Lin-ping Wang

Chinese Academy Of Medical Sciences And Peking Union Medical College
Beijing, China

Last Updated: 09/26/2026

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Found 12 publications

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

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

Journal: Endocrine

Published: May 06, 2020

Prevalence and Clinical Characteristics of Fabry Disease in Chinese Patients With Hypertrophic Cardiomyopathy.

Prevalence and Clinical Characteristics of Fabry Disease in Chinese Patients With Hypertrophic Cardiomyopathy.

Journal: The American journal of the medical sciences

Published: March 26, 2020

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

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

Journal: American journal of hypertension

Published: February 18, 2020

Tuberculosis in Takayasu arteritis: a retrospective study in 1105 Chinese patients.

Tuberculosis in Takayasu arteritis: a retrospective study in 1105 Chinese patients.

Journal: Journal of geriatric cardiology : JGC

Published: September 27, 2019

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

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

Journal: Molecular medicine reports

Published: July 11, 2019

A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation.

A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation.

Journal: Scientific reports

Published: March 06, 2017

Left Ventricular Noncompaction in Older Patients.

Left Ventricular Noncompaction in Older Patients.

Journal: The American journal of the medical sciences

Published: December 11, 2016

Lack of association between polymorphisms in interleukin (IL)-12, IL-12R, IL-23, IL-23R genes and Takayasu arteritis in a Chinese population.

Lack of association between polymorphisms in interleukin (IL)-12, IL-12R, IL-23, IL-23R genes and Takayasu arteritis in a Chinese population.

Journal: Inflammation research : official journal of the European Histamine Research Society ... [et al.]

Published: December 10, 2015

Coenzyme Q10 treatment of cardiovascular disorders of ageing including heart failure, hypertension and endothelial dysfunction.

Coenzyme Q10 treatment of cardiovascular disorders of ageing including heart failure, hypertension and endothelial dysfunction.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: May 24, 2015

Prevalence of Liddle Syndrome Among Young Hypertension Patients of Undetermined Cause in a Chinese Population.

Prevalence of Liddle Syndrome Among Young Hypertension Patients of Undetermined Cause in a Chinese Population.

Journal: Journal of clinical hypertension (Greenwich, Conn.)

Published: February 24, 2015

Clinical Profile and Prognosis of Left Ventricular Apical Aneurysm in Hypertrophic Cardiomyopathy.

Clinical Profile and Prognosis of Left Ventricular Apical Aneurysm in Hypertrophic Cardiomyopathy.

Journal: The American journal of the medical sciences

Published: January 15, 2015

Genetic diagnosis of Liddle's syndrome by mutation analysis of SCNN1B and SCNN1G in a Chinese family.

Genetic diagnosis of Liddle's syndrome by mutation analysis of SCNN1B and SCNN1G in a Chinese family.

Journal: Chinese medical journal

Published: May 23, 2012

Showing 1-12 of 12

Last Updated: 09/26/2026