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Dao Wu Wang

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Articles 14
Citations 197
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Recent Articles
1.
Zhang B, Wu Y, Zhou C, Xie J, Zhang Y, Yang X, et al.
BMC Med . 2024 Sep; 22(1):361. PMID: 39227800
Background: Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiomyopathy characterized with progressive cardiac fibrosis and heart failure. However, the exact mechanism driving the progression of cardiac fibrosis and heart failure in...
2.
Cai L, Zeng Q, Gao C, Wu W, Shen J, Wu B, et al.
J Assist Reprod Genet . 2022 Nov; 39(11):2483-2504. PMID: 36422765
Purpose: This preclinical study aimed to evaluate whether using transferred mosaic embryos (primarily selected by embryonic morphology assessment (EMA) and compared by the noninvasive preimplantation genetic testing for aneuploidy (niPGT-A)...
3.
Wang L, Liu H, Zhu C, Gu K, Yang G, Chen H, et al.
BMC Cardiovasc Disord . 2021 Sep; 21(1):425. PMID: 34496747
Background: Accelerated idioventricular rhythm (AIVR) is often transient, considered benign and requires no treatment. This observational study aims to investigate the clinical manifestations, treatment, and prognosis of frequent AIVR. Methods:...
4.
Stiles M, Wilde A, Abrams D, Ackerman M, Albert C, Behr E, et al.
J Arrhythm . 2021 Jun; 37(3):481-534. PMID: 34141003
This international multidisciplinary document intends to provide clinicians with evidence-based practical patient-centered recommendations for evaluating patients and decedents with (aborted) sudden cardiac arrest and their families. The document includes a...
5.
Stiles M, Wilde A, Abrams D, Ackerman M, Albert C, Behr E, et al.
Heart Rhythm . 2020 Oct; 18(1):e1-e50. PMID: 33091602
This international multidisciplinary document intends to provide clinicians with evidence-based practical patient-centered recommendations for evaluating patients and decedents with (aborted) sudden cardiac arrest and their families. The document includes a...
6.
Li X, Li Z, Wang D, Wang D, Wang Y
Cardiology . 2020 Aug; 145(10):623-632. PMID: 32818936
Brugada syndrome (BrS) is a known cause of sudden cardiac death (SCD) characterized by abnormal electrocardiograms and fatal arrhythmias. The variants in KCND3 encoding the KV4.3 potassium-channel (the α-subunit of...
7.
Ding Y, Yang J, Chen P, Lu T, Jiao K, Tester D, et al.
J Am Heart Assoc . 2020 Aug; 9(17):e017055. PMID: 32808564
Background (sorbin and SH3 domain-containing 2b) was recently identified as a cardiomyopathy gene from a zebrafish mutagenesis screen. However, cardiac functions of its mammalian ortholog remain elusive. Methods and Results...
8.
Li X, Li Z, Chen P, Wang Y, Wang D, Wang D
BMC Med Genet . 2020 Jul; 21(1):144. PMID: 32631253
Background: Autosomal dominant hypertension with brachydactyly type E syndrome caused by pathogenic variants in the PDE3A gene was first reported in 2015. To date, there are only a few reports...
9.
Li Z, Chen P, Li C, Tan L, Xu J, Wang H, et al.
Heart Rhythm . 2019 Sep; 17(2):305-312. PMID: 31521807
Background: Sudden cardiac death due to malignant arrhythmias is a common cause of death in dilated cardiomyopathy (DCM). Whether genetic variants increase the risk of arrhythmias in DCM is unknown....
10.
Li Z, Chen P, Xu J, Yu B, Li X, Wang D, et al.
Int J Cardiol . 2019 Jan; 279:122-125. PMID: 30638982
Background: Pathogenic variants in human phospholamban coding gene (PLN) are known to cause hereditary dilated cardiomyopathy with heart failure in an autosomal dominant mode. Methods: We performed high-depth targeted next-generation...