Results 21 to 30 of about 296,757 (381)

Heart Failure Subtypes and Cardiomyopathies in Women

Circulation Research, 2022
Heart failure affects over 2.6 million women and 3.4 million men in the United States with known sex differences in epidemiology, management, response to treatment, and outcomes across a wide spectrum of cardiomyopathies that include peripartum ...
E. DeFilippis, A. Beale, T. Martyn, Anubha Agarwal, U. Elkayam, C. Lam, E. Hsich   +6 more
semanticscholar   +1 more source

Lyme Carditis: From Pathophysiology to Clinical Management

Pathogens, 2022
Cardiac involvement is a rare but relevant manifestation of Lyme disease that frequently presents as atrioventricular block (AVB). Immune-mediated injury has been implicated in the pathogenesis of Lyme carditis due to possible cross-reaction between ...
Cinzia Radesich, Eva Del Mestre, Kristen Medo, Giancarlo Vitrella, Paolo Manca, Mario Chiatto, Matteo Castrichini, Gianfranco Sinagra   +7 more
doaj   +1 more source

Sudden cardiac death in young athletes: Literature review of molecular basis [PDF]

, 2020
Intense athletic training and competition can rarely result in sudden cardiac death (SCD). Despite the introduction of pre-participation cardiovascular screening, especially among young competitive athletes, sport-related SCD remains a debated issue ...
Barbara Lombardo, Bruno Mirra, Cristina Mazzaccara, Ferdinando Barretta, Giulia Frisso, Olga Scudiero   +5 more
core   +1 more source

ACVIM consensus statement guidelines for the classification, diagnosis, and management of cardiomyopathies in cats

Journal of Veterinary Internal Medicine, 2020
Cardiomyopathies are a heterogeneous group of myocardial disorders of mostly unknown etiology, and they occur commonly in cats. In some cats, they are well‐tolerated and are associated with normal life expectancy, but in other cats they can result in ...
V. Luis Fuentes, J. Abbott, V. Chetboul, E. Côté, P. Fox, J. Häggström, M. Kittleson, Karsten A Schober, J. Stern   +8 more
semanticscholar   +1 more source

Pediatric Restrictive Cardiomyopathies

Frontiers in Pediatrics, 2022
Restrictive cardiomyopathy (RCM) is the least frequent phenotype among pediatric heart muscle diseases, representing only 2.5–3% of all cardiomyopathies diagnosed during childhood.
R. Ditaranto, A. Caponetti, V. Ferrara, V. Parisi, M. Minnucci, C. Chiti, R. Baldassarre, F. Di Nicola, S. Bonetti, Tammam Hasan, L. Potena, N. Galiè, L. Ragni, E. Biagini   +13 more
semanticscholar   +1 more source

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Nature Genetics, 2020
The heart muscle diseases hypertrophic (HCM) and dilated (DCM) cardiomyopathies are leading causes of sudden death and heart failure in young, otherwise healthy, individuals. We conducted genome-wide association studies and multi-trait analyses in HCM (1,
R. Tadros, C. Francis, Xiao Xu, A. Vermeer, A. Harper, R. Huurman, Ken Kelu Bisabu, R. Walsh, E. T. Hoorntje, W. P. te Rijdt, R. Buchan, Hannah G. van Velzen, M. V. van Slegtenhorst, J. Vermeulen, J. Offerhaus, Wenjia Bai, A. de Marvao, N. Lahrouchi, L. Beekman, J. Karper, J. Veldink, E. Kayvanpour, A. Pantazis, A. Baksi, N. Whiffin, F. Mazzarotto, G. Sloane, Hideaki Suzuki, D. Schneider-Luftman, P. Elliott, P. Richard, F. Ader, E. Villard, P. Lichtner, T. Meitinger, M. Tanck, J. V. van Tintelen, A. Thain, D. Mccarty, R. Hegele, Jason D. Roberts, Julie Amyot, M. Dubé, Julia Cadrin-Tourigny, G. Giraldeau, P. L’allier, P. Garceau, J. Tardif, S. Boekholdt, R. Lumbers, F. Asselbergs, P. Barton, S. Cook, S. Prasad, D. O’Regan, J. van der Velden, K. Verweij, M. Talajic, G. Lettre, Y. Pinto, B. Meder, P. Charron, R. D. de Boer, I. Christiaans, M. Michels, A. Wilde, H. Watkins, P. Matthews, J. Ware, C. Bezzina   +69 more
semanticscholar   +1 more source

Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacement [PDF]

, 2019
Primary mitochondrial dysfunction is an under-appreciated cause of cardiomyopathy, especially when cardiac symptoms are the unique or prevalent manifestation of disease.
Bonnen, Penelope E, Carbo, Miriam, Cerbelli, Bruna, D'Amati, Giulia, Della Monica, Paola Lilla, Falkous, Gavin, Giordano, Carla, Glasgow, Ruth I C, Hardy, Steven A, He, Langping, Morea, Veronica, Perli, Elena, Pignataro, Maria Gemma, Pisano, Annalinda, Re, Federica, Taylor, Robert W, Zacara, Elisabetta   +16 more
core   +2 more sources

miR-21 in Human Cardiomyopathies

Frontiers in Cardiovascular Medicine, 2021
miR-21 is a 22-nucleotide long microRNA that matches target mRNAs in a complementary base pairing fashion and regulates gene expression by repressing or degrading target mRNAs.
Surina Surina, R. A. Fontanella, L. Scisciola, R. Marfella, G. Paolisso, M. Barbieri   +5 more
semanticscholar   +1 more source

Cardiomyopathies

Journal de Radiologie, 2004
Cardiomyopathies include a wide variety of cardiac diseases. The value of MR imaging is not only to provide information about cardiac function, but also to detect the underlying cause of the disease.
J P, Laissy, J N, Dacher, V, Sebban, O, Vignaux   +3 more
openaire   +4 more sources

The Role of Quality Control in Targeted Next-generation Sequencing Library Preparation

Genomics, Proteomics & Bioinformatics, 2016
Next-generation sequencing (NGS) is getting routinely used in the diagnosis of hereditary diseases, such as human cardiomyopathies. Hence, it is of utter importance to secure high quality sequencing data, enabling the identification of disease-relevant ...
Rouven Nietsch, Jan Haas, Alan Lai, Daniel Oehler, Stefan Mester, Karen S. Frese, Farbod Sedaghat-Hamedani, Elham Kayvanpour, Andreas Keller, Benjamin Meder   +9 more
doaj   +1 more source