Results 1 to 10 of about 517,435 (235)

Immune-inflammatory concept of the pathogenesis of chronic heart failure in dogs with dilated cardiomyopathy [PDF]

Veterinary World, 2019
Background: Dilated cardiomyopathy is common in dogs. This form of cardiomyopathy is the main cause of death due to heart disease in dogs. Death can occur suddenly in clinically normal animals as a result of the progression of congestive heart failure ...
Yu Vatnikov, A. Rudenko, P. Rudenko, Ev Kulikov, A. Karamyan, V. Lutsay, I. Medvedev, V. Byakhova, E. Krotova, M. Molvhanova   +9 more
doaj   +2 more sources

Demographic and regional mortality trends in dilated cardiomyopathy in the United States; 1999–2020 [PDF]

SAGE Open Medicine
Background: Dilated cardiomyopathy significantly impacts mortality and hospitalizations in the U.S., yet trends in dilated cardiomyopathy-related mortality are underreported.
Syed Sarmad Javaid, Syed Usama Ashraf, Anoud Khan, Muntaha Irfan, Muhammad Usman Alamgir, Syed Daniyal Ahmed Jilanee, Hamiz Faisal, Muhammad Salman Peryani, Noor Ul Ain, Ismail Khan   +9 more
doaj   +2 more sources

Layer-Specific Strain Analysis in Patients with Dilated Cardiomyopathy [PDF]

Biomedicines
Background/Objectives: This study aimed to evaluate layer-specific strain according to etiology and assess whether subtle changes in longitudinal and circumferential layer strain are involved in predicting cardiac mortality during a two-year follow-up in
Despina-Manuela Toader, Alina Paraschiv, Georgică Târtea, Gabriela Tiucu, Mihai Chițu, Raluca Stănișor, Oana Mirea   +6 more
doaj   +2 more sources

Dilated cardiomyopathy due to novel LMNA mutation: a case report [PDF]

Frontiers in Cardiovascular Medicine
A case of a 44-year-old man presenting with a family history of LMNA mutation and cardiac symptoms (dizziness, weakness, palpitations, and shortness of breath) congruent with dilated cardiomyopathy.
Riddhi Patel, Raj Patel, Ekta Patel, Mehul Patel   +3 more
doaj   +2 more sources

Precise genomic editing of pathogenic mutations in RBM20 rescues dilated cardiomyopathy

Science Translational Medicine, 2022
Mutations in RNA binding motif protein 20 (RBM20) are a common cause of familial dilated cardiomyopathy (DCM). Many RBM20 mutations cluster within an arginine/serine-rich (RS-rich) domain, which mediates nuclear localization. These mutations induce RBM20
Takahiko Nishiyama, Yu Zhang, Miao Cui, Hui Li, E. Sánchez-Ortiz, John R. McAnally, Wei Tan, Jiwoong Kim, Kenian Chen, Lin Xu, R. Bassel-Duby, E. Olson   +11 more
semanticscholar   +1 more source

An Unusual Case of 11αB‐Crystallin (CRYAB) Mutation as a Cause of Dilated Cardiomyopathy With Restrictive Physiology: A Case Report and Focused Review of the Literature [PDF]

Clinical Case Reports
Several diseases have been linked to αB‐crystallin (CRYAB) mutation. However, this mutation is an uncommon cause that has been associated in recent years with the development of dilated cardiomyopathy.
Porras Bueno Cristian Orlando, Cruz Buitrago Roberto Hernando, Mariño Correa Alejandro, Cáceres Méndez Edward Andres, Eugenio Meek, Ríos Dueñas Edgar Giovanni   +5 more
doaj   +2 more sources

A predictive model for canine dilated cardiomyopathy—a meta-analysis of Doberman Pinscher data [PDF]

PeerJ, 2015
Dilated cardiomyopathy is a prevalent and often fatal disease in humans and dogs. Indeed dilated cardiomyopathy is the third most common form of cardiac disease in humans, reported to affect approximately 36 individuals per 100,000 individuals.
Siobhan Simpson, Jennifer Edwards, Richard D. Emes, Malcolm A. Cobb, Nigel P. Mongan, Catrin S. Rutland   +5 more
doaj   +2 more sources

Evidence-Based Assessment of Genes in Dilated Cardiomyopathy

Circulation, 2021
Supplemental Digital Content is available in the text. Background: Each of the cardiomyopathies, classically categorized as hypertrophic cardiomyopathy, dilated cardiomyopathy (DCM), and arrhythmogenic right ventricular cardiomyopathy, has a signature ...
Elizabeth Jordan, Laiken Peterson, Tomohiko Ai, B. Asatryan, L. Bronicki, Emily E. Brown, R. Celeghin, Matthew Edwards, Judy Fan, J. Ingles, C. James, O. Jarinova, Renee Johnson, Daniel P. Judge, N. Lahrouchi, R. L. Lekanne Deprez, R. Lumbers, F. Mazzarotto, A. Medeiros Domingo, Rebecca L. Miller, A. Morales, B. Murray, Stacey Peters, K. Pilichou, Alexandros Protonotarios, C. Semsarian, Palak Shah, P. Syrris, C. Thaxton, J. V. van Tintelen, R. Walsh, Jessica Wang, James S. Ware, R. E. Hershberger   +33 more
semanticscholar   +1 more source

Truncated titin proteins in dilated cardiomyopathy

Science Translational Medicine, 2021
Description Truncating mutations in TTN result in both truncated titin proteins and reduced full-length titin in patient hearts. Tracking titin in dilated cardiomyopathy Truncating variants in TTN, the gene encoding the titin protein, underlie 15 to 25 ...
Q. McAfee, C. Y. Chen, Yifan Yang, M. Caporizzo, M. Morley, A. Babu, Sunhye Jeong, Jeffrey Brandimarto, K. Bedi, Emily Flam, Joseph Cesare, T. Cappola, K. Margulies, B. Prosser, Z. Arany   +14 more
semanticscholar   +1 more source

The combination of carboxy‐terminal propeptide of procollagen type I blood levels and late gadolinium enhancement at cardiac magnetic resonance provides additional prognostic information in idiopathic dilated cardiomyopathy – A multilevel assessment of myocardial fibrosis in dilated cardiomyopathy

European Journal of Heart Failure, 2021
To determine the prognostic value of multilevel assessment of fibrosis in dilated cardiomyopathy (DCM) patients.
A. Raafs, J. Verdonschot, M. Henkens, B. Adriaans, Ping Wang, K. Derks, M. A. Abdul Hamid, C. Knackstedt, V. V. van Empel, J. Díez, H. Brunner-la Rocca, H. Brunner, Arantxa González, S. Bekkers, S. Heymans, M. Hazebroek   +15 more
semanticscholar   +1 more source