Non-classic adrenal hyperplasia in hyperandrogenism: a reappraisal (Q77687831)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9854689%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

review article

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title

Non-classic adrenal hyperplasia in hyperandrogenism: a reappraisal (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9854689%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

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C Morán

1

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7 December 2019

E S Knochenhauer

series ordinal

2

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7 December 2019

R Azziz

series ordinal

3

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7 December 2019

publication date

1 November 1998

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Journal of Endocrinological Investigation

7 December 2019

published in

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7 December 2019

volume

21

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7 December 2019

page(s)

707-720

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7 December 2019

issue

10

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https://scigraph.springernature.com/pub.10.1007/bf03350803

7 December 2019

exact match

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cites work

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Is the inappropriate gonadotropin secretion of patients with polycystic ovary syndrome similar to that of patients with adult-onset congenital adrenal hyperplasia?

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Clinical and Molecular Genetics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

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Nonclassical 3β-hydroxysteroid dehydrogenase deficiency: a review of our experience with 25 female patients

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GH, ACTH, TSH, LH, and FSH Reserve in Prepubertal Girls with Congenital Adrenal Hyperplasia

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Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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High frequency of nonclassical steroid 21-hydroxylase deficiency

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Carriers of 21-hydroxylase deficiency are not at increased risk for hyperandrogenism.

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The Effect of Long Acting Glucocorticoids on Menstrual Abnormalities in Patients with Virilizing Congenital Adrenal Hyperplasia*

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Abnormalities of 21-hydroxylase gene ratio and adrenal steroidogenesis in hyperandrogenic women with an exaggerated 17-hydroxyprogesterone response to acute adrenal stimulation

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Ovarian suppression reduces clinical and endocrine expression of late-onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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Dynamics of 24-hour pulsatile cortisol, 17-hydroxyprogesterone, and androstenedione release in prepubertal patients with nonclassic 21-hydroxylase deficiency and normal prepubertal children

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Clinical review 56: Nonclassic adrenal hyperplasia: current concepts

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Absence of molecular defect in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrenal 3 beta-HSD activity

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Missense mutation serine106—-proline causes 17 alpha-hydroxylase deficiency

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Adrenocorticotropic hormone testing in idiopathic hirsutism and polycystic ovarian disease: a test of limited usefulness

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Late onset adrenal hyperplasia in a group of Irish females who presented with hirsutism, irregular menses and/or cystic acne

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Molecular abnormalities of the 21-hydroxylase gene in hyperandrogenic women with an exaggerated 17-hydroxyprogesterone response to short-term adrenal stimulation

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12 December 2020

On the origin of the elevated 17-hydroxyprogesterone levels after adrenal stimulation in hyperandrogenism

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12 December 2020

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

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12 December 2020

Assessment of the one hour adrenocorticotrophic hormone test in the diagnosis of attenuated 21-hydroxylase deficiency

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12 December 2020

Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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12 December 2020

The developmental changes in plasma adrenal androgens during infancy and adrenarche are associated with changing activities of adrenal microsomal 17-hydroxylase and 17,20-desmolase

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12 December 2020

Comparison of basal and adrenocorticotropin-stimulated plasma 21-deoxycortisol and 17-hydroxyprogesterone values as biological markers of late-onset adrenal hyperplasia

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12 December 2020

The incidence of late-onset congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency among hirsute women

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12 December 2020

Effects of individual mutations in the P-450(C21) pseudogene on the P-450(C21) activity and their distribution in the patient genomes of congenital steroid 21-hydroxylase deficiency

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A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.

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Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency

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Point mutations in Italian patients with classic, non-classic, and cryptic forms of steroid 21-hydroxylase deficiency

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Late-onset adrenal hyperplasia in north Indian hirsute women

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Pro-453 to Ser mutation in CYP21 is associated with nonclassic steroid 21-hydroxylase deficiency

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12 December 2020

Cyproterone acetate versus hydrocortisone treatment in late-onset adrenal hyperplasia

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12 December 2020

Dexamethasone preparation does not alter corticoid and androgen responses to adrenocorticotropin

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12 December 2020

Studies of 3 beta-hydroxysteroid dehydrogenase genes in infants and children manifesting premature pubarche and increased adrenocorticotropin-stimulated delta 5-steroid levels

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12 December 2020

The Incidence of Late-Onset Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency among Hirsute Women*

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12 December 2020

Characterisation of CAH alleles with non-radioactive DNA single strand conformation polymorphism analysis of the CYP21 gene

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12 December 2020

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

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12 December 2020

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Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data*

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12 December 2020

The detection of the heterozygous carrier for congenital virilizing adrenal hyperplasia

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12 December 2020

Clinical review 54: Genetics, diagnosis, and management of 21-hydroxylase deficiency

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12 December 2020

CYP11B1 mutations causing non-classic adrenal hyperplasia due to 11 beta-hydroxylase deficiency

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12 December 2020

Effects of continued adrenocorticotropin stimulation on the mineralocorticoid hormones in classical and nonclassical simple virilizing types of 21-hydroxylase deficiency

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12 December 2020

Fertility in women with late-onset adrenal hyperplasia due to 21-hydroxylase deficiency

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12 December 2020

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Late-onset congenital adrenal hyperplasia in women with hirsutism

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12 December 2020

Maternal side effects of prenatal dexamethasone therapy for fetal congenital adrenal hyperplasia

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12 December 2020

Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylase

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12 December 2020

The hypothalamic-pituitary-adrenal axis in partial (late-onset) 21-hydroxylase deficiency

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12 December 2020

Interactions of small nuclear RNA's with precursor messenger RNA during in vitro splicing

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12 December 2020

21-Hydroxylase deficiency in female hyperandrogenism: screening and diagnosis.

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12 December 2020

No evidence of mutations in the genes for type I and type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) in nonclassical 3 beta HSD deficiency

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12 December 2020

Identifiers

DOI

10.1007/BF03350803

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9854689%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

7 December 2019

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