Influence of the A3669G Glucocorticoid Receptor Gene Polymorphism on the Metabolic Profile of Pediatric Patients with Congenital Adrenal Hyperplasia. (Q33890702)

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English	Influence of the A3669G Glucocorticoid Receptor Gene Polymorphism on the Metabolic Profile of Pediatric Patients with Congenital Adrenal Hyperplasia.	scientific article

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25050120%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

Influence of the A3669G Glucocorticoid Receptor Gene Polymorphism on the Metabolic Profile of Pediatric Patients with Congenital Adrenal Hyperplasia (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25050120%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

congenital disorder

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author name string

Ricardo P P Moreira

1

1 reference

Europe PubMed Central

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10 March 2020

Larissa G Gomes

2

1 reference

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10 March 2020

Guiomar Madureira

3

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10 March 2020

publication date

23 June 2014

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10 March 2020

International journal of endocrinology

1 reference

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10 March 2020

2014

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10 March 2020

594710

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10 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

Impact of glucocorticoid receptor gene polymorphisms on the metabolic profile of adult patients with the classical form of 21-hydroxylase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4094695

5 July 2018

Pharmacogenetics of glucocorticoid replacement could optimize the treatment of 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=4094695

5 July 2018

Health problems 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=4094695

5 July 2018

Health status of adults with congenital adrenal hyperplasia: a cohort study of 203 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4094695

5 July 2018

Congenital adrenal hyperplasia in adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4094695

5 July 2018

Clinical features associated with glucocorticoid receptor polymorphisms. An overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4094695

5 July 2018

Unfavourable trends in cardiovascular and metabolic risk in paediatric and adult patients with congenital adrenal hyperplasia?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4094695

5 July 2018

Utility of the modified ATP III defined metabolic syndrome and severe obesity as predictors of insulin resistance in overweight children and adolescents: a cross-sectional study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4094695

5 July 2018

Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4094695

5 July 2018

Family history: an opportunity for early interventions and improved control of hypertension, obesity and diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4094695

5 July 2018

Congenital adrenal hyperplasia.

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

Congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

Molecular analysis of CYP21A2 can optimize the follow-up of positive results in newborn screening for congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

Alterations in lipid and carbohydrate metabolism in patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

Children with classic congenital adrenal hyperplasia have elevated serum leptin concentrations and insulin resistance: potential clinical implications

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

Glucocorticoid receptor gene and risk of cardiovascular disease

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

Detection of the Bcl I polymorphism of the glucocorticoid receptor gene by single-tube allele-specific polymerase chain reaction.

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

Familial glucocorticoid resistance caused by a splice site deletion in the human glucocorticoid receptor gene.

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

Cardiovascular risk factors and ultrasound evaluation of intima-media thickness at common carotids, carotid bulbs, and femoral and abdominal aorta arteries in patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

Waist circumference percentiles in nationally representative samples of African-American, European-American, and Mexican-American children and adolescents

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F594710

21 January 2018

Molecular Genotyping in Brazilian Patients with the Classical and Nonclassical Forms of 21-Hydroxylase Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/25050120

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth pattern during the first 36 months of life in congenital adrenal hyperplasia (21-hydroxylase deficiency)

1 reference

https://pubmed.ncbi.nlm.nih.gov/25050120

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical pharmacology of the anti-inflammatory steroids

1 reference

https://pubmed.ncbi.nlm.nih.gov/25050120

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipid profile in congenital adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/25050120

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genes, lifestyles and obesity

1 reference

https://pubmed.ncbi.nlm.nih.gov/25050120

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1155/2014/594710

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25050120%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25050120%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25050120%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

ResearchGate publication ID

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