Zhi-an Zhong

Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of the DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy Involving Both Ventricles

Z. Shan, H. Deng, Yubi Lin, 2017, Cardiology.

Clinical and genetic spectrum in Chinese families with Fabry disease: a single‐centre case series

H. Deng, Shulin Wu, X. Fang, 2021, ESC heart failure.

Successful treatment of complex coronary chronic total occlusions improves midterm outcomes.

R. Khouzam, V. Vukcevic, Bin Zhang, 2019, Annals of translational medicine.

Predictors, treatment, and long‐term outcomes of coronary perforation during retrograde percutaneous coronary intervention via epicardial collaterals for recanalization of chronic coronary total occlusion

Bin Zhang, H. Liao, Zhi-an Zhong, 2019, Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions.

Usefulness and Safety of a Novel Modification of the Retrograde Approach for the Long Tortuous Chronic Total Occlusion of Coronary Arteries.

Bin Zhang, Feng Wang, H. Liao, 2017, International heart journal.

Safety and Feasibility of Rotational Atherectomy for Retrograde Recanalization of Chronically Occluded Coronary Arteries

Hongtao Liao, Zhi-an Zhong, Bin Zhang, 2022, Frontiers in Cardiovascular Medicine.

Clinical Prediction Score for Successful Retrograde Procedure in Chronic Total Occlusion Percutaneous Coronary Intervention

Bin Zhang, H. Liao, F. Agyekum, 2016, Cardiology.

Systematic analysis of myocardial immune progression in septic cardiomyopathy: Immune-related mechanisms in septic cardiomyopathy

Zhi-an Zhong, Bin Zhang, Pengyuan Chen, 2023, Frontiers in Cardiovascular Medicine.

Epicardial collateral channel for retrograded recanalization of chronic total occlusion percutaneous coronary intervention: Predictors of failure and procedural outcome

Bin Zhang, H. Liao, Zhi-an Zhong, 2018, Journal of interventional cardiology.

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

Jiana Huang, Weitao Ye, Z. Shan, 2018, BMC Medical Genetics.