(Q34444319)

2 August 2017

1 reference

title

Congenital adrenal hyperplasia: transition from chil dhood to adulthood (English)

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congenital adrenal hyperplasia

2 August 2017

0 references

1 reference

Speiser PW

1

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2 August 2017

publication date

1 October 2001

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Journal of Endocrinological Investigation

2 August 2017

published in

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2 August 2017

volume

24

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2 August 2017

issue

9

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2 August 2017

page(s)

681-691

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Height outcome in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency: a meta-analysis

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Endocrinology and auxology of sibships with non-classical congenital adrenal hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Sexual behavior in adolescent and adult females with congenital adrenal hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Gender change from female to male in classical congenital adrenal hyperplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Cognitive function in congenital adrenal hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Hyperinsulinemia in polycystic ovary syndrome correlates with increased cardiovascular risk independent of obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Hyperinsulinaemia, dyslipaemia and cardiovascular risk in girls with a history of premature pubarche.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Adult Height and Fertility in Men with Congenital Virilizing Adrenal Hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Testicular adrenal-like tissue (TALT) in congenital adrenal hyperplasia: detection by ultrasonography

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Benign testicular tumors in children with congenital adrenal hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

The adrenal incidentaloma. A pediatric perspective

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Pregnancy outcomes in women with congenital virilizing adrenal hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

How safe is long-term prenatal glucocorticoid treatment?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Prenatal treatment of congenital adrenal hyperplasia. The United States experience

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Corticosteroid therapy in severe illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

The Interrelationship of Sodium Balance, Plasma Renin Activity and ACTH in Congenital Adrenal Hyperplasias

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Assignment of sex in neonates with ambiguous genitalia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Surgical treatment of congenital adrenal hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Characterization of single-nucleotide polymorphisms in coding regions of human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Aberrant splicing and missense mutations cause steroid 21-hydroxylase [P-450(C21)] deficiency in humans: possible gene conversion products

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

21-Hydroxylase–deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343913

Testicular adrenal rest tissue in congenital adrenal hyperplasia: serial sonographic and clinical findings

21 January 2018

1 reference

12 December 2020

Nipple differentiation in fetal male rats treated with an inhibitor of the enzyme 5 alpha-reductase: definition of a selective role for dihydrotestosterone

1 reference

12 December 2020

Behavioral effects of prenatal versus postnatal androgen excess in children with 21-hydroxylase-deficient congenital adrenal hyperplasia

1 reference

12 December 2020

Adrenal incidentaloma and patients with homozygous or heterozygous congenital adrenal hyperplasia

1 reference

12 December 2020

Estimation of daily cortisol production and clearance rates in normal pubertal males by deconvolution analysis

1 reference

12 December 2020

Male infertility due to congenital adrenal hyperplasia: testicular biopsy findings, hormonal evaluation, and therapeutic results in three patients

1 reference

12 December 2020

Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virus

1 reference

12 December 2020

Testicular masses in association with adrenogenital syndrome: US findings

1 reference

12 December 2020

Early growth is not increased in untreated moderately severe 21-hydroxylase deficiency

1 reference

12 December 2020

Virilizing adrenocortical carcinoma. Development in a patient with salt-losing congenital adrenal hyperplasia

1 reference

12 December 2020

Optimizing the diagnostic criteria for standard (250-microg) and low dose (1-microg) adrenocorticotropin tests in the assessment of adrenal function

1 reference

12 December 2020

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

1 reference

12 December 2020

High frequency of nonclassical steroid 21-hydroxylase deficiency

1 reference

12 December 2020

Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiency

1 reference

12 December 2020

The use of adrenalectomy as a treatment for congenital adrenal hyperplasia

1 reference

12 December 2020

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

1 reference

12 December 2020

Normal female infants born of mothers with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

12 December 2020

Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia

1 reference

12 December 2020

Steroid 21-hydroxylase deficiency: genotype may not predict phenotype

1 reference

12 December 2020

A polymorphism in the glucocorticoid receptor gene may be associated with and increased sensitivity to glucocorticoids in vivo.

1 reference

12 December 2020

Congenital adrenal hyperplasia presenting as massive adrenal incidentalomas in the sixth decade of life: report of two patients with 21-hydroxylase deficiency.

1 reference

12 December 2020

Identification of heterozygotic carriers of 21-hydroxylase deficiency: sensitivity of ACTH stimulation tests

1 reference

12 December 2020

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

1 reference

12 December 2020

Home monitoring of 17 hydroxyprogesterone levels in congenitx127drenal hyperplasia with filter paper blood samples

1 reference

12 December 2020

Population-wide evaluation of disease manifestation in relation to molecular genotype in steroid 21-hydroxylase (CYP21) deficiency: good correlation in a well defined population

1 reference

12 December 2020

Growth and final height in classical and nonclassical 21-hydroxylase deficiency

1 reference

12 December 2020

Ovarian hyperandrogynism as a result of congenital adrenal virilizing disorders: evidence for perinatal masculinization of neuroendocrine function in women

1 reference

12 December 2020

The quality of life in adult female patients with congenital adrenal hyperplasia: a comprehensive study of the impact of genital malformations and chronic disease on female patients life

1 reference

12 December 2020

Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees

1 reference

12 December 2020

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

12 December 2020

Testis sparing surgery for steroid unresponsive testicular tumors of the adrenogenital syndrome

1 reference

12 December 2020

Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation

1 reference

12 December 2020

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

1 reference

12 December 2020

Adrenomedullary dysplasia and hypofunction in patients with classic 21-hydroxylase deficiency

1 reference

12 December 2020

An improved method for the detection of heterozygosity of congenital virilizing adrenal hyperplasia

1 reference

12 December 2020

Clinical utility of adrenal ultrasonography in the diagnosis of congenital adrenal hyperplasia

1 reference

12 December 2020

Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1

1 reference

12 December 2020

Flutamide, testolactone, and reduced hydrocortisone dose maintain normal growth velocity and bone maturation despite elevated androgen levels in children with congenital adrenal hyperplasia.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03343913

1 reference

Dimensions Publication ID

2 August 2017

1002740791

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1 reference