(Q35180492)

7 August 2017

Long-term outcome of loss-of-function mutations in thyrotropin receptor gene (English)

1 reference

7 August 2017

Yardena Tenenbaum-Rakover

1

1 reference

7 August 2017

Shlomo Almashanu

2

1 reference

7 August 2017

Ora Hess

3

1 reference

7 August 2017

Osnat Admoni

4

1 reference

7 August 2017

Ahmad Hag-Dahood Mahameed

5

1 reference

7 August 2017

Naama Schwartz

6

1 reference

7 August 2017

Stavit Allon-Shalev

7

1 reference

7 August 2017

Dani Bercovich

8

1 reference

7 August 2017

Samuell Refetoff

9

1 reference

7 August 2017

28 January 2015

1 reference

7 August 2017

1 reference

7 August 2017

25

1 reference

7 August 2017

3

1 reference

7 August 2017

292-299

1 reference

Management of subclinical hypothyroidism: the thyroidologists' view

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Current loss-of-function mutations in the thyrotropin receptor gene: when to investigate, clinical effects, and treatment

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Genetic defects, thyroid growth and malfunctions of the TSHR in pediatric patients

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Loss-of-function mutations in the thyrotropin receptor gene as a major determinant of hyperthyrotropinemia in a consanguineous community

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

The clinical significance of subclinical thyroid dysfunction

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

The natural history of euthyroid Hashimoto's thyroiditis in children

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Low prevalence of thyrotropin receptor mutations in a large series of subjects with sporadic and familial nonautoimmune subclinical hypothyroidism.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Subclinical thyroid disease: scientific review and guidelines for diagnosis and management

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Resistance to thyrotropin

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Epidemiology and prevention of clinical and subclinical hypothyroidism

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Brief report: resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Longitudinal evaluation of patients with a homozygous R450H mutation of the TSH receptor gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Goitrous autoimmune thyroiditis in a pediatric population: a longitudinal study

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Continuous age-dependent reference ranges for thyroid hormones in neonates, infants, children and adolescents established using the ADVIA Centaur Analyzer

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4361004

The W546X mutation of the thyrotropin receptor gene: potential major contributor to thyroid dysfunction in a Caucasian population

27 September 2018

1 reference

12 December 2020

TSHR mutations as a cause of congenital hypothyroidism in Japan: a population-based genetic epidemiology study

1 reference

12 December 2020

Four families with loss of function mutations of the thyrotropin receptor

1 reference

12 December 2020

Natural course of 'subclinical' hypothyroidism in childhood and adolescence

1 reference

12 December 2020

Identifiers

DOI

10.1089/THY.2014.0311

1 reference

7 August 2017

1 reference

7 August 2017

1 reference