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2023 ESC Guidelines for the management of cardiomyopathies: Developed by the task force on the management of cardiomyopathies of the European Society of …
• The specific situation of the patient. Unless otherwise provided for by national regulations,
off-label use of medication should be limited to situations where it is in the patient's interest …
off-label use of medication should be limited to situations where it is in the patient's interest …
Role of the CCL2-CCR2 axis in cardiovascular disease: Pathogenesis and clinical implications
H Zhang, K Yang, F Chen, Q Liu, J Ni, W Cao… - Frontiers in …, 2022 - frontiersin.org
The CCL2-CCR2 axis is one of the major chemokine signaling pathways that has received
special attention because of its function in the development and progression of …
special attention because of its function in the development and progression of …
[HTML][HTML] Proposed diagnostic criteria for arrhythmogenic cardiomyopathy: European Task Force consensus report
D Corrado, A Anastasakis, C Basso, B Bauce… - International Journal of …, 2024 - Elsevier
Arrhythmogenic cardiomyopathy (ACM) is a heart muscle disease characterized by
prominent “non-ischemic” myocardial scarring predisposing to ventricular electrical …
prominent “non-ischemic” myocardial scarring predisposing to ventricular electrical …
NFĸB signaling drives myocardial injury via CCR2+ macrophages in a preclinical model of arrhythmogenic cardiomyopathy
Nuclear factor κ-B (NFκB) is activated in iPSC-cardiac myocytes from patients with
arrhythmogenic cardiomyopathy (ACM) under basal conditions, and inhibition of NFκB …
arrhythmogenic cardiomyopathy (ACM) under basal conditions, and inhibition of NFκB …
Fir (e) ing the rhythm: inflammatory cytokines and cardiac arrhythmias
Inflammatory activation is increasingly recognized as a nonconventional risk factor for
arrhythmias, and experimental studies provided robust evidence that this association is …
arrhythmias, and experimental studies provided robust evidence that this association is …
AAV9:PKP2 improves heart function and survival in a Pkp2-deficient mouse model of arrhythmogenic right ventricular cardiomyopathy
Background Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a familial cardiac
disease associated with ventricular arrhythmias and an increased risk of sudden cardiac …
disease associated with ventricular arrhythmias and an increased risk of sudden cardiac …
Frequency, penetrance, and variable expressivity of dilated cardiomyopathy–associated putative pathogenic gene variants in UK biobank participants
Background: There is a paucity of data regarding the phenotype of dilated cardiomyopathy
(DCM) gene variants in the general population. We aimed to determine the frequency and …
(DCM) gene variants in the general population. We aimed to determine the frequency and …
Predicting ventricular tachycardia circuits in patients with arrhythmogenic right ventricular cardiomyopathy using genotype-specific heart digital twins
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetic cardiac disease that
leads to ventricular tachycardia (VT), a life-threatening heart rhythm disorder. Treating ARVC …
leads to ventricular tachycardia (VT), a life-threatening heart rhythm disorder. Treating ARVC …
[HTML][HTML] Myocarditis-like episodes in patients with arrhythmogenic cardiomyopathy: a systematic review on the so-called hot-phase of the disease
Arrhythmogenic cardiomyopathy (ACM) is a genetically determined myocardial disease,
characterized by myocytes necrosis with fibrofatty substitution and ventricular arrhythmias …
characterized by myocytes necrosis with fibrofatty substitution and ventricular arrhythmias …
Susceptibility to innate immune activation in genetically mediated myocarditis
DF Selgrade, DE Fullenkamp, IA Chychula, B Li… - The Journal of Clinical …, 2024 - jci.org
Myocarditis is clinically characterized by chest pain, arrhythmias, and heart failure, and
treatment is often supportive. Mutations in DSP, a gene encoding the desmosomal protein …
treatment is often supportive. Mutations in DSP, a gene encoding the desmosomal protein …