Steroid 11 beta-hydroxylase deficiency and related disorders (Q72150336)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425 AND SRC:MED&resulttype=core&format=json

24 October 2019

review article

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title

Steroid 11 beta-hydroxylase deficiency and related disorders (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425 AND SRC:MED&resulttype=core&format=json

24 October 2019

author name string

White PC

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425 AND SRC:MED&resulttype=core&format=json

24 October 2019

Speiser PW

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425 AND SRC:MED&resulttype=core&format=json

24 October 2019

publication date

1 June 1994

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425 AND SRC:MED&resulttype=core&format=json

Endocrinology and Metabolism Clinics of North America

24 October 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425 AND SRC:MED&resulttype=core&format=json

24 October 2019

volume

23

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24 October 2019

issue

2

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24 October 2019

page(s)

325-339

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425 AND SRC:MED&resulttype=core&format=json

11 beta-hydroxylase deficiency in hyperandrogenism

24 October 2019

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Prevalence of late-onset 11 beta-hydroxylase deficiency in hirsute patients

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Cloning of cDNA encoding steroid 11 beta-hydroxylase (P450c11)

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The Product of the CYP11B2 Gene Is Required for Aldosterone Biosynthesis in the Human Adrenal Cortex

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Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8

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The Role of Calcium in the Stimulation of Aldosterone Production by Adrenocorticotropin, Angiotensin II, and Potassium in Isolated Glomerulosa Cells

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Dependence of Aldosterone Stimulation in Adrenal Glomerulosa Cells on Calcium Uptake: Effects of Lanthanum and Verapamil

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Prenatal treatment in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: up-date 88 of the French multicentric study

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19-Nor-Deoxycorticosterone Excretion in Primary Aldosteronism and Low Renin Hypertension*

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Cloning and expression of a cDNA for human cytochrome P-450aldo as related to primary aldosteronism

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Aldosterone secretion rate in the hypertensive form of congenital adrenal hyperplasia

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

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

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Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients

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7 January 2021

Fertility rates in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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7 January 2021

Therapeutic effect of calcium channel blockade in primary aldosteronism

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Secretion rates of cortisol and aldosterone precursors in various forms of congenital adrenal hyperplasia

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Adrenal glomerulosa function in patients with dexamethasone-suppressible hyperaldosteronism

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Production of 19-oic-11-deoxycorticosterone from 19-oxo-11-deoxycorticosterone by cytochrome P-450(11)beta and nonenzymatic production of 19-nor-11-deoxycorticosterone from 19-oic-11-deoxycorticosterone

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Hormonal Studies in Obligate Heterozygotes and Siblings of Patients with l1/?-Hydroxylase Deficiency Congenital Adrenal Hyperplasia*

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Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency

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7 January 2021

Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2

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7 January 2021

Calcium, the renin-aldosterone system, and the hypotensive response to nifedipine

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7 January 2021

11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis

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High frequency of congenital adrenal hyperplasia (classic 11 beta-hydroxylase deficiency) among Jews from Morocco

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7 January 2021

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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7 January 2021

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

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

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Further studies on the treatment of congenital adrenal hyperplasia with cortisone. III. The control of hypertension with cortisone, with a discussion of variations in the type of congenital adrenal hyperplasia and report of a case with probable defe

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7 January 2021

Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients

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7 January 2021

10.1016/S0889-8529(18)30100-2

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425 AND SRC:MED&resulttype=core&format=json

24 October 2019

1 reference