore +2 more sourcesAdaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel
Genetics in Medicine, 2018 PurposeIntegrating genomic sequencing in clinical care requires standardization of variant interpretation practices. The Clinical Genome Resource has established expert panels to adapt the American College of Medical Genetics and Genomics/Association for M. Kelly, C. Caleshu, A. Morales, J. Buchan, Zena T. Wolf, S. Harrison, S. Cook, Mitchell W Dillon, John Garcia, Eden V. Haverfield, J. Jongbloed, D. Macaya, A. Manrai, Kate M. Orland, G. Richard, Katherine G Spoonamore, Matthew Thomas, K. Thomson, L. Vincent, R. Walsh, H. Watkins, N. Whiffin, J. Ingles, J. P. van Tintelen, C. Semsarian, J. Ware, R. Hershberger, B. Funke +27 moresemanticscholar +1 more sourceCompound Heterozygous MRPS14 Variants Associated With Leigh Syndrome
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT
MRPS14 (uS14m) is a nuclear‐encoded ribosomal protein important for mitochondria‐specific translation. To date, only a single individual with a recessive MRPS14‐related disorder (also known as COXPD38) has been reported. We report an additional subject possessing novel compound heterozygous MRPS14 variants (p.Asp37Asn, p.Asn60Asp). The subject Maria Gabriela Otero, Christina Freeman, Ruchi Shah, Renkui Bai, Hong Cui, Marian Castro, Zachary Myers, Eric Choy, Derek Chan, Molly Easter, Sophia Y. Zhao, Madeline Babros, Ruchi Garg, Matthew Deardorff, Franklin Moser, Tyler Mark Pierson +15 morewiley +1 more sourceEvolving trends in epidemiology and natural history of cardiac amyloidosis: 30-year experience from a tertiary referral center for cardiomyopathies
Frontiers in Cardiovascular Medicine, 2022 ObjectiveNatural history of cardiac amyloidosis (CA) is poorly understood. We aimed to examine the changing mortality of different types of CA over a 30-year period.Patients and methodsConsecutive patients included in the “Trieste CA Registry” from ...Aldostefano Porcari, Valentina Allegro, Riccardo Saro, Guerino Giuseppe Varrà, Linda Pagura, Maddalena Rossi, Andrea Lalario, Francesca Longo, Renata Korcova, Matteo Dal Ferro, Andrea Perkan, Franca Dore, Rossana Bussani, Giovanni Maria De Sabbata, Francesco Zaja, Francesco Zaja, Marco Merlo, Gianfranco Sinagra +17 moredoaj +1 more sourceAssessment of biventricular function by three-dimensional speckle tracking echocardiography in adolescents and young adults with human immunodeficiency virus infection. a pilot study. [PDF]
, 2019 Background. The purpose of the study was to assess biventricular parameters of wall deformation with three-dimensional speckle tracking echocardiography (3DSTE) in adolescents and young adults with human immunodeficiency virus infection (HIV) on ...Ajassa, Camilla, Capotosto, Lidia, Cavallari, EUGENIO NELSON, D'Ettorre, Gabriella, Gaudio, Carlo, Lucchetti, Pietro, Mangieri, Enrico, Placanica, Giuseppe, Ricci, Serafino, Rosaria Ciardi, Maria, Tanzilli, Gaetano, Vitarelli, Antonino, Vullo, Vincenzo +12 morecore +1 more sourceEHRA/HRS/APHRS/SOLAECE expert consensus on atrial cardiomyopathies: definition, characterization, and clinical implication.
Europace, 2016 The atria provide an important contribution to cardiac function.1,2 Besides their impact on ventricular filling, they serve as a volume reservoir, host pacemaker cells and important parts of the cardiac conduction system (e.g.A. Goette, J. Kalman, L. Aguinaga, J. Akar, J. Cabrera, Shih‐Ann Chen, S. Chugh, D. Corradi, A. d'Avila, D. Dobrev, G. Fenelon, M. Gonzalez, S. Hatem, Robert H. Helm, G. Hindricks, S. Ho, B. Hoit, J. Jalife, Young-Hoon Kim, G. Lip, Changsheng Ma, G. Marcus, K. Murray, A. Nogami, P. Sanders, W. Uribe, D. V. Van Wagoner, S. Nattel +27 moresemanticscholar +1 more source
