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Keyword Connections - dilated cardiomyopathy Keywords

Connection Type	Connection
Journals	Scientific reports The Analyst journal of clinical medicine international journal of cardiology heart & vasculature clinical and applied thrombosis/hemostasis : official journal of the international academy of clinical and applied thrombosis/hemostasis cell research jacc clinical electrophysiology journal of cardiac failure laboratory investigation; a journal of technical methods and pathology journal of the formosan medical association = taiwan yi zhi the international journal of cardiovascular imaging journal of molecular and cellular cardiology surgical technology international the canadian journal of cardiology journal of cardiovascular and thoracic research basic research in cardiology echocardiography (mount kisco, ny)
Research Groups	No Research Group Connected
Bibliographies	[1] Native T1 time and extracellular volume fraction in differentiation of normal myocardium from non-ischemic dilated and hypertrophic cardiomyopathy myocardium: A systematic review and meta-analysis. [2] Latest Advances in Annuloplasty Protheses for Valvular Reconstructive Surgery. [3] Left Atrial Function Using Cardiovascular Magnetic Resonance Imaging Independently Predicts Life-Threatening Arrhythmias in Patients Referred to Receive a Primary Prevention Implantable Cardioverter Defibrillator. [4] Metabolic reprogramming orchestrates CD4 T-cell immunological status and restores cardiac dysfunction in autoimmune induced-dilated cardiomyopathy mice. [5] The circulating level of interleukins 6 and 18 in ischemic and idiopathic dilated cardiomyopathy. [6] Decreased eGFR Is Associated With Ischemic Stroke in Patients With Dilated Cardiomyopathy. [7] NDUFAB1 confers cardio-protection by enhancing mitochondrial bioenergetics through coordination of respiratory complex and supercomplex assembly. [8] Metabolic Profiling Associates with Disease Severity in Non-Ischemic Dilated Cardiomyopathy. [9] Myocardial work is a predictor of exercise tolerance in patients with dilated cardiomyopathy and left ventricular dyssynchrony. [10] Sex Differences in the Long-term Prognosis of Dilated Cardiomyopathy. [11] Heart non-specific effector CD4 T cells protect from postinflammatory fibrosis and cardiac dysfunction in experimental autoimmune myocarditis. [12] Laundry wastewater treatment using a combination of sand filter, bio-char and teff straw media. [13] Viral expression of a SERCA2a-activating PLB mutant improves calcium cycling and synchronicity in dilated cardiomyopathic hiPSC-CMs. [14] Engineering anisotropic cardiac monolayers on microelectrode arrays for non-invasive analyses of electrophysiological properties. [15] Echocardiographic parameters, speckle tracking, and brain natriuretic peptide levels as indicators of progression of indeterminate stage to Chagas Cardiomyopathy. [16] Dysregulation of Calcium Handling in Duchenne Muscular Dystrophy-Associated Dilated Cardiomyopathy: Mechanisms and Experimental Therapeutic Strategies. [17] Pigs with δ-sarcoglycan deficiency exhibit traits of genetic cardiomyopathy. [18] Modifications of Titin Contribute to the Progression of Cardiomyopathy and Represent a Therapeutic Target for Treatment of Heart Failure [19] 2q37 deletion syndrome confirmed by high-resolution cytogenetic analysis [20] characteristics of syncope in patients with dilated cardiomyopathy [21] polychemotherapy induced cardiomyopathy in patient with breast cancer [22] elevated serum bisphenol a level in patients with dilated cardiomyopathy [23] voluntary exercise improves cardiac function and prevents cardiac remodeling in a mouse model of dilated cardiomyopathy [24] breast cancer clinical trial of chemotherapy and trastuzumab: potential tool to identify cardiac modifying variants of dilated cardiomyopathy [25] miocardiopatia terminal com insuficiência mitral secundária: tratamento com implante de prótese e remodelamento interno do ventrículo esquerdo end stage cardiomyopathy and secondary mitral insufficiency: surgical alternative with prostesis implant and left ventricular remodelling [26] novel