(Q74425274)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9536212%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

review article

1 reference

title

Congenital adrenal hyperplasia (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9536212%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

S Pang

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9536212%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

publication date

1 June 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9536212%20AND%20SRC:MED&resulttype=core&format=json

Bailliere's clinical obstetrics and gynaecology

10 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9536212%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9536212%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9536212%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

281-306

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9536212%20AND%20SRC:MED&resulttype=core&format=json

The incidence of non-classical 21-hydroxylase deficiency in hirsute adolescent girls

10 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Clinical review 56: Nonclassic adrenal hyperplasia: current concepts

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Congenital Adrenal Hyperplasia and Fertility

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

The response of several adrenocortical steroids to the administration of ACTH in hirsute women

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

The adrenogenital syndrome with deficiency of 3 beta-hydroxysteroid dehydrogenase

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Elevated 17-hydroxyprogesterone and testosterone in a newborn with 3-beta-hydroxysteroid dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Difference in transcriptional activity of two homologous CYP21A genes

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Mutations in the type II 3 beta-hydroxysteroid dehydrogenase gene in a patient with classic salt-wasting 3 beta-hydroxysteroid dehydrogenase deficiency congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Clinical and biological phenotypes in late-onset 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Detection of Functional Ovarian Hyperandrogenism in Women with Androgen Excess

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Secondary biosynthetic defects in women with late-onset congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Increased plasma 21-deoxycorticosterone (21-DB) levels in late-onset adrenal 21-hydroxylase deficiency suggest a mild defect of the mineralocorticoid pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

The application of a new highly-sensitive radioimmunoassay for plasma 21-deoxycortisol to the detection of steroid-21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Linear growth and pubertal development in treated congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Abnormal Adrenal Responses to Adrenocorticotropic Hormone in Hyperandrogenic Women

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Adrenal insufficiency in a man with non-classical 21-hydroxylase deficiency: consequence or coincidence?

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Steroid responses to ACTH in women with polycystic ovaries

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Subnormal androgen and elevated progesterone levels in women treated for congenital virilizing 21-hydroxylase deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Menstrual disturbance and hypersecretion of progesterone in women with congenital adrenal hyperplasia due to 21‐hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Congenital adrenal hyperplasia: age at menarche and related events at puberty.

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Serum gonadotropin levels in female adolescents with congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Gonadotropin Output in Congenital Adrenal Hyperplasia before and after Adrenal Suppression

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Glucocorticoid treatment of girls with congenital adrenal hyperplasia: effects on height, sexual maturation, and fertility

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Late-Onset Steroid 21-Hydroxylase Deficiency: A Variant of Classical Congenital Adrenal Hyperplasia*

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

The 21-Hydroxylase Activity in the Glomerulosa and Fasciculata of the Adrenal Cortex in Congenital Adrenal Hyperplasia*

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Late-onset adrenal hyperplasia in hirsutism

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Structure, function and tissue-specific gene expression of 3β-hydroxysteroid dehydrogenase/5-ene-4-ene isomerase enzymes in classical and peripheral intracrine steroidogenic tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Evidence for Reduced 3β-ol-Hydroxysteroid Dehydrogenase Activity in Some Hirsute Women Thought to Have Poly cystic Ovary Syndrome*

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Studies of the C-21 and C-19 Steroids and HLA Genotyping in Siblings and Parents of Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency*

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

The 3beta-hydroxysteroid dehydrogenase gene family of enzymes

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Male pseudohermaphroditism due to nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency: gender role change and absence of gynecomastia at puberty

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Mutation in 3 beta-hydroxysteroid dehydrogenase type II associated with pseudohermaphroditism in males and premature pubarche or cryptic expression in females

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Molecular and clinical advances in congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data*

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Serum androgen concentrations in neonates and young infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Nonsalt-Losing Congenital Adrenal Hyperplasia due to 3β-Hydroxysteroid Dehydrogenase Deficiency with Normal Glomerulosa Function*

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Late-onset adrenal steroid 3 beta-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

The Response of Pituitary Gonadotropes to Synthetic LRF in Children with Glucocorticoid-Treated Congenital Adrenal Hyperplasia: Lack of Effect of Intrauterine and Neonatal Androgen Excess

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Congenital adrenal hyperplasia due to point mutations in the type II 3 beta-hydroxysteroid dehydrogenase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Molecular basis of congenital adrenal hyperplasia in two siblings with classical nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Pubertal Presentation of Congenital Δ5–-3β–Hydroxysteroid Dehydrogenase Deficiency*

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Mutation in the human gene for 3 beta-hydroxysteroid dehydrogenase type II leading to male pseudohermaphroditism without salt loss

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Functional characterization of the novel L108W and P186L mutations detected in the type II 3 beta-hydroxysteroid dehydrogenase gene of a male pseudohermaphrodite with congenital adrenal hyperplasia.

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Detection and functional characterization of the novel missense mutation Y254D in type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) gene of a female patient with nonsalt-losing 3 beta HSD deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Persistent testicular delta5-isomerase-3beta-hydroxysteroid dehydrogenase (delta5-3beta-HSD) deficiency in the delta5-3beta-HSD form of congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Molecular basis of congenital adrenal hyperplasia due to 3 beta- hydroxysteroid dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Congenital adrenal hyperplasia caused by a novel homozygous frameshift mutation 273 delta AA in type II 3 beta-hydroxysteroid dehydrogenase gene (HSD3B2) in three male patients of Afghan/Pakistani origin

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Cyproterone acetate versus hydrocortisone treatment in late-onset adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Genetic defects of steroidogenesis in premature pubarche

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Investigation of adrenal function in women with oligomenorrhoea and hirsutism (clinical PCOS) from the north-east of England using an adrenal stimulation test

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

3&beta;-Hydroxysteroid Dehydrogenase Deficiency Follow-Up Study in a Girl with Pubertal Bone Age

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

Prevalence of nonclassical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: a small sample study

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3552%2897%2980038-7

7 January 2021

10.1016/S0950-3552(97)80038-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9536212%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference