(Q42481811)

English

The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis

scientific article published on 31 August 2015

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

1 November 2017

The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis (English)

1 reference

Europe PubMed Central

1 November 2017

congenital disorder

0 references

congenital adrenal hyperplasia due to 21-hydroxylase deficiency

0 references

Alina Kuryłowicz

3

object named as

Alina Kuryłowicz

1 reference

Europe PubMed Central

1 November 2017

author name string

Urszula Ambroziak

1

1 reference

Europe PubMed Central

1 November 2017

Anna Kępczyńska-Nyk

2

1 reference

Europe PubMed Central

1 November 2017

Ewa Maria Małunowicz

4

1 reference

Europe PubMed Central

1 November 2017

Anna Wójcicka

5

1 reference

Europe PubMed Central

1 November 2017

Piotr Miśkiewicz

6

1 reference

Europe PubMed Central

1 November 2017

Magdalena Macech

7

1 reference

Europe PubMed Central

1 November 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

31 August 2015

1 reference

Europe PubMed Central

1 November 2017

Clinical Endocrinology

1 reference

Europe PubMed Central

1 November 2017

84

1 reference

Europe PubMed Central

1 November 2017

1

1 reference

Europe PubMed Central

1 November 2017

23-29

1 reference

Europe PubMed Central

1 November 2017

Diagnosis of hyperandrogenism: clinical criteria

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Polycystic Ovary Syndrome

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

A prospective study of the prevalence of nonclassical congenital adrenal hyperplasia among women presenting with hyperandrogenic symptoms and signs.

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Nonclassic 21-hydroxylase deficiency.

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Clinical assessment of body hair growth in women

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Late-onset 21-hydroxylase deficiency: reliable diagnosis by steroid analysis of random urine collections

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome (PCOS).

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Phenotypic variation in hyperandrogenic women influences the findings of abnormal metabolic and cardiovascular risk parameters

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

The prevalence, molecular analysis and HLA typing of late-onset 21-hydroxylase deficiency in Turkish woman with hirsutism and polycystic ovary

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Limited value of serum steroid measurements in identification of mild form of 21-hydroxylase deficiency.

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Steroid profiling for congenital adrenal hyperplasia by tandem mass spectrometry as a second-tier test reduces follow-up burdens in a tertiary care hospital: a retrospective and prospective evaluation

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Analysis of 17 α-hydroxyprogesterone in bloodspots by liquid chromatography tandem mass spectrometry.

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Detection of late onset steroid 21-hydroxylase deficiency by capillary gas chromatographic profiling of urinary steroids in children and adolescents.

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Detection and assignment of CYP21 mutations using peptide mass signature genotyping

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Predicting the functional effect of amino acid substitutions and indels

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

A method and server for predicting damaging missense mutations

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

The prevalence and features of the polycystic ovary syndrome in an unselected population

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12935

21 January 2018

Identifiers

10.1111/CEN.12935

1 reference

Europe PubMed Central

1 November 2017

1 reference

Europe PubMed Central

1 November 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q42481811&oldid=2091759685"