Wenwen Zhang
No 1#, Minde Road
Nanchang, China
Nanchang, China
Last Updated: 09/26/2026
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Found 12 publications
Digenic Inheritance of PROC and SERPINC1 Mutations Contributes to Multiple Sites Venous Thrombosis.
Journal: Hamostaseologie
Published: January 15, 2024
Endovascular Strategy for Inferior Vena Cava Thrombosis Secondary to Deep Venous Thrombosis of the Lower Extremities: Early Experience From Two Centres.
Journal: Vascular and endovascular surgery
Published: March 30, 2023
The external jugular vein is a feasible and safe alternative access for retrieval of inferior vena cava filter.
Journal: The journal of vascular access
Published: February 16, 2022
A retrospective comparison of thrombectomy followed by stenting and thrombectomy alone for the management of deep vein thrombosis with May-Thurner syndrome.
Journal: Journal of vascular surgery. Venous and lymphatic disorders
Published: May 08, 2020
IL-33 promotes the progression of vascular restenosis after carotid artery balloon injury by promoting carotid artery intimal hyperplasia and inflammatory response.
Journal: Clinical and experimental pharmacology & physiology
Published: March 10, 2020
Drug-eluting stent specifically designed to target vascular smooth muscle cell phenotypic modulation attenuated restenosis through the YAP pathway.
Journal: American journal of physiology. Heart and circulatory physiology
Published: July 13, 2019
Exome sequencing reveals a de novo PRKG1 mutation in a sporadic patient with aortic dissection.
Journal: BMC medical genetics
Published: April 17, 2018
Endovascular Treatment of Ruptured Pancreaticoduodenal Artery Aneurysm with Celiac Axis Stenosis.
Journal: Annals of vascular surgery
Published: April 16, 2018
Familial early-onset deep venous thrombosis associated with a novel HRG mutation.
Journal: European journal of medical genetics
Published: June 12, 2017
Whole exome sequencing reveals a stop-gain mutation of PKD2 in an autosomal dominant polycystic kidney disease family complicated with aortic dissection.
Journal: BMC medical genetics
Published: March 19, 2017
Exome sequencing identified a novel SMAD2 mutation in a Chinese family with early onset aortic aneurysms.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: February 03, 2017
Showing 1-12 of 12
Last Updated: 09/26/2026