Yi-ting Lu

发表

Apparent mineralocorticoid excess: comprehensive overview of molecular genetics

Xian-liang Zhou, Di Zhang, Ze-Ming Zhou, 2022, Journal of Translational Medicine.

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.

Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation

Xian-liang Zhou, Lei Song, Wen-jun Ma, 2020, Kidney and Blood Pressure Research.

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.

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.

Widely Association Analysis and Identification New Early-Onset Factor for Prediction of Coronary Heart Disease

Jindong Ren, Yi-Ting Lu, Lizhi Lu, 2018 .

Overview of Monogenic Forms of Hypertension Combined With Hypokalemia

Xu Meng, P. Fan, Lin Zhao, 2021, Frontiers in Pediatrics.

RET c.1901G>A and Novel SLC12A3 Mutations in Familial Pheochromocytomas

Xian-liang Zhou, Kunqi Yang, Xu Meng, 2022, Genes.

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.

Prognostic value of plasma big endothelin-1 in left ventricular non-compaction cardiomyopathy

F. Luo, Xian-liang Zhou, Kunqi Yang, 2020, Heart.

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.

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.

Apparent mineralocorticoid excess caused by novel compound heterozygous mutations in HSD11B2 and characterized by early-onset hypertension and hypokalemia

F. Luo, Wen-jun Ma, Jun Cai, 2020, Endocrine.

Childhood-Onset Refractory Hypertension Results from Neurofibromatosis Type 1 Caused by a Splicing NF1 Mutation

T. Tian, P. Fan, Di Zhang, 2023, Kidney and Blood Pressure Research.

Predicting stroke and myocardial infarction risk in Takayasu arteritis with automated machine learning models

T. Tian, P. Fan, Ying Zhang, 2023, iScience.