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Congenital adrenal hyperplasia
scientific article published on 01 December 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9429863
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429863%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Congenital adrenal hyperplasia
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9429863
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429863%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
main subject
adrenal hyperplasia
1 reference
based on heuristic
inferred from title
author name string
S Pang
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9429863
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429863%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
publication date
1 December 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9429863
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429863%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
published in
Endocrinology and Metabolism Clinics of North America
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9429863
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429863%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
volume
26
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9429863
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429863%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9429863
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429863%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
page(s)
853-891
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9429863
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429863%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
cites work
Clinical review 56: Nonclassic adrenal hyperplasia: current concepts
1 reference
stated in
Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormalities of 21-hydroxylase gene ratio and adrenal steroidogenesis in hyperandrogenic women with an exaggerated 17-hydroxyprogesterone response to acute adrenal stimulation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
The adrenogenital syndrome with deficiency of 3 beta-hydroxysteroid dehydrogenase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The pathophysiology and genetics of congenital lipoid adrenal hyperplasia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Elevated 17-hydroxyprogesterone and testosterone in a newborn with 3-beta-hydroxysteroid dehydrogenase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ovarian suppression reduces clinical and endocrine expression of late-onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Difference in transcriptional activity of two homologous CYP21A genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and biological phenotypes in late-onset 21-hydroxylase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal dexamethasone treatment in pregnancies at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency: effect on midgestational amniotic fluid steroid levels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of Functional Ovarian Hyperandrogenism in Women with Androgen Excess
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Secondary biosynthetic defects in women with late-onset congenital adrenal hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The hypothalamic-pituitary-adrenal axis in partial (late-onset) 21-hydroxylase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Increased plasma 21-deoxycorticosterone (21-DB) levels in late-onset adrenal 21-hydroxylase deficiency suggest a mild defect of the mineralocorticoid pathway
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The application of a new highly-sensitive radioimmunoassay for plasma 21-deoxycortisol to the detection of steroid-21-hydroxylase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pitfalls in prenatal diagnosis of 21-hydroxylase deficiency by amniotic fluid steroid analysis? A six years experience in 102 pregnancies at risk
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal Adrenal Responses to Adrenocorticotropic Hormone in Hyperandrogenic Women
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adrenal insufficiency in a man with non-classical 21-hydroxylase deficiency: consequence or coincidence?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Steroid responses to ACTH in women with polycystic ovaries
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel missense mutation in the type II 3β-hydroxysteroid dehydrogenase gene in a family with classical salt-wasting congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glucocorticoid treatment of girls with congenital adrenal hyperplasia: effects on height, sexual maturation, and fertility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Late-Onset Steroid 21-Hydroxylase Deficiency: A Variant of Classical Congenital Adrenal Hyperplasia*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Serum Androgens as a Continuing Index of Adequacy of Treatment of Congenital Adrenal Hyperplasia*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The 21-Hydroxylase Activity in the Glomerulosa and Fasciculata of the Adrenal Cortex in Congenital Adrenal Hyperplasia*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Late-onset adrenal hyperplasia in hirsutism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A preliminary study of flutamide, testolactone, and reduced hydrocortisone dose in the treatment of congenital adrenal hyperplasia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal diagnosis and treatment of congenital adrenal hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New Studies of the llβ-Hydroxylase and 18-Hydroxylase Enzymes in the Hypertensive Form of Congenital Adrenal Hyperplasia*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for Reduced 3β-ol-Hydroxysteroid Dehydrogenase Activity in Some Hirsute Women Thought to Have Poly cystic Ovary Syndrome*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The 3beta-hydroxysteroid dehydrogenase gene family of enzymes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Male pseudohermaphroditism due to nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency: gender role change and absence of gynecomastia at puberty
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in 3 beta-hydroxysteroid dehydrogenase type II associated with pseudohermaphroditism in males and premature pubarche or cryptic expression in females
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular and clinical advances in congenital adrenal hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Magnetic resonance imaging in the congenital adrenal hyperplasia population: increased frequency of white-matter abnormalities and temporal lobe atrophy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital adrenal hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Newborn screening and its relationship to the diagnosis and treatment of the disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Late-onset adrenal steroid 3 beta-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amniotic fluid concentrations of delta 5 and delta 4 steroids in fetuses with congenital adrenal hyperplasia due to 21 hydroxylase deficiency and in anencephalic fetuses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Serum androgen concentrations in neonates and young infants 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%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nonsalt-Losing Congenital Adrenal Hyperplasia due to 3β-Hydroxysteroid Dehydrogenase Deficiency with Normal Glomerulosa Function*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and characterization of the G15D mutation found in a male patient with 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) deficiency: alteration of the putative NAD-binding domain of type II 3 beta-HSD.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of congenital adrenal hyperplasia in two siblings with classical nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital adrenal hyperplasia due to point mutations in the type II 3 beta-hydroxysteroid dehydrogenase gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pubertal Presentation of Congenital Δ5–-3β–Hydroxysteroid Dehydrogenase Deficiency*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in the human gene for 3 beta-hydroxysteroid dehydrogenase type II leading to male pseudohermaphroditism without salt loss
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Persistent testicular delta5-isomerase-3beta-hydroxysteroid dehydrogenase (delta5-3beta-HSD) deficiency in the delta5-3beta-HSD form of congenital adrenal hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hormone synthesis and release from human fetal adenohypophyses in vitro.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of congenital adrenal hyperplasia due to 3 beta- hydroxysteroid dehydrogenase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
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%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cyproterone acetate versus hydrocortisone treatment in late-onset adrenal hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is salt-wasting in congenital adrenal hyperplasia due to the same gene as the fasciculata defect?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular analysis of type II 3 beta-hydroxysteroid dehydrogenase gene in Japanese patients with classical 3 beta-hydroxysteroid dehydrogenase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic defects of steroidogenesis in premature pubarche
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of early prenatal dexamethasone on the cognitive and behavioral development of young children: results of a pilot study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular approaches for the diagnosis of 21-hydroxylase deficiency and congenital adrenal hyperplasia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
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Steroid 21-hydroxylase deficiency: two additional mutations in salt-wasting disease and rapid screening of disease-causing mutations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
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inferred from DOI database lookup
Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
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Early diagnosis of congenital adrenal hyperplasia by measurement of 17-hydroxyprogesterone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
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3β-Hydroxysteroid Dehydrogenase Deficiency Follow-Up Study in a Girl with Pubertal Bone Age
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of nonclassical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: a small sample study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970285-1
retrieved
7 January 2021
based on heuristic
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Identifiers
DOI
10.1016/S0889-8529(05)70285-1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9429863
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429863%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PubMed publication ID
9429863
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9429863
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429863%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
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