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1.
SGLT2 inhibitor dapagliflozin attenuates cardiac fibrosis and inflammation by reverting the HIF-2α signaling pathway in arrhythmogenic cardiomyopathy.
FASEB J
; 36(7): e22410, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35713937
2.
Digenic heterozygous mutations of KCNH2 and SCN5A induced young and early-onset long QT syndrome and sinoatrial node dysfunction.
Ann Noninvasive Electrocardiol
; 27(1): e12889, 2022 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34755423
3.
Young and early-onset dilated cardiomyopathy with malignant ventricular arrhythmia and sudden cardiac death induced by the heterozygous LDB3, MYH6, and SYNE1 missense mutations.
Ann Noninvasive Electrocardiol
; 26(4): e12840, 2021 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-33949037
4.
Indicators and prediction models for the severity of Covid-19.
Int J Clin Pract
; 75(10): e14571, 2021 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-34170611
5.
Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population.
Cardiology
; 145(1): 38-45, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-31751991
6.
Compound and heterozygous mutations of KCNQ1 in long QT syndrome with familial history of unexplained sudden death: Identified by analysis of whole exome sequencing and predisposing genes.
Ann Noninvasive Electrocardiol
; 25(1): e12694, 2020 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31565860
7.
Plasma miR-142 predicts major adverse cardiovascular events as an intermediate biomarker of dual antiplatelet therapy.
Acta Pharmacol Sin
; 40(2): 208-215, 2019 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-29891858
8.
Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation.
BMC Med Genet
; 19(1): 148, 2018 08 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-30129429
9.
Compound and heterozygous mutations of DSG2 identified by Whole Exome Sequencing in arrhythmogenic right ventricular cardiomyopathy/dysplasia with ventricular tachycardia.
J Electrocardiol
; 51(5): 837-843, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-30177324
10.
Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death.
J Electrocardiol
; 51(2): 309-315, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29132927
11.
Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of the DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy Involving Both Ventricles.
Cardiology
; 138(1): 41-54, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28578331
12.
Changes of Virtual Planar QRS and T Vectors Derived from Holter in the Populations with and without Diabetes Mellitus.
Ann Noninvasive Electrocardiol
; 21(1): 69-81, 2016 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-25940734
13.
Mechanism of and therapeutic strategy for atrial fibrillation associated with diabetes mellitus.
ScientificWorldJournal
; 2013: 209428, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23576900
14.
Effects of low-level autonomic stimulation on prevention of atrial fibrillation induced by acute electrical remodeling.
ScientificWorldJournal
; 2013: 781084, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23864832
15.
Reactivation of PPARα alleviates myocardial lipid accumulation and cardiac dysfunction by improving fatty acid ß-oxidation in Dsg2-deficient arrhythmogenic cardiomyopathy.
Acta Pharm Sin B
; 13(1): 192-203, 2023 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-36815030
16.
Bacteroides fragilis Supplementation Deteriorated Metabolic Dysfunction, Inflammation, and Aorta Atherosclerosis by Inducing Gut Microbiota Dysbiosis in Animal Model.
Nutrients
; 14(11)2022 May 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-35684000
17.
Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality.
Orphanet J Rare Dis
; 17(1): 183, 2022 05 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35526016
18.
Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel.
Orphanet J Rare Dis
; 17(1): 394, 2022 10 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-36303204
19.
[Efficacy of ibutilide for cardioversion of persistent atrial fibrillation during radiofrequency ablation].
Zhonghua Xin Xue Guan Bing Za Zhi
; 39(11): 1029-32, 2011 Nov.
Artículo
en Zh
| MEDLINE | ID: mdl-22336457
20.
Identification of rare heterozygous linkage R965C-R1309H mutations in the pore-forming region of SCN5A gene associated with complex arrhythmia.
Mol Genet Genomic Med
; 9(5): e1613, 2021 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33764691