(Q36834983)

16 August 2017

A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism (English)

1 reference

16 August 2017

1 reference

David S Geller

1

1 reference

16 August 2017

Junhui Zhang

2

1 reference

16 August 2017

Max V Wisgerhof

3

1 reference

16 August 2017

Cedric Shackleton

4

1 reference

16 August 2017

Michael Kashgarian

5

1 reference

16 August 2017

Richard P Lifton

6

1 reference

16 August 2017

language of work or name

English

0 references

publication date

27 May 2008

1 reference

The Journal of Clinical Endocrinology and Metabolism

16 August 2017

1 reference

16 August 2017

93

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16 August 2017

8

1 reference

16 August 2017

3117-3123

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Monogenic mineralocorticoid hypertension

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

DAX1 origin, function, and novel role

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

Stress hormone and male reproductive function

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

Diagnosis of primary aldosteronism: from screening to subtype differentiation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

A role for the NGFI-B family in adrenal zonation and adrenocortical disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

Primary aldosteronism: a new clinical entity

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

Steroidogenic factor 1: an essential mediator of endocrine development

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

Quantitation of cortisol and related 3-oxo-4-ene steroids in urine using gas chromatography/mass spectrometry with stable isotope-labeled internal standards.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

Defective fasciculata zone function as the mechanism of glucocorticoid-remediable aldosteronism

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

Examination of chromosome 7p22 candidate genes RBaK, PMS2 and GNA12 in familial hyperaldosteronism type II.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2515083

Non-glucocorticoid-remediable aldosteronism in an infant with low-renin hypertension

5 September 2018

1 reference

12 December 2020

Familial hyperaldosteronism, not suppressed by dexamethasone

1 reference

12 December 2020

Elevated urinary excretion of 18-oxocortisol in glucocorticoid-suppressible aldosteronism

1 reference

12 December 2020

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

1 reference

12 December 2020

Mass spectrometry in the diagnosis of steroid-related disorders and in hypertension research

1 reference

12 December 2020

Evaluation of the dexamethasone suppression test for the diagnosis of glucocorticoid-remediable aldosteronism

1 reference

12 December 2020

Primary aldosteronism due to adrenal hyperplasia; occurrence in a boy aged 10 years

1 reference

12 December 2020

Identifiers

DOI

10.1210/JC.2008-0594

1 reference

16 August 2017

1 reference

16 August 2017

1 reference