(Q36635042)

15 August 2017

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title

Monogenic forms of low-renin hypertension (English)

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15 August 2017

1

Vesna D Garovic

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15 August 2017

Anthony A Hilliard

2

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15 August 2017

Stephen T Turner

series ordinal

3

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15 August 2017

publication date

1 November 2006

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Nature Clinical Practice Nephrology

15 August 2017

published in

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15 August 2017

volume

2

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15 August 2017

issue

11

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15 August 2017

page(s)

624-630

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Glucocorticoid-remediable aldosteronism in a large kindred: clinical spectrum and diagnosis using a characteristic biochemical phenotype

15 August 2017

cites work

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

Large-scale search for genes predisposing to essential hypertension

21 January 2018

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Genome scans for hypertension and blood pressure regulation

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Primary aldosteronism and hypertensive disease

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Diagnosis of primary aldosteronism: from screening to subtype differentiation

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Screening for primary aldosteronism in essential hypertension: diagnostic accuracy of the ratio of plasma aldosterone concentration to plasma renin activity

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Validity of plasma aldosterone-to-renin activity ratio in African American and white subjects with resistant hypertension

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Investigation of hypertension and the recognition of monogenic hypertension

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Familial hyperaldosteronism type II: five families with a new variety of primary aldosteronism

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Monogenic low renin hypertension

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Mineralocorticoids in congenital adrenal hyperplasia

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

The severe form of hypertension caused by the activating S810L mutation in the mineralocorticoid receptor is cortisone related.

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Licorice inhibits 11 beta-hydroxysteroid dehydrogenase messenger ribonucleic acid levels and potentiates glucocorticoid hormone action

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7 January 2021

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome

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7 January 2021

https://api.crossref.org/works/10.1038%2FNCPNEPH0309

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7 January 2021

Human hypertension caused by mutations in WNK kinases

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl- -transporting epithelia

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

WNK4 regulates the balance between renal NaCl reabsorption and K+ secretion

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https://api.crossref.org/works/10.1038%2FNCPNEPH0309

7 January 2021

P450c17 deficiency in Brazilian patients: biochemical diagnosis through progesterone levels confirmed by CYP17 genotyping

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7 January 2021

Identifiers

DOI

10.1038/NCPNEPH0309

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15 August 2017

1 reference