(Q42708636)

5 November 2017

0 references

Novel observations in hereditary hemochromatosis: potential implications for clinical strategies (English)

1 reference

5 November 2017

Dorine W Swinkels

1

1 reference

PMC publication ID

3069220

5 November 2017

Robert E Fleming

series ordinal

2

1 reference

5 November 2017

1 April 2011

1 reference

5 November 2017

1 reference

5 November 2017

96

1 reference

5 November 2017

4

1 reference

5 November 2017

485-488

1 reference

Mass spectrometry analysis of hepcidin peptides in experimental mouse models

5 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Novel genomic techniques open new avenues in the analysis of monogenic disorders

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Diagnosis and management of hereditary haemochromatosis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variants.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

A time course of hepcidin response to iron challenge in patients with HFE and TFR2 hemochromatosis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Two to tango: regulation of Mammalian iron metabolism

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Non-invasive assessment of tissue iron overload

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Results of the first international round robin for the quantification of urinary and plasma hepcidin assays: need for standardization

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Regulation of hepcidin and iron-overload disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Hereditary hemochromatosis: genetic complexity and new diagnostic approaches

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

EASL clinical practice guidelines for HFE hemochromatosis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Plasma hepcidin concentrations significantly predict interindividual variation in iron absorption in healthy men.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Hepcidin is decreased in TFR2 hemochromatosis

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Blunted hepcidin response to oral iron challenge in HFE-related hemochromatosis

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3069220

Synopsis of the Dutch multidisciplinary guideline for the diagnosis and treatment of hereditary haemochromatosis

30 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21454877

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Serum hepcidin levels are innately low in HFE-related haemochromatosis but differ between C282Y-homozygotes with elevated and normal ferritin levels

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21454877

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3324/HAEMATOL.2011.042036

1 reference

5 November 2017

1 reference

PMC publication ID

3069220

5 November 2017

PubMed publication ID

21454877

1 reference

PMC publication ID

3069220