Xinchang Liu

发表

Identification of NF1 Frameshift Variants in Two Chinese Families With Neurofibromatosis Type 1 and Early-Onset Hypertension

Xian-liang Zhou, P. Fan, Xueqi Dong, 2021, Frontiers in Pediatrics.

Clinical characteristics and management of coexistent cardiomyopathy in patients with bicuspid aortic valve.

Ya-xin Liu, Y. Qu, Di Zhang, 2023, Journal of geriatric cardiology : JGC.

Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family

Xian-liang Zhou, Ya-xin Liu, P. Fan, 2022, Frontiers in Pediatrics.

Percutaneous Transluminal Renal Angioplasty for Fibromuscular Dysplasia and Prognostic Risk Factors: A Retrospective Chinese Cohort Study

Yankun Yang, Lin Sun, Xin-Chang Liu, 2022, Journal of clinical medicine.

A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension

F. Luo, Ya-xin Liu, P. Fan, 2022, Frontiers in Cardiovascular Medicine.

Identification of a novel frameshift mutation in the SCNN1B causing Liddle syndrome.

Ya-xin Liu, T. Tian, Yu Zhang, 2023, Science bulletin.

A novel missense mutation in obscurin gene in a Chinese consanguineous family with left ventricular noncompaction

Xian-liang Zhou, Ya-xin Liu, Y. Qu, 2022, Journal of geriatric cardiology : JGC.

A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review

Ya-xin Liu, P. Fan, Di Zhang, 2023, Molecular medicine reports.

Extended-spectrum beta-lactamase-producing Klebsiella pneumoniae infection in a neonatal intensive care unit

Guangyong Ye, Rong Lin, Bo Wu, 2012, World Journal of Pediatrics.