(Q35574187)

8 August 2017

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title

Hypertension and adrenal disorders (English)

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8 August 2017

Wassim Chemaitilly

1

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8 August 2017

Robert C Wilson

series ordinal

2

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8 August 2017

Maria I New

series ordinal

3

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8 August 2017

publication date

1 December 2003

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Current Hypertension Reports

8 August 2017

published in

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8 August 2017

volume

5

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8 August 2017

issue

6

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8 August 2017

page(s)

498-504

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A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin

8 August 2017

cites work

1 reference

12 December 2020

Male pseudohermaphroditism due to 17α-hydroxylase deficiency

1 reference

12 December 2020

A genetic defect resulting in mild low-renin hypertension

1 reference

12 December 2020

Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess

1 reference

12 December 2020

Phaeochromocytoma and paraganglioma

1 reference

12 December 2020

New therapeutic and surgical approaches for sporadic and hereditary pheochromocytoma

1 reference

12 December 2020

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

1 reference

12 December 2020

The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization

1 reference

12 December 2020

[Pheochromocytoma: pediatric features]

1 reference

12 December 2020

Familial/sporadic glucocorticoid resistance syndrome and hypertension

1 reference

12 December 2020

Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess

1 reference

12 December 2020

Localization of the human CYP17 gene (cytochrome P450(17 alpha)) to 10q24.3 by fluorescence in situ hybridization and simultaneous chromosome banding

1 reference

12 December 2020

Congenital adrenal hyperplasia: 11beta-hydroxylase deficiency

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12 December 2020

Pheochromocytoma: an approach to antihypertensive management

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12 December 2020

Diagnostic tests for Cushing's syndrome

1 reference

12 December 2020

Hypertension in congenital adrenal hyperplasia and apparent mineralocorticoid excess

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12 December 2020

The diagnosis and management of endocrine tumors causing hypertension in children

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12 December 2020

The medical management of Cushing's syndrome

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12 December 2020

Glucocorticoid-remediable aldosteronism.

1 reference

12 December 2020

New advances in the biochemical diagnosis of pheochromocytoma: moving beyond catecholamines

1 reference

12 December 2020

Clinical and genetic aspects of phaeochromocytoma

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12 December 2020

Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia

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12 December 2020

Minireview: Primary Aldosteronism—Changing Concepts in Diagnosis and Treatment

1 reference

12 December 2020

Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertension

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12 December 2020

Leptin and the central neural mechanisms of obesity hypertension

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12 December 2020

Regulation of catecholamine synthesis by leptin

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12 December 2020

Aldo is back: recent advances and unresolved controversies in hyperaldosteronism

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12 December 2020

Diagnosis and management of congenital adrenal hyperplasia.

1 reference

12 December 2020

10.1007/S11906-003-0058-1

Identifiers

DOI

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8 August 2017

1 reference