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Apparent mineralocorticoid excess: comprehensive overview of molecular genetics

Journal of translational medicine, 2022-11, Vol.20 (1), p.500-500, Article 500

2022

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Value of D-dimer and C reactive protein in predicting inhospital death in acute aortic dissection

Heart (British Cardiac Society), 2013-08, Vol.99 (16), p.1192-1197

2013

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Sex difference in nocturnal blood pressure dipping in adolescents with varying degrees of adiposity

BMC pediatrics, 2024-05, Vol.24 (1), p.353-353, Article 353

2024

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

Kidney & blood pressure research, 2023-01, Vol.48 (1), p.568-577

2023

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Influence of omega-3 polyunsaturated fatty acid-supplementation on platelet aggregation in humans: A meta-analysis of randomized controlled trials

Atherosclerosis, 2013-02, Vol.226 (2), p.328-334

2013

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Association of interleukin-18 gene polymorphisms with Takayasu arteritis in a Chinese Han population

Chinese medical journal, 2020-10, Vol.133 (19), p.2315-2320

2020

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

Journal of clinical medicine, 2022-12, Vol.12 (1), p.23

2022

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Long-term blood pressure outcomes of patients with adrenal venous sampling-proven unilateral primary aldosteronism

Journal of human hypertension, 2020-06, Vol.34 (6), p.440-447

2020

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

Scientific reports, 2017-05, Vol.7 (1), p.2407-11, Article 2407

2017

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

Kidney & blood pressure research, 2020-07, Vol.45 (4), p.603-611

2020

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

iScience, 2023-12, Vol.26 (12), p.108421-108421, Article 108421

2023

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

Chinese medical journal, 2019-01, Vol.132 (2), p.127-134

2019

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

Genes, 2022-05, Vol.13 (5), p.864

2022

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Seasonal variation of ambulatory blood pressure in Chinese hypertensive adolescents

Frontiers in pediatrics, 2022-11, Vol.10, p.1022865-1022865

2022

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Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chinese Family

Kidney & blood pressure research, 2019-10, Vol.44 (5), p.942-949

2019

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

The journal of clinical hypertension (Greenwich, Conn.), 2015-11, Vol.17 (11), p.902-907

2015

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A novel frameshift mutation of epithelial sodium channel β-subunit leads to Liddle syndrome in an isolated case

Clinical endocrinology (Oxford), 2015-04, Vol.82 (4), p.611-614

2015

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Clinical characteristics of concurrent primary aldosteronism and renal artery stenosis: A retrospective case-control study

Clinical and experimental hypertension (1993), 2021-01, Vol.43 (1), p.7-12

2021

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Overview of Monogenic Forms of Hypertension Combined With Hypokalemia

Frontiers in pediatrics, 2021-01, Vol.8, p.543309-543309

2021

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Clinical Characteristics and Prognosis of End-stage Hypertrophic Cardiomyopathy

Chinese medical journal, 2015-06, Vol.128 (11), p.1483-1489

2015

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Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome

Clinical and experimental hypertension (1993), 2018-02, Vol.40 (2), p.107-111

2018

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

Molecular medicine reports, 2020-06, Vol.21 (6), p.2459-2465

2020

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

Frontiers in cardiovascular medicine, 2022-06, Vol.9, p.896564-896564

2022

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

Frontiers in pediatrics, 2021-12, Vol.9, p.785982-785982

2021

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Effect of Aging on Hardening Behavior of 15-5 PH Stainless Steel

Journal of iron and steel research, international, 2015-07, Vol.22 (7), p.607-614

2015

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Apparent mineralocorticoid excess: comprehensive overview of molecular genetics

Value of D-dimer and C reactive protein in predicting inhospital death in acute aortic dissection

Sex difference in nocturnal blood pressure dipping in adolescents with varying degrees of adiposity

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

Influence of omega-3 polyunsaturated fatty acid-supplementation on platelet aggregation in humans: A meta-analysis of randomized controlled trials

Association of interleukin-18 gene polymorphisms with Takayasu arteritis in a Chinese Han population

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

Long-term blood pressure outcomes of patients with adrenal venous sampling-proven unilateral primary aldosteronism

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

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

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

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

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

Seasonal variation of ambulatory blood pressure in Chinese hypertensive adolescents

Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chinese Family

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

A novel frameshift mutation of epithelial sodium channel β-subunit leads to Liddle syndrome in an isolated case

Clinical characteristics of concurrent primary aldosteronism and renal artery stenosis: A retrospective case-control study

Overview of Monogenic Forms of Hypertension Combined With Hypokalemia

Clinical Characteristics and Prognosis of End-stage Hypertrophic Cardiomyopathy

Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome

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

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

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

Effect of Aging on Hardening Behavior of 15-5 PH Stainless Steel

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