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Hereditary haemochromatosis: never seen a case?
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
editorial
0 references
title
Hereditary haemochromatosis: never seen a case?
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
author name string
Emery J
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Rose P
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
publication date
1 May 2001
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
published in
British Journal of General Practice
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
volume
51
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
issue
466
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
page(s)
347-348
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
cites work
Role of C282Y mutation in haemochromatosis gene in development of type 2 diabetes in healthy men: prospective cohort study
1 reference
stated in
PubMed Central
reference URL
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28 July 2018
Screening for genetic haemochromatosis in blood samples with raised alanine aminotransferase.
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PubMed Central
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28 July 2018
Hereditary haemochromatosis: to screen or not. Conditions for screening are not yet fulfilled
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1313995
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28 July 2018
The career outcomes for doctors completing general practice vocational training 1990-1995
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PubMed Central
reference URL
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28 July 2018
Population screening for hemochromatosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1313995
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28 July 2018
Is general practice in need of a career structure?
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28 July 2018
Global prevalence of putative haemochromatosis mutations
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28 July 2018
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1313995
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28 July 2018
An evaluation of the hospital component of general practice vocational training.
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PubMed Central
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28 July 2018
Long term results of venesection therapy in idiopathic haemochromatosis
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1313995
retrieved
28 July 2018
Controversy in primary care: Should asymptomatic haemochromatosis be treated?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1313995
retrieved
28 October 2018
The specialist of the discipline of general practice. Semantics and politics mustn't impede the progress of general practice
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1313995
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28 October 2018
Prevalence of hereditary hemochromatosis in 16031 primary care patients
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PubMed Central
reference URL
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28 October 2018
Genetic discrimination in life insurance: empirical evidence from a cross sectional survey of genetic support groups in the United Kingdom
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28 October 2018
Hereditary hemochromatosis: gene discovery and its implications for population-based screening
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PubMed Central
reference URL
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28 October 2018
Vocational training and beyond--listening to voices from a void
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1313995
retrieved
28 October 2018
Screening for hemochromatosis and iron deficiency in employees and primary care patients in Western Germany.
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stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1313995
retrieved
28 October 2018
Population screening for haemochromatosis: a unifying analysis of published intervention trials
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1313995
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28 October 2018
Cost-effectiveness of screening for hereditary hemochromatosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1313995
retrieved
28 October 2018
A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11360695
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
C282Y mutation in HFE (haemochromatosis) gene and type 2 diabetes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11360695
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A survey of 2,851 patients with hemochromatosis: symptoms and response to treatment
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11360695
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Increased Risk of Acute Myocardial Infarction in Carriers of the Hemochromatosis Gene Cys282Tyr Mutation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11360695
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Major determinants of consumer satisfaction with primary care in different health systems
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11360695
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Long-term survival in patients with hereditary hemochromatosis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11360695
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1313995
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
PubMed publication ID
11360695
1 reference
stated in
Europe PubMed Central
PMC publication ID
1313995
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11360695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
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