Thyroid-stimulating hormone and free thyroxine levels in persons with HFE C282Y homozygosity, a common hemochromatosis genotype: the HEIRS study (Q33801433)

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English	Thyroid-stimulating hormone and free thyroxine levels in persons with HFE C282Y homozygosity, a common hemochromatosis genotype: the HEIRS study	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Thyroid-stimulating hormone and free thyroxine levels in persons with HFE C282Y homozygosity, a common hemochromatosis genotype: the HEIRS study (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1 reference

based on heuristic

inferred from title

author name string

James C Barton

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Catherine Leiendecker-Foster

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

David M Reboussin

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Paul C Adams

4

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Ronald T Acton

5

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

John H Eckfeldt

6

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Hemochromatosis and Iron Overload Screening Study Research Investigators

7

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

publication date

1 August 2008

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

18

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

831-838

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

New reference intervals for thyrotropin and thyroid hormones based on National Academy of Clinical Biochemistry criteria and regular ultrasonography of the thyroid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Hemochromatosis and iron-overload screening in a racially diverse population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Establishment of a serum thyroid stimulating hormone (TSH) reference interval in healthy adults. The importance of environmental factors, including thyroid antibodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Hemochromatosis and Iron Overload Screening (HEIRS) study design for an evaluation of 100,000 primary care-based adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFE C282Y homozygosity in central Alabama.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Serum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III).

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

10 December 2018

The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Hepatic iron concentration in hereditary hemochromatosis does not saturate or accurately predict phlebotomy requirements.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Practice guideline development task force of the College of American Pathologists. Hereditary hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Hypopituitarism in primary haemochromatosis; recovery after iron depletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Pituitary function in haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Pituitary function in idiopathic haemochromatosis and cirrhosis of the liver

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Assignment of the gene for the beta subunit of thyroid-stimulating hormone to the short arm of human chromosome 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Pituitary siderosis. A histologic, immunocytologic, and ultrastructural study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

An investigation into gonadal dysfunction in patients with idiopathic haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

4 July 2018

Secondary hypothyroidism in hereditary hemochromatosis: recovery after iron depletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

30 October 2018

National Health and Nutrition Examination Survey III thyroid-stimulating hormone (TSH)-thyroperoxidase antibody relationships demonstrate that TSH upper reference limits may be skewed by occult thyroid dysfunction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

30 October 2018

Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in whites and blacks in the Hemochromatosis and Iron Overload Screening Study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

30 October 2018

Reference intervals of serum thyroid function tests in a previously iodine-deficient area

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

30 October 2018

Analysis of HLA genes in families with autoimmune diabetes and thyroiditis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

30 October 2018

Refined genotype-phenotype correlations in cases of chromosome 6p deletion syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

30 October 2018

Increased thyroid function in haemochromatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

30 October 2018

Persons with screening-detected haemochromatosis: as healthy as the general population?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

30 October 2018

Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

30 October 2018

Prevalence of hereditary hemochromatosis in 16031 primary care patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2857452

30 October 2018

Thyroid disease in hemochromatosis. Increased incidence in homozygous men.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of hemochromatosis probands in a community hospital

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA-DPB1 polymorphisms on the MHC-extended haplotypes of families of patients with Graves' disease: two distinct HLA-DR17 haplotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variable immunodeficiency and IgG subclass deficiency in central Alabama hemochromatosis probands homozygous for HFE C282Y

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haemochromatosis associated with arthritis and hypopituitarism

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemochromatosis and hemosiderosis. Study of 211 autopsied cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Gonadal and pituitary function in idiopathic hemochromatosis]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thyroid function in haemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship of body iron stores to levels of serum ferritin, serum iron, unsaturated iron binding capacity and transferrin saturation in patients with iron storage disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypogonadotropic hypogonadism in hemochromatosis: recovery of reproductive function after iron depletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome assignment of genes encoding the alpha and beta subunits of glycoprotein hormones in man and mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beware of multiple comparisons: a study of symptoms associated with mutations of the HFE hemochromatosis gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Changes in the tumor marker concentration in female patients with hyper-, eu-, and hypothyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA Associations with Hashimoto's thyroiditis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relation between thyroid status and ferritin metabolism in rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/18651828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1089/THY.2008.0091

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

ResearchGate publication ID

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