Results 31 to 40 of about 145,753 (323)

Peripartum cardiomyopathy: diagnosis and management [PDF]

, 2017
No abstract ...
Coats, Caroline J., Dalzell, Jonathan R., Jackson, Alice M., Jhund, Pardeep S., Petrie, Mark C., Walker, Niki L.   +5 more
core   +1 more source

Assessment 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 more
core   +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

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

Hereditary dilated cardiomyopathy

Clinical Cardiology, 1995
AbstractDilated cardiomyopathy (DCM) is a common and important cause of morbidity and mortality. Many factors can contribute to the development of this disorder, although most commonly the etiology is unexplained. However, recent studies in individuals with idiopathic DCM now reveal a heritable cause in 20–30% of individuals.
T R, McMinn, J, Ross
openaire   +2 more sources

Integrated analysis reveals the dysfunction of intercellular communication and metabolic signals in dilated cardiomyopathy

Heliyon
Aims: Dilated cardiomyopathy refers to a heart muscle condition characterized by structural and functional irregularities in the myocardium that are not related to ischemia. Due to diverse etiologies such as genetic mutations, infections, and exposure to
Rui Shi, Xiue Ma, Mi Zhou, Xin Xie, Liang Xu   +4 more
doaj   +1 more source

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

Similar burden of rare genetic variants in ischemic and non-ischemic dilated cardiomyopathy

Frontiers in Cardiovascular Medicine
BackgroundThe aim of the study was to determine the prevalence of rare disease-causing variants in cardiomyopathy-associated genes in a cohort of patients with ischemic and non-ischemic dilated cardiomyopathy undergoing heart transplant.MethodsWe ...
Louie Cao, Joshua Rushakoff, Ian Williamson, Anja Karlstaedt, Michelle Kittleson, Lawrence Czer, Evan P. Kransdorf   +6 more
doaj   +1 more source

Molecular analysis of sarcomeric and non-sarcomeric genes in patients with hypertrophic cardiomyopathy. [PDF]

, 2015
Background: Hypertrophic cardiomyopathy (HCM) is a common genetic heart disorder characterized by unexplained left ventricle hypertrophy associated with non-dilated ventricular chambers.
BOTTILLO, IRENE, CAPUTO, VIVIANA, Castori, M, D'ANGELANTONIO, DANIELA, De Bernardo, C, Giannarelli, D, GRAMMATICO, Paola, LIPARI, MARTINA, Majore, S, PAIARDINI, ALESSANDRO, PIZZUTI, Antonio, Re, F, Zachara, E   +12 more
core   +1 more source