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Steroid 11 beta-hydroxylase deficiency and related disorders
scientific article published on 01 June 1994
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
review article
1 reference
stated in
Europe PubMed Central
title
Steroid 11 beta-hydroxylase deficiency and related disorders
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
author name string
White PC
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
Speiser PW
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
publication date
1 June 1994
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
published in
Endocrinology and Metabolism Clinics of North America
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
volume
23
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
page(s)
325-339
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
cites work
11 beta-hydroxylase deficiency in hyperandrogenism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
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Escape from Mineralocorticoid Excess: The Role of Angiotensin II
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of late-onset 11 beta-hydroxylase deficiency in hirsute patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of cDNA encoding steroid 11 beta-hydroxylase (P450c11)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
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The Product of the CYP11B2 Gene Is Required for Aldosterone Biosynthesis in the Human Adrenal Cortex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
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Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
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The Role of Calcium in the Stimulation of Aldosterone Production by Adrenocorticotropin, Angiotensin II, and Potassium in Isolated Glomerulosa Cells
1 reference
stated in
Crossref
reference URL
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7 January 2021
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Dependence of Aldosterone Stimulation in Adrenal Glomerulosa Cells on Calcium Uptake: Effects of Lanthanum and Verapamil
1 reference
stated in
Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal treatment in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: up-date 88 of the French multicentric study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
19-Nor-Deoxycorticosterone Excretion in Primary Aldosteronism and Low Renin Hypertension*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning and expression of a cDNA for human cytochrome P-450aldo as related to primary aldosteronism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aldosterone secretion rate in the hypertensive form of congenital adrenal hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
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Normative Data for Adrenal Steroidogenesis in a Healthy Pediatric Population: Age- and Sex-Related Changes after Adrenocorticotropin Stimulation*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
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Fertility rates in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Therapeutic effect of calcium channel blockade in primary aldosteronism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Secretion rates of cortisol and aldosterone precursors in various forms of congenital adrenal hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
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Adrenal glomerulosa function in patients with dexamethasone-suppressible hyperaldosteronism
1 reference
stated in
Crossref
reference URL
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7 January 2021
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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
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
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7 January 2021
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Hormonal Studies in Obligate Heterozygotes and Siblings of Patients with l1/?-Hydroxylase Deficiency Congenital Adrenal Hyperplasia*
1 reference
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Crossref
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7 January 2021
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Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency
1 reference
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Crossref
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7 January 2021
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Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2
1 reference
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Crossref
reference URL
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7 January 2021
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Calcium, the renin-aldosterone system, and the hypotensive response to nifedipine
1 reference
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7 January 2021
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Cellular calcium and magnesium metabolism in the pathophysiology and treatment of hypertension and related metabolic disorders
1 reference
stated in
Crossref
reference URL
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7 January 2021
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11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
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7 January 2021
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High frequency of congenital adrenal hyperplasia (classic 11 beta-hydroxylase deficiency) among Jews from Morocco
1 reference
stated in
Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
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7 January 2021
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Defective fasciculata zone function as the mechanism of glucocorticoid-remediable aldosteronism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
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
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
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7 January 2021
based on heuristic
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Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2818%2930100-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0889-8529(18)30100-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
PubMed publication ID
8070425
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8070425
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8070425%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
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