Results 21 to 30 of about 517,435 (235)

Dilated cardiomyopathy and aldosteronoma: a causal link?

ESC Heart Failure, 2020
The aim of this study is to reveal the causal relationship between dilated cardiomyopathy and aldosteronoma. A 44‐year‐old male dilated cardiomyopathy patient with aldosteronoma, who demonstrated a worse cardiac function after 1 year therapy with ...
Jiyu Zhang, Jin Yang, Yueliang Li
doaj   +1 more source

Prognostic Value of Late Gadolinium Enhancement for the Prediction of Cardiovascular Outcomes in Dilated Cardiomyopathy

Circulation Cardiovascular Imaging, 2020
Supplemental Digital Content is available in the text. Background: Dilated cardiomyopathy is associated with increased risk of major cardiovascular events.
A. Alba, J. Gaztanaga, F. Foroutan, P. Thavendiranathan, M. Merlo, David Alonso-Rodríguez, Víctor Vallejo-García, R. Vidal-Pérez, C. Corros-Vicente, M. Barreiro-Pérez, P. Pazos-López, E. Pérez-David, S. Dykstra, J. Flewitt, J. Pérez-Rivera, María Vázquez-Caamaño, S. Katz, G. Sinagra, L. Køber, J. Poole, H. Ross, M. Farkouh, James A. White   +22 more
semanticscholar   +1 more source

Collagen content, but not the ratios of collagen type III/I mRNAs, differs among hypertensive, alcoholic, and idiopathic dilated cardiomyopathy

Brazilian Journal of Medical and Biological Research, 2008
Cardiac interstitial fibrosis may contribute to ventricular dysfunction and the prognosis of patients with dilated cardiomyopathy. The objective of the present study was to determine if total myocardial collagen content and collagen type III/I (III/I ...
H.N. Soufen, V.M.C. Salemi, I.M.S. Aneas, F.J.A. Ramires, A.M.D. Benício, L.A. Benvenuti, J.E. Krieger, C. Mady   +7 more
doaj   +1 more source

Implications of Genetic Testing in Dilated Cardiomyopathy

Circulation Genomic and Precision Medicine, 2020
Supplemental Digital Content is available in the text. Background: Genetic analysis is a first-tier test in dilated cardiomyopathy (DCM). Electrical phenotypes are common in genetic DCM, but their exact contribution to the clinical course and outcome is ...
J. Verdonschot, M. Hazebroek, I. Krapels, M. Henkens, A. Raafs, Ping Wang, J. Merken, G. Claes, E. Vanhoutte, A. van den Wijngaard, S. Heymans, H. Brunner   +11 more
semanticscholar   +1 more source

Anaesthetic Management of a Patient with Dilated Cardiomyopathy for Fracture Femur Surgery-A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2014
Dilated cardiomyopathy (DCM) is defined as impairment of the ventricular function of the myocardium. The management of a patient with dilated cardiomyopathy, who undergoes a non-cardiac surgery, is always a challenge for an anaesthesiologist, as this ...
Koramutla Pradeep Kumar, Gudaru Jagadesh
doaj   +1 more source

Dysregulation of Calcium Handling in Duchenne Muscular Dystrophy-Associated Dilated Cardiomyopathy: Mechanisms and Experimental Therapeutic Strategies

Journal of Clinical Medicine, 2020
Duchenne muscular dystrophy (DMD) is an X-linked recessive disease resulting in the loss of dystrophin, a key cytoskeletal protein in the dystrophin-glycoprotein complex.
M. Law, Houda Cohen, Ashley A. Martin, A. B. B. Angulski, J. Metzger   +4 more
semanticscholar   +1 more source

Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy

Genome Biology, 2017
Background Genetic variation is an important determinant of RNA transcription and splicing, which in turn contributes to variation in human traits, including cardiovascular diseases. Results Here we report the first in-depth survey of heart transcriptome
Matthias Heinig, Michiel E. Adriaens, Sebastian Schafer, Hanneke W. M. van Deutekom, Elisabeth M. Lodder, James S. Ware, Valentin Schneider, Leanne E. Felkin, Esther E. Creemers, Benjamin Meder, Hugo A. Katus, Frank Rühle, Monika Stoll, François Cambien, Eric Villard, Philippe Charron, Andras Varro, Nanette H. Bishopric, Alfred L. George, Cristobal dos Remedios, Aida Moreno-Moral, Francesco Pesce, Anja Bauerfeind, Franz Rüschendorf, Carola Rintisch, Enrico Petretto, Paul J. Barton, Stuart A. Cook, Yigal M. Pinto, Connie R. Bezzina, Norbert Hubner   +30 more
doaj   +1 more source

Role of Cardiac Magnetic Resonance Imaging in Hypocalcemia-Induced Dilated Cardiomyopathy in Pediatric Population

Indian Journal of Radiology and Imaging, 2021
Background Hypocalcemia is a rare reversible cause of dilated cardiomyopathy in pediatric population. Myocarditis is another more frequent cause of cardiomyopathy with overlapping presenting features.
Ankit Garg, Sushil Azad, Khemendra Kumar, Mona Bhatia, S. Radhakrishnan   +4 more
doaj   +1 more source

Desmoplakin Cardiomyopathy, a Fibrotic and Inflammatory Form of Cardiomyopathy Distinct From Typical Dilated or Arrhythmogenic Right Ventricular Cardiomyopathy

Circulation, 2020
Supplemental Digital Content is available in the text. Background: Mutations in desmoplakin (DSP), the primary force transducer between cardiac desmosomes and intermediate filaments, cause an arrhythmogenic form of cardiomyopathy that has been variably ...
Eric Smith, N. Lakdawala, N. Papoutsidakis, G. Aubert, A. Mazzanti, Anthony C. McCanta, P. Agarwal, P. Arscott, Lisa M. Dellefave‐Castillo, E. Vorovich, K. Nutakki, L. Wilsbacher, S. Priori, D. Jacoby, E. McNally, A. Helms   +15 more
semanticscholar   +1 more source

Psoriasis as risk factor for non-ischemic dilated cardiomyopathy: a population-based cross-sectional study

BMC Cardiovascular Disorders, 2021
Background Psoriasis is a chronic inflammatory skin condition commonly associated with psoriatic arthritis, malignancy, diabetes, inflammatory bowel disease, and cardiovascular disease.
Abbas Alshami, Nasam Alfraji, Steven Douedi, Swapnil Patel, Mohammad Hossain, Deborah Alpert, Dawn Calderon   +6 more
doaj   +1 more source