Diagnosis and Treatment of Monogenic Hypertension in Children

Overview of Monogenic Forms of Hypertension Combined With Hypokalemia

(2021) Yi-Ting Lu et al.   Frontiers in Pediatrics

Genomics of hypertension: the road to precision medicine

(2020) Sandosh Padmanabhan et al.   Nature Reviews Cardiology

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

(2019) Michael Stowasser et al.   CURRENT HYPERTENSION REPORTS

Overview of Monogenic or Mendelian Forms of Hypertension

(2019) Rupesh Raina et al.   Frontiers in Pediatrics

An unexpected, mild phenotype of glucocorticoid resistance associated with glucocorticoid receptor gene mutation case report and review of the literature

(2018) Ágnes Molnár et al.   BMC Medical Genetics

The Low-Renin Hypertension Phenotype: Genetics and the Role of the Mineralocorticoid Receptor

(2018) Rene Baudrand et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

CLCN2 chloride channel mutations in familial hyperaldosteronism type II

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

Cardiometabolic outcomes and mortality in medically treated primary aldosteronism: a retrospective cohort study

(2018) Gregory L Hundemer et al.   Lancet Diabetes & Endocrinology

Genetic Programming of Hypertension

(2018) Sun-Young Ahn et al.   Frontiers in Pediatrics

Hypertension in childhood obesity

(2018) Elke Wühl   ACTA PAEDIATRICA

Genetic Causes of Functional Adrenocortical Adenomas

(2017) Maria-Christina Zennaro et al.   ENDOCRINE REVIEWS

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

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

A Missense Mutation in the Extracellular Domain ofαENaC Causes Liddle Syndrome

(2017) Mahdi Salih et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Clinical Practice Guideline for Screening and Management of High Blood Pressure in Children and Adolescents

(2017) Joseph T. Flynn et al.   PEDIATRICS

Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency

(2017) Mabel Yau et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

WNK signalling pathways in blood pressure regulation

(2016) Meena Murthy et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Three Novel Heterozygous Point Mutations ofNR3C1Causing Glucocorticoid Resistance

(2016) Géraldine Vitellius et al.   HUMAN MUTATION

In Liddle Syndrome, Epithelial Sodium Channel Is Hyperactive Mainly in the Early Part of the Aldosterone-Sensitive Distal NephronNovelty and Significance

(2016) Viatcheslav Nesterov et al.   HYPERTENSION

The Management of Primary Aldosteronism: Case Detection, Diagnosis, and Treatment: An Endocrine Society Clinical Practice Guideline

(2016) John W. Funder et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

2016 European Society of Hypertension guidelines for the management of high blood pressure in children and adolescents

(2016) Empar Lurbe et al.   JOURNAL OF HYPERTENSION

CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism

(2016) Georgios Daniil et al.   EBioMedicine

Genetic and Molecular Aspects of Hypertension

(2015) S. Padmanabhan et al.   CIRCULATION RESEARCH

GENETICS OF PRIMARY ALDOSTERONISM

(2015) Anand Vaidya et al.   Endocrine Practice

An Update on Familial Hyperaldosteronism

(2015) H. Korah et al.   HORMONE AND METABOLIC RESEARCH

Understanding primary aldosteronism: impact of next generation sequencing and expression profiling

(2015) Silvia Monticone et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

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

(2015) Ute I Scholl et al.   eLife

Genetic Spectrum and Clinical Correlates of Somatic Mutations in Aldosterone-Producing Adenoma

(2014) Fabio Luiz Fernandes-Rosa et al.   HYPERTENSION

Heritability of blood pressure through latent curve trajectories in families from the Gubbio population study

(2014) Maria Teresa Bonati et al.   JOURNAL OF HYPERTENSION

Age-Related Changes in 11 -Hydroxysteroid Dehydrogenase Type 2 Activity in Normotensive Subjects

(2013) C. Campino et al.   AMERICAN JOURNAL OF HYPERTENSION

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

(2012) Lynn M. Boyden et al.   NATURE

Current concepts in glucocorticoid resistance

(2012) Nan Yang et al.   STEROIDS

Monogenic forms of hypertension

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

K+ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension

(2011) M. Choi et al.   SCIENCE

Relation of blood pressure and body mass index during childhood to cardiovascular risk factor levels in young adults

(2009) Erin R Rademacher et al.   JOURNAL OF HYPERTENSION

A Novel Form of Human Mendelian Hypertension Featuring Nonglucocorticoid-Remediable Aldosteronism

(2008) David S. Geller et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM