Accuracy of family history of hemochromatosis or iron overload: the hemochromatosis and iron overload screening study. (Q37187759)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18585964%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Accuracy of family history of hemochromatosis or iron overload: the hemochromatosis and iron overload screening study (English)

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9 January 2020

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2

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9 January 2020

author name string

Ronald T Acton

1

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9 January 2020

Leah V Passmore

3

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9 January 2020

Paul C Adams

4

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9 January 2020

Gordon D McLaren

5

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9 January 2020

Catherine Leiendecker-Foster

6

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9 January 2020

Mark R Speechley

7

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9 January 2020

Emily L Harris

8

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9 January 2020

Oswaldo Castro

9

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9 January 2020

Jacob A Reiss

10

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9 January 2020

Beverly M Snively

11

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9 January 2020

Barbara W Harrison

12

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9 January 2020

Christine E McLaren

13

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9 January 2020

language of work or name

English

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publication date

27 June 2008

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Clinical Gastroenterology and Hepatology

9 January 2020

published in

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9 January 2020

volume

6

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9 January 2020

issue

8

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9 January 2020

page(s)

934-938

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

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=3779058

Population screening in hereditary hemochromatosis

6 September 2017

1 reference

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Statistical tests for detection of misspecified relationships by use of genome-screen data

6 September 2017

1 reference

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PedCheck: a program for identification of genotype incompatibilities in linkage analysis

6 September 2017

1 reference

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3779058

Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3779058

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3779058

A comparison of positive family history definitions for defining risk of future disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3779058

A genome-wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3779058

Clinically overt hereditary hemochromatosis in Denmark 1948-1985: epidemiology, factors of significance for long-term survival, and causes of death in 179 patients.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3779058

Accuracy of proband reported family history: the NHLBI Family Heart Study (FHS).

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3779058

Population screening for haemochromatosis: expectations based on a study of relatives of symptomatic probands.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3779058

Risk of disease in siblings of patients with hereditary hemochromatosis

3 September 2018

1 reference

12 December 2020

A primer for predicting risk of disease in HFE-linked hemochromatosis

1 reference

12 December 2020

Acceptance of neonatal genetic screening for hereditary hemochromatosis by informed parents.

1 reference

12 December 2020

Can family history be used as a tool for public health and preventive medicine?

1 reference

12 December 2020

Survey of physician knowledge about hemochromatosis

1 reference

12 December 2020

Research priorities for evaluating family history in the prevention of common chronic diseases

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12 December 2020

Patient compliance with phlebotomy therapy for iron overload associated with hemochromatosis

1 reference

12 December 2020

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

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12 December 2020

Predictive value of family history in diagnosis of hereditary hemochromatosis

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12 December 2020

Management of Hemochromatosis

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12 December 2020

A survey of 2,851 patients with hemochromatosis: symptoms and response to treatment

1 reference

12 December 2020

Genetic susceptibility screening in schools: attitudes of the school community towards hereditary haemochromatosis

1 reference

12 December 2020

Family history of diabetes, awareness of risk factors, and health behaviors among African Americans

1 reference

12 December 2020

Hemochromatosis-associated morbidity in the United States: an analysis of the National Hospital Discharge Survey, 1979-1997

1 reference

12 December 2020

10.1016/J.CGH.2008.04.003

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18585964%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18585964%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

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