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Proton pump inhibitors suppress absorption of dietary non-haem iron in hereditary haemochromatosis

Gut, 2007-09, Vol.56 (9), p.1291-1295

2007

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An Iron-Regulated Ferric Reductase Associated with the Absorption of Dietary Iron

Science (American Association for the Advancement of Science), 2001-03, Vol.291 (5509), p.1755-1759

2001

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iron-chelating potential of silybin in patients with hereditary haemochromatosis

European journal of clinical nutrition, 2010-10, Vol.64 (10), p.1239-1241

2010

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CD44 as a Potential Screening Marker for Preliminary Differentiation Between Congenital Dyserythropoietic Anemia Type II and Hereditary Spherocytosis

Cytometry. Part B, Clinical cytometry, 2018-03, Vol.94 (2), p.312-326

2018

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Genetics of haemochromatosis

The Lancet (British edition), 2002-11, Vol.360 (9346), p.1673-1681

Bomford, Adrian

2002

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p53 mutations in British patients with hepatocellular carcinoma: Clustering in genetic hemochromatosis

Gastroenterology (New York, N.Y. 1943), 1999-07, Vol.117 (1), p.154-160

1999

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Non-transferrin-bound iron in plasma or serum from patients with idiopathic hemochromatosis. Characterization by high performance liquid chromatography and nuclear magnetic resonance spectroscopy

The Journal of biological chemistry, 1989-03, Vol.264 (8), p.4417

1989

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Antioxidants versus corticosteroids in the treatment of severe alcoholic hepatitis—A randomised clinical trial

Journal of hepatology, 2006-04, Vol.44 (4), p.784-790

2006

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Hepatic and extrahepatic hepatitis C virus replication in relation to response to interferon therapy

Hepatology (Baltimore, Md.), 1994-12, Vol.20 (6), p.1399-1404

1994

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A Novel Duodenal Iron-Regulated Transporter, IREG1, Implicated in the Basolateral Transfer of Iron to the Circulation

Molecular cell, 2000-02, Vol.5 (2), p.299-309

2000

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Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis

Human molecular genetics, 2003-09, Vol.12 (17), p.2241-2247

2003

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The iron-chelating potential of silybin in patients with hereditary hemochromatosis

European journal of clinical nutrition, 2010-10, Vol.64 (10), p.1239

2010

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PTH-110 Long term survival following treatment for hepatocellular carcinoma in patients with hereditary haemochromatosis

Gut, 2015-06, Vol.64 (Suppl 1), p.A456-A456

2015

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Quantification of hepcidin using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

Rapid communications in mass spectrometry, 2009-06, Vol.23 (11), p.1531-1542

2009

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Hepatic expression of hepatocyte growth factor gene mRNA in acute liver failure

Digestive diseases and sciences, 2000-10, Vol.45 (10), p.1913-1920

2000

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Ferritin iron kinetics and protein turnover in K562 cells

The Journal of biological chemistry, 1988-12, Vol.263 (35), p.19181-19187

1988

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Atypical haemochromatosis: phenotypic spectrum and β2-microglobulin candidate gene analysis

Journal of medical genetics, 1999-07, Vol.36 (7), p.537-541

1999

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Differential expression of transferrin receptor in duodenal mucosa in iron overload: Evidence for a site-specific defect in genetic hemochromatosis

Gastroenterology (New York, N.Y. 1943), 1990-04, Vol.98 (4), p.976-984

1990

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H63D is an haemochromatosis associated allele

Gut, 1998-09, Vol.43 (3), p.441-441

1998

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Determinants of the interaction between the iron-responsive element-binding protein and its binding site in rat L-ferritin mRNA

The Journal of biological chemistry, 1990-04, Vol.265 (12), p.7000-7008

1990

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The effect of the iron saturation of transferrin on its binding and uptake by rabbit reticulocytes

Biochemical journal, 1984-04, Vol.219 (2), p.505-510

1984

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Reversibility of hypogonadotrophic hypogonadism associated with genetic haemochromatosis

Clinical endocrinology (Oxford), 1993-06, Vol.38 (6), p.617-620

1993

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Transferrin and its receptor: Their roles in cell function

Hepatology (Baltimore, Md.), 1985-09, Vol.5 (5), p.870-875

1985

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A duodenal mucosal abnormality in the reduction of Fe(III) in patients with genetic haemochromatosis

Gut, 1996-05, Vol.38 (5), p.765-769

1996

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Bleomycin-detectable iron in serum from leukaemic patients before and after chemotherapy Therapeutic implications for treatment with oxidant-generating drugs

FEBS letters, 1988-12, Vol.241 (1), p.202-204

1988

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Proton pump inhibitors suppress absorption of dietary non-haem iron in hereditary haemochromatosis

An Iron-Regulated Ferric Reductase Associated with the Absorption of Dietary Iