Overview of Monogenic or Mendelian Forms of Hypertension

Pathogenesis of Familial Hyperaldosteronism Type II: New Concepts Involving Anion Channels

(2019) Michael Stowasser et al.   CURRENT HYPERTENSION REPORTS

Heart Disease and Stroke Statistics—2018 Update: A Report From the American Heart Association

(2018) Emelia J. Benjamin et al.   CIRCULATION

CLCN2 chloride channel mutations in familial hyperaldosteronism type II

(2018) Ute I. Scholl et al.   NATURE GENETICS

Hypertension Among Youths — United States, 2001–2016

(2018) Sandra L. Jackson et al.   MMWR-MORBIDITY AND MORTALITY WEEKLY REPORT

Is There a Role for Genomics in the Management of Hypertension?

(2017) Jacopo Burrello et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Treatment of Cervical Artery Dissection: Antithrombotics, Thrombolysis, and Endovascular Therapy

(2017) Jing Peng et al.   Biomed Research International

Liddle syndrome: clinical and genetic profiles

(2016) Yunying Cui et al.   Journal of Clinical Hypertension

Genetic and Molecular Aspects of Hypertension

(2015) S. Padmanabhan et al.   CIRCULATION RESEARCH

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

(2015) Lin-Ping Wang et al.   Journal of Clinical Hypertension

The World Heart Federation's vision for worldwide cardiovascular disease prevention

(2015) Salim Yusuf et al.   LANCET

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

(2015) Ute I Scholl et al.   eLife

Pheochromocytoma and Paraganglioma: An Endocrine Society Clinical Practice Guideline

(2014) Jacques W. M. Lenders et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Gordon Syndrome: a continuing story

(2014) Kevin M. O’Shaughnessy   PEDIATRIC NEPHROLOGY

Genes for blood pressure: an opportunity to understand hypertension

(2013) Georg B. Ehret et al.   EUROPEAN HEART JOURNAL

11Beta-Hydroxylase Deficiency and Other Syndromes of Mineralocorticoid Excess as a Rare Cause of Endocrine Hypertension

(2012) E. Melcescu et al.   HORMONE AND METABOLIC RESEARCH

Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas

(2012) Jenny Welander et al.   HUMAN MOLECULAR GENETICS

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

(2012) Lynn M. Boyden et al.   NATURE

Monogenic forms of hypertension

(2011) Giacomo Domenico Simonetti et al.   EUROPEAN JOURNAL OF PEDIATRICS

An Unusual Case of Metabolic Alkalosis: A Window Into the Pathophysiology and Diagnosis of This Common Acid-Base Disturbance

(2010) F. John Gennari et al.   AMERICAN JOURNAL OF KIDNEY DISEASES

High Prevalence of Liddle Syndrome Phenotype Among Hypertensive US Veterans in Northwest Louisiana

(2010) Mihály Tapolyai et al.   Journal of Clinical Hypertension

Genetic Analyses of the ChimericCYP11B1/CYP11B2Gene in a Korean Family with Glucocorticoid-Remediable Aldosteronism

(2010) Ihn Suk Lee et al.   JOURNAL OF KOREAN MEDICAL SCIENCE

Clinical and Molecular Features of Type 1 Pseudohypoaldosteronism

(2009) Felix G. Riepe   HORMONE RESEARCH

Genetics of Hypertensive Syndrome

(2009) Alejandro Martinez-Aguayo et al.   Hormone Research in Paediatrics

Epithelial Sodium Channel

(2008) Bernard C. Rossier et al.   HYPERTENSION