(Q37238987)

19 August 2017

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title

Nonclassic adrenal hyperplasia. (English)

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19 August 2017

Phyllis W Speiser

1

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19 August 2017

publication date

1 March 2009

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Reviews in Endocrine and Metabolic Disorders

19 August 2017

published in

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19 August 2017

volume

10

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19 August 2017

issue

1

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19 August 2017

page(s)

77-82

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https://scigraph.springernature.com/pub.10.1007/s11154-008-9097-x

19 August 2017

exact match

0 references

cites work

Development of cortisol circadian rhythm in infancy

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12 December 2020

Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiency

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12 December 2020

Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia

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Reexamination of the age limit for defining when puberty is precocious in girls in the United States: implications for evaluation and treatment. Drug and Therapeutics and Executive Committees of the Lawson Wilkins Pediatric Endocrine Society

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12 December 2020

High frequency of nonclassical steroid 21-hydroxylase deficiency

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12 December 2020

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

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12 December 2020

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12 December 2020

Clinical practice. Hirsutism

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Isolated precocious pubarche: an approach

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12 December 2020

Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia.

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12 December 2020

Reduction of the false-positive rate in newborn screening by implementation of MS/MS-based second-tier tests: the Mayo Clinic experience (2004-2007)

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12 December 2020

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

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12 December 2020

Adrenal steroidogenesis in very low birth weight preterm infants

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12 December 2020

Reversible male infertility in late onset congenital adrenal hyperplasia

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12 December 2020

Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data*

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12 December 2020

Neonatal screening for congenital adrenal hyperplasia: 17-hydroxyprogesterone levels and CYP21 genotypes in preterm infants

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12 December 2020

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

1 reference

12 December 2020

Screening for 21-hydroxylase-deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study

1 reference

12 December 2020

Adrenarche - physiology, biochemistry and human disease

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12 December 2020

Newborn screening for congenital adrenal hyperplasia

1 reference

12 December 2020

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

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12 December 2020

Refining hormonal diagnosis of type II 3beta-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 genotyping.

1 reference

12 December 2020

Improved specificity of newborn screening for congenital adrenal hyperplasia by second-tier steroid profiling using tandem mass spectrometry

1 reference

12 December 2020

10.1007/S11154-008-9097-X

Identifiers

DOI

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19 August 2017

1 reference