(Q24799152)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

title

HFE C282Y and H63D in adults with malignancies in a community medical oncology practice (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

author name string

Luigi F Bertoli

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Ronald T Acton

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

language of work or name

English

0 references

publication date

10 February 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

volume

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

issue

1

0 references

page(s)

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

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

25 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Hemochromatosis gene in leukemia and lymphoma

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Increased p53 mutation load in nontumorous human liver of wilson disease and hemochromatosis: oxyradical overload diseases

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Geography of HFE C282Y and H63D mutations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

On estimating the relation between blood group and disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Human leukocyte antigen class I and II alleles and risk of cervical neoplasia: results from a population-based study in Costa Rica.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Increased cancer risk in a cohort of 230 patients with hereditary hemochromatosis in comparison to matched control patients with non-iron-related chronic liver 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=356917

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Cohort study of internal malignancy in genetic hemochromatosis and other chronic nonalcoholic liver diseases

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Long term results of venesection therapy in idiopathic haemochromatosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Body iron stores and the risk of cancer

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Genetic analysis of multiply-affected families of insulin-dependent diabetes mellitus (IDDM) probands

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Long-term survival analysis in hereditary hemochromatosis

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Effect of erythrocytes on alveolar macrophage cytostatic activity induced by bleomycin lung damage in rats

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

High frequency of the H63D mutation of the hemochromatosis gene (HFE) in malignant gliomas.

30 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Gluconate metabolism of Pasteurellapestis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Association between hemochromatosis (HFE) gene mutation carrier status and the risk of colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Cancer risk following primary hemochromatosis: a population-based cohort study in Denmark.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Iron inhibits the nonspecific tumoricidal activity of macrophages. A possible contributory mechanism for neoplasia in hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Management of Hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Association of mutations in the hemochromatosis gene with shorter life expectancy

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Prevalence of heterozygotes for hemochromatosis in the white population of the United States.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356917

Body iron stores and risk of cancer

28 November 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Moderate elevation of body iron level and increased risk of cancer occurrence and death

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Interaction between haemochromatosis and transferrin receptor genes in different neoplastic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Iron overload in patients with sideroblastic anaemia is not related to the presence of the haemochromatosis Cys282Tyr and His63Asp mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Prevalence of hemochromatosis related HFE gene mutations in patients with acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

No evidence of increased risk of colorectal cancer in individuals heterozygous for the Cys282Tyr haemochromatosis mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

The C282Y mutation does not shorten life span

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Interaction between haemochromatosis and transferrin receptor genes in multiple myeloma

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

The frequency of the haemochromatosis C282Y mutation in the ethnic Hungarian and Romany populations of eastern Hungary

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

HFE mutations do not account for transfusional iron overload in patients with acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

High Incidence of Extrahepatic Carcinomas in Idiopathic Hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Diagnosis of hemochromatosis probands in a community hospital

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Survival and prognostic factors in 212 Italian patients with genetic hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Increased incidence of HFE C282Y mutations in patients with iron overload and hepatocellular carcinoma developed in non-cirrhotic liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Mutations of the HFE gene and the risk of hepatocellular carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Transferrin saturation phenotype and HFE genotype screening for hemochromatosis and primary iron overload: predictions from a model based on national, racial, and ethnic group composition in central Alabama

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Risk of neoplastic and other diseases among people with heterozygosity for hereditary hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Overexpression of hemochromatosis protein, HFE, alters transferrin recycling process in human hepatoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-6

Cirrhotic process, liver cell carcinoma and extrahepatic malignant tumors in idiopathic haemochromatosis. Study of 71 patients treated with venesection therapy

21 January 2018

1 reference

12 December 2020

Prevalence of HFE genotypes, C282Y and H63D, in patients with hematologic disorders

1 reference

12 December 2020

Transfusion iron overload in adults with acute leukemia: manifestations and therapy

1 reference

12 December 2020

[A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis]

1 reference

12 December 2020

Unravelling an HLA-DR association in childhood acute lymphoblastic leukemia

1 reference

12 December 2020

Hepatic pathology in relatives of patients with hæmochromatosis

1 reference

12 December 2020

The C282Y mutation of HFE is another male-specific risk factor for childhood acute lymphoblastic leukemia

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2407-4-6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

25 December 2019

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15018631%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

PubMed publication ID

15018631

1 reference