Di Zhang

发表

Anemia in patients with Takayasu arteritis: prevalence, clinical features, and treatment

Li-sheng Liu, F. Luo, Xian-liang Zhou, 2019, Journal of geriatric cardiology : JGC.

Quantitative protein profiling of hippocampus during human aging

Wenying Qiu, Chao Ma, Qian Yang, 2016, Neurobiology of Aging.

Blood manganese and nonalcoholic fatty liver disease: A cohort-based case-control study.

Shuohua Chen, Shouling Wu, Yanhong Wang, 2021, Chemosphere.

Hypertension and brachydactyly syndrome associated with vertebral artery malformation caused by a PDE3A missense mutation.

F. Luo, Xian-liang Zhou, Lei Song, 2019, American journal of hypertension.

Implication of a novel truncating mutation in titin as a cause of autosomal dominant left ventricular noncompaction

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

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.

Severe right ventricular hypertrophy in hypertrophic cardiomyopathy: Serious symptoms, complex surgical procedures, and poor prognosis in Fuwai Hospital.

Xian-liang Zhou, Ya-xin Liu, Xu Meng, 2021, Anatolian journal of cardiology.

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.

Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report

F. Luo, Ya-xin Liu, T. Tian, 2020, Molecular medicine reports.

A novel phenotype with splicing mutation identified in a Chinese family with desminopathy

K. Dou, Xue Zhang, Ya-xin Liu, 2019, Chinese medical journal.

Overview of Monogenic Forms of Hypertension Combined With Hypokalemia

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

Prognostic Value and Optimal Candidates of Primary Tumor Surgery in Metastatic Adenoid Cystic Carcinoma of the Head and Neck: First Evidence from a Population-Based Study

Di Zhang, 2021 .

A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia

F. Luo, Wen-jun Ma, Jun Cai, 2019, American journal of hypertension.

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.

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.

Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension

F. Luo, Wen-jun Ma, Jun Cai, 2020, American journal of hypertension.

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.

Liddle syndrome misdiagnosed as primary aldosteronism resulting from a novel frameshift mutation of SCNN1B

F. Luo, Xue Zhang, Jun Cai, 2018, Endocrine connections.

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.

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

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

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.

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.

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

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