(Q37508836)

20 August 2017

1 reference

title

An update to 21-hydroxylase deficient congenital adrenal hyperplasia (English)

1 reference

20 August 2017

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Eftihios Trakakis

1

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20 August 2017

George Basios

2

1 reference

20 August 2017

Pantelis Trompoukis

3

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20 August 2017

George Labos

4

1 reference

20 August 2017

Ioannis Grammatikakis

5

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20 August 2017

Demetrios Kassanos

6

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20 August 2017

1 January 2010

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Gynecological Endocrinology

20 August 2017

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20 August 2017

26

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20 August 2017

1

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20 August 2017

63-71

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Androgen excess in women: experience with over 1000 consecutive patients

20 August 2017

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

21-Hydroxylase deficiency: from molecular genetics to clinical presentation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Steroidogenesis in the human skin: 21-hydroxylation in cultured keratinocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Combinatorial code of growth factors and neuropeptides define neuroendocrine differentiation in PC12 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Studies of the neuronal transdifferentiation process in cultured human pheochromocytoma cells: effects of steroids with differing functional groups on catecholamine content and cell morphology.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Glucocorticoids stimulate transcription of the rat phenylethanolamine N-methyltransferase (PNMT) gene in vivo and in vitro.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Patients with classic congenital adrenal hyperplasia have decreased epinephrine reserve and defective glucose elevation in response to high-intensity exercise

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Children with classic congenital adrenal hyperplasia have decreased amygdala volume: potential prenatal and postnatal hormonal effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Obesity among children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Extensive clinical experience: nonclassical 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Benign testicular tumors in children with congenital adrenal hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Congenital adrenal hyperplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

The incidence of 21 alpha-hydroxylase deficiency in Greek hyperandrogenic women: screening and diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

21-hydroxylase-deficient nonclassic adrenal hyperplasia: the great pretender

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Sexual function and genital sensitivity following feminizing genitoplasty for congenital adrenal hyperplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Novel mutations in CYP21 detected in individuals with hyperandrogenism.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia: implications for genetic counseling

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Prenatal diagnosis and treatment of congenital adrenal hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Cognitive functions in children at risk for congenital adrenal hyperplasia treated prenatally with dexamethasone

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Congenital adrenal hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

Presence of fetal DNA in maternal plasma and serum

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903015494

10.3109/09513590903015494

21 January 2018

Identifiers

DOI

1 reference

20 August 2017

1 reference