(Q38357343)

2 September 2017

High aldosterone-to-renin variants of CYP11B2 and pregnancy outcome (English)

1 reference

2 September 2017

1 reference

Geneviève Escher

1

1 reference

2 September 2017

Martino Cristiano

2

1 reference

2 September 2017

Maja Causevic

3

1 reference

2 September 2017

Marc Baumann

4

1 reference

2 September 2017

Felix J Frey

5

1 reference

2 September 2017

Daniel Surbek

6

1 reference

2 September 2017

Markus G Mohaupt

7

1 reference

2 September 2017

language of work or name

English

0 references

publication date

16 January 2009

1 reference

Nephrology Dialysis Transplantation

2 September 2017

1 reference

2 September 2017

24

1 reference

2 September 2017

6

1 reference

2 September 2017

1870-1875

1 reference

Long term mortality of mothers and fathers after pre-eclampsia: population based cohort study

2 September 2017

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Potassium regulation and progesterone-aldosterone interrelationships in human pregnancy: a prospective study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Control of sodium excretion in human pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Evidence for compromised aldosterone synthase enzyme activity in preeclampsia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

A biallelic gene polymorphism of CYP11B2 predicts increased aldosterone to renin ratio in selected hypertensive patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Blood-pressure measurement and classification in pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

An influence of variation in the aldosterone synthase gene (CYP11B2) on corticosteroid responses to ACTH in normal human subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Urinary tetrahydroaldosterone as a screening method for primary aldosteronism: a comparative study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Molecular genetics of human hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

The L10F mutation of angiotensinogen is rare in pre-eclampsia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Angiotensinogen: a candidate gene involved in preeclampsia?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Preeclampsia. Part 1: clinical and pathophysiologic considerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Pathogenesis and genetics of pre-eclampsia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Lack of association between the CYP11B2 gene polymorphism and preeclampsia, eclampsia, and the HELLP syndrome in Turkish women.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

The importance of genetic and environmental effects for pre-eclampsia and gestational hypertension: a family study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Variation at the aldosterone synthase (CYP11B2) locus contributes to hypertension in subjects with a raised aldosterone-to-renin ratio.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

The effect of oxygen on aldosterone release from bovine adrenocortical cells in vitro: PO2 versus steroidogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Analysis of the S810L point mutation of the mineralocorticoid receptor in patients with pregnancy-induced hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

Polymorphisms of thrombophilic and vasoactive genes and severe preeclampsia: a pilot study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN763

21 January 2018

Identifiers

DOI

10.1093/NDT/GFN763

1 reference

release_afb66pjyfjb2nhapuapce6wzw4

2 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/afb66pjyfjb2nhapuapce6wzw4

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference