Results 31 to 40 of about 591,365 (304)

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

Immunity in dilated cardiomyopathy [PDF]

Heart and Vessels, 1985
Although several immunologic parameters have been found to be abnormal, their precise relationship to the cause of the disease remains unclear. It is believed that a virus initiating a bout of myocarditis may play a role in the perpetuation of the chronic phase, probably via immunologic mediation.
Cassidy, James T., Huber, Sally A., Das, Sunil K.   +2 more
openaire   +3 more sources

Dilated cardiomyopathy in thyrotoxicosis [PDF]

Heart, 1999
Heart failure is a rare manifestation of thyrotoxicosis in patients without heart disease.1-3 We report two cases of thyrotoxicosis and no previous heart disease presenting with severe heart failure. Successful treatment of the thyrotoxicosis resulted in progressive improvement of cardiac function.
S, Goland, S, Shimoni, O, Kracoff
openaire   +2 more sources

Dilated cardiomyopathy as the initial presentation of Becker muscular dystrophy: a systematic review of published cases

Orphanet Journal of Rare Diseases, 2022
There are scarce publications regarding the presentation and outcome of Becker muscular dystrophy in adulthood when idiopathic dilated cardiomyopathy is the initial disease manifestation.
Gaspar Del Rio-Pertuz, Cristina Morataya, Kanak Parmar, Sarah Dubay, Erwin Argueta-Sosa   +4 more
doaj   +1 more source

Cushing’s Disease Presented by Reversible Dilated Cardiomyopathy

Case Reports in Cardiology, 2015
Introduction. Dilated cardiomyopathy is rarely reported among CS patients especially without hypertension and left ventricular hypertrophy. Materials and Methods. We hereby report a Cushing’s syndrome case presenting with dilated cardiomyopathy. Results.
Berna İmge Aydoğan, Demet Menekşe Gerede, Asena Gökçay Canpolat, Murat Faik Erdoğan   +3 more
doaj   +1 more source

Serum Zinc Level in Dilated and Ischemic Cardiomyopathy [PDF]

Journal of Tehran University Heart Center, 2007
Background: Serum trace element alteration has been reported in dilated and ischemic cardiomyopathy. The reports were controversial. We have studied serum Zinc level in cardiomyopathy patients in northern province of Mazandaran and compared them with ...
Ali Ghayemian, Seyed Mahmood Nouraei, Ebrahim Salehifar   +2 more
doaj   +2 more sources

2D Echocardiographic features in low T3 syndrome in chronic heart failure

Asian Journal of Medical Sciences, 2014
Background: Thyroid abnormalities are common in chronic heart failure. Severity of heart failure rises by several fold in patients with thyroid dysfunction.
Arun Kumar
doaj   +1 more source

Genetic Risk of Arrhythmic Phenotypes in Patients with Dilated Cardiomyopathy

Journal of the American College of Cardiology, 2019
Background: Genotype-phenotype correlations in dilated cardiomyopathy (DCM) and in particular the effects of gene variants on clinical outcomes remain poorly understood.
M. Gigli, M. Merlo, S. Graw, G. Barbati, T. Rowland, D. Slavov, D. Stolfo, M. Sweet, M. dal Ferro, Alessandro Altinier, F. Ramani, Francesca Brun, Andrea Cocciolo, Ilaria Puggia, Gaetano Morea, W. McKenna, F. L. La Rosa, Matthew R. G. Taylor, G. Sinagra, L. Mestroni   +19 more
semanticscholar   +1 more source

Lack of Bridge to Recovery in Pediatric Dilated Cardiomyopathy With Left Ventricular Noncompaction

Annals of Thoracic Surgery Short Reports
Background: This study assessed the possibility of a bridge to recovery using the Berlin Heart EXCOR and the histologic characteristics of pediatric patients with dilated cardiomyopathy accompanied by a left ventricular noncompaction phenotype.
Moyu Hasegawa, MD, Masaki Taira, MD, Yuji Tominaga, MD, Takuji Watanabe, MD, Yosuke Kugo, MD, Toshiaki Nagashima, MD, Akima Harada, BS, Takayoshi Ueno, MD, PhD, Shigeru Miyagawa, MD, PhD   +8 more
doaj   +1 more source

Familial Dilated Cardiomyopathy [PDF]

New England Journal of Medicine, 1992
Advances in human genome sequencing have re-invigorated genetics studies of dilated cardiomyopathy (DCM), facilitating genetic testing and clinical applications. With a range of genetic testing options now available, new challenges arise for data interpretation and identifying single pathogenic variants from the many thousands of rare variants present ...
S S, Coughlin, R L, Woosley
openaire   +5 more sources