(Q37694035)

English

Prevalence of nonclassic congenital adrenal hyperplasia in Turkish children presenting with premature pubarche, hirsutism, or oligomenorrhoea.

scientific article published on 23 March 2014

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24778650%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

Prevalence of nonclassic congenital adrenal hyperplasia in Turkish children presenting with premature pubarche, hirsutism, or oligomenorrhoea (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24778650%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

congenital disorder

0 references

congenital adrenal hyperplasia

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

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16 March 2020

4

1 reference

Europe PubMed Central

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16 March 2020

6

1 reference

Europe PubMed Central

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16 March 2020

author name string

Enver Simsek

2

1 reference

Europe PubMed Central

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16 March 2020

Oguz Cilingir

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24778650%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

Ozden Kutlay

5

1 reference

Europe PubMed Central

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16 March 2020

publication date

23 March 2014

1 reference

Europe PubMed Central

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16 March 2020

International journal of endocrinology

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24778650%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

2014

1 reference

Europe PubMed Central

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16 March 2020

768506

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24778650%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

copyright license

Creative Commons Attribution 3.0 Unported

1 January 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

CYP21A2 gene mutations in congenital adrenal hyperplasia: genotype-phenotype correlation in Turkish children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 August 2017

Nonclassic congenital adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 August 2017

Nonclassic adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 August 2017

Precocious pubarche in girls and the development of androgen excess

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 August 2017

Idiopathic hirsutism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 August 2017

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 August 2017

Variations in pattern of pubertal changes in girls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 August 2017

R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 August 2017

Non-classic adrenal hyperplasia due to the deficiency of 21-hydroxylase and its relation to polycystic ovarian syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

6 September 2017

Clinical presentation of children with premature adrenarche

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

6 September 2017

Hirsutism: implications, etiology, and management

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

6 September 2017

Premature pubarche: etiological heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

6 September 2017

Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

14 September 2017

The phenotype of hirsute women: a comparison of polycystic ovary syndrome and 21-hydroxylase-deficient nonclassic adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 June 2018

Prevalence of nonclassic adrenal hyperplasia (NCAH) in hyperandrogenic women

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 June 2018

The prevalence of late onset congenital adrenal hyperplasia in hirsute women from Central Anatolia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 June 2018

A practical classification of newborn infants by weight and gestational age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 June 2018

Absence of nonclassical congenital adrenal hyperplasia in patients with precocious adrenarche

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

23 June 2018

The prevalence of non-classic adrenal hyperplasia among Turkish women with hyperandrogenism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

1 September 2018

Precocious pubarche: distinguishing late-onset congenital adrenal hyperplasia from premature adrenarche.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

1 September 2018

Anthropometric and endocrine features in girls with isolated premature pubarche or non-classical congenital adrenal hyperplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

1 September 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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3981121

1 September 2018

Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F768506

21 January 2018

CYP21A2 Genotypes do not Predict the Severity of Hyperandrogenic Manifestations in the Nonclassical Form of Congenital Adrenal Hyperplasia

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F768506

21 January 2018

A multicenter study of women with nonclassical congenital adrenal hyperplasia: relationship between genotype and phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is heterozygosity for the steroid 21-hydroxylase deficiency responsible for hirsutism, premature pubarche, early puberty, and precocious puberty in children?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype-phenotype analysis in late onset 21-hydroxylase deficiency in comparison to the classical forms

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Usefulness of an ACTH Test in the Diagnosis of Nonclassical 21-Hydroxylase Deficiency among Children Presenting with Premature Pubarche

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence of non-classical 21-hydroxylase deficiency in hirsute adolescent girls

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Endocrine profile and phenotype-genotype correlation in unrelated patients with non-classical congenital adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High incidence of molecular defects of the CYP21 gene in patients with premature adrenarche

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is basal serum 17-OH progesterone a reliable parameter to predict nonclassical congenital adrenal hyperplasia in premature adrenarche?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pro-453 to Ser mutation in CYP21 is associated with nonclassic steroid 21-hydroxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V2811 mutation in patients with premature pubarche

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth references for Turkish children aged 6 to 18 years

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Body mass index references for Turkish children

1 reference

https://pubmed.ncbi.nlm.nih.gov/24778650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1155/2014/768506

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24778650%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24778650%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24778650%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

ResearchGate publication ID

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