A genetic defect resulting in mild low-renin hypertension (Q24669744)

Europe PubMed Central

title

A genetic defect resulting in mild low-renin hypertension (English)

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main subject

arterial hypertension

1 reference

P Ferrari

6

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author name string

R C Wilson

1

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S Dave-Sharma

2

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J Q Wei

3

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V R Obeyesekere

4

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K Li

5

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Z S Krozowski

7

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C H Shackleton

8

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L Bradlow

9

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T Wiens

10

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M I New

Proceedings of the National Academy of Sciences of the United States of America

11

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language of work or name

English

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publication date

18 August 1998

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published in

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volume

95

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issue

17

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page(s)

10200-5

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cites work

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The mineralocorticoid receptor discriminates aldosterone from glucocorticoids independently of the 11 beta-hydroxysteroid dehydrogenase

28 September 2017

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Renal Capture and Oxidation of Cortisol in Man1

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Radioimmunoassay of Plasma 17-Hydroxypregnenolone

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21 January 2018

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12 December 2020

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Minealocorticoid receptors and 11 beta-steroid dehydrogenase activity in renal principal and intercalated cells

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Mineralocorticoid hypertension and congenital deficiency of 11 beta-hydroxysteroid dehydrogenase in a family with the syndrome of 'apparent' mineralocorticoid excess

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12 December 2020

The R337C mutation generates a high Km 11 beta-hydroxysteroid dehydrogenase type II enzyme in a family with apparent mineralocorticoid excess

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12 December 2020

Immunolocalization of NAD-dependent 11 beta-hydroxysteroid dehydrogenase in human kidney and colon

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12 December 2020

Diagnosis and treatment of a child with the syndrome of apparent mineralocorticoid excess type 1

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12 December 2020

Hypertension in a four-year-old child: gas chromatographic and mass spectrometric evidence for deficient hepatic metabolism of steroids

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12 December 2020

Low-renin, low-aldosterone hypertension and abnormal cortisol metabolism in a 19-month-old child

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12 December 2020

Apparent mineralocorticoid excess and deficient 11 beta-oxidation of cortisol in a young female

1 reference

12 December 2020

Congenital 11 beta-hydroxysteroid dehydrogenase deficiency associated with juvenile hypertension: corticosteroid metabolite profiles of four patients and their families

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12 December 2020

The R337C mutation generates a high Km 11 beta-hydroxysteroid dehydrogenase type II enzyme in a family with apparent mineralocorticoid excess

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.17.10200

7 January 2021