linkage of lmna single nucleotide polymorphism with dilated cardiomyopathy in an indian case study [27] etiology-specific assessment of predictors of long-term survival in chronic systolic heart failure [28] hypocalcemic cardiomyopathy presenting as cardiogenic shock [29] Effects of candesartan on electrical remodeling in the hearts of inherited dilated cardiomyopathy model mice. [30] The Role of Cardiac MRI in the Management of Ventricular Arrhythmias in Ischaemic and Non-ischaemic Dilated Cardiomyopathy. [31] The effectiveness of cardiac rehabilitation in non-ischemic dilated cardiomyopathy patients: A pilot study. [32] Importance of Genetic Testing in Dilated Cardiomyopathy: Applications and Challenges in Clinical Practice. [33] Thyroid Storm-induced Severe Dilated Cardiomyopathy and Ventricular Tachycardia. [34] Dilated cardiomyopathy as a rare presentation of the pulmonary sequestration: A case report with aberrant vessel from aorta to left lower pulmonary lobe. [35] Metabolic reprogramming orchestrates CD4 T-cell immunological status and restores cardiac dysfunction in autoimmune induced-dilated cardiomyopathy mice. [36] The circulating level of interleukins 6 and 18 in ischemic and idiopathic dilated cardiomyopathy. [37] Decreased eGFR Is Associated With Ischemic Stroke in Patients With Dilated Cardiomyopathy. [38] Increased mortality and ICD therapies in ischemic versus non-ischemic dilated cardiomyopathy patients with cardiac resynchronization having survived until first device replacement. [39] Association between right ventricular two-dimensional strain and exercise capacity in patients with either idiopathic or ischemic dilated cardiomyopathy [40] Metabolic Profiling Associates with Disease Severity in Non-Ischemic Dilated Cardiomyopathy. [41] Myocardial work is a predictor of exercise tolerance in patients with dilated cardiomyopathy and left ventricular dyssynchrony. [42] Sex Differences in the Long-term Prognosis of Dilated Cardiomyopathy. [43] Dysregulation of Calcium Handling in Duchenne Muscular Dystrophy-Associated Dilated Cardiomyopathy: Mechanisms and Experimental Therapeutic Strategies. [44] The altered expression of autophagy-related genes participates in heart failure: NRBP2 and CALCOCO2 are associated with left ventricular dysfunction parameters in human dilated cardiomyopathy. [45] Myocardium of patients with dilated cardiomyopathy presents altered expression of genes involved in thyroid hormone biosynthesis. [46] Left Ventricular Geometry and Replacement Fibrosis Detected by cMRI Are Associated with Major Adverse Cardiovascular Events in Nonischemic Dilated Cardiomyopathy [47] characteristics of syncope in patients with dilated cardiomyopathy [48] mutation in δ-sg gene in familial dilated cardiomyopathy [49] the correlation of pparα activity and cardiomyocyte metabolism and structure in idiopathic dilated cardiomyopathy during heart failure progression [50] elevated serum bisphenol a level in patients with dilated cardiomyopathy [51] inter- not intraindividual differences in stweak levels predict functional deterioration and mortality in patients with dilated cardiomyopathy [52] sevoflurane in an infant with dilated cardiomyopathy due to myocarditis and hypocalcaemia [53] voluntary exercise improves cardiac function and prevents cardiac remodeling in a mouse model of dilated cardiomyopathy [54] a young man with hemoptysis: rare association of idiopathic pulmonary hemosiderosis, celiac disease and dilated cardiomyopathy [55] breast cancer clinical trial of chemotherapy and trastuzumab: potential tool to identify cardiac modifying variants of dilated cardiomyopathy [56] a1180v of cardiac sodium channel gene (scn5a): is it a risk factor for dilated cardiomyopathy or just a common variant in han chinese? [57] resident progenitor cardiac cells in patients with dilated cardiomyopathy and congestive heart failure [58] novel linkage of lmna single nucleotide polymorphism with dilated cardiomyopathy in an indian case study [59] arrhythmic risk and genetic variations in dilated cardiomyopathy patients [60] Understanding the genetics of adult-onset dilated cardiomyopathy: what a clinician needs to know