Biological variability of transferrin saturation and unsaturated iron-binding capacity. (Q36295170)

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9 January 2020

title

Biological variability of transferrin saturation and unsaturated iron-binding capacity (English)

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9 January 2020

3

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9 January 2020

author name string

Paul C Adams

1

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9 January 2020

David M Reboussin

2

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9 January 2020

James C Barton

4

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9 January 2020

Ronald T Acton

5

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9 January 2020

Godfrey C Moses

6

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9 January 2020

Catherine Leiendecker-Foster

7

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9 January 2020

Gordon D McLaren

8

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9 January 2020

Fitzroy W Dawkins

9

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9 January 2020

Victor R Gordeuk

10

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9 January 2020

Laura Lovato

11

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9 January 2020

John H Eckfeldt

12

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9 January 2020

language of work or name

English

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publication date

1 November 2007

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American Journal of Medicine

9 January 2020

published in

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volume

120

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9 January 2020

issue

11

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9 January 2020

page(s)

999.e1-7

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Screening for hereditary hemochromatosis: a systematic review for the U.S. Preventive Services Task Force

9 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

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

30 September 2017

1 reference

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Hereditary hemochromatosis--a new look at an old disease

30 September 2017

1 reference

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Insurance, employment, and psychosocial consequences of a diagnosis of hereditary hemochromatosis in subjects without end organ damage

30 September 2017

1 reference

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Nonexpressing homozygotes for C282Y hemochromatosis: minority or majority of cases?

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Twenty-four hour variation of transferrin saturation in treated and untreated haemochromatosis homozygotes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Diurnal Variations of the Serum Iron in Normal Subjects and in Patients with Haemochromatosis

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Concerns in a primary care population about genetic discrimination by insurers.

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Hemochromatosis mutations in the general population: iron overload progression rate

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Natural history of the C282Y homozygote for the hemochromatosis gene (HFE) with a normal serum ferritin level.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Psychosocial impact of C282Y mutation testing for hemochromatosis.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Diagnosis and management of hemochromatosis.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Genetic discrimination and screening for hemochromatosis: then and now.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151312

Hereditary hemochromatosis: gene discovery and its implications for population-based screening.

22 September 2018

1 reference

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Screening for hemochromatosis: high prevalence and low morbidity in an unselected population of 65,238 persons

22 September 2018

1 reference

12 December 2020

Diurnal variation of serum iron, iron-binding capacity, transferrin saturation, and ferritin levels

1 reference

12 December 2020

Circadian variations of transferrin saturation levels in iron-overloaded patients: implications for the screening of C282Y-linked haemochromatosis

1 reference

12 December 2020

Circadian rhythm of plasma iron, total iron binding capacity and serum ferritin in arteriosclerotic aged patients

1 reference

12 December 2020

Screening blood donors for hereditary hemochromatosis: decision analysis model based on a 30-year database

1 reference

12 December 2020

Management of Hemochromatosis

1 reference

12 December 2020

Diurnalnocturnal variations of certain blood constituents in normal human subjects: plasma iron, siderophilin, bilirubin, copper, total serum protein and albumin, haemoglobin and haematocrit

1 reference

12 December 2020

Comparison of the unsaturated iron-binding capacity with transferrin saturation as a screening test to detect C282Y homozygotes for hemochromatosis in 101,168 participants in the hemochromatosis and iron overload screening (HEIRS) study

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1016/J.AMJMED.2007.02.027

Identifiers

DOI

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9 January 2020

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9 January 2020

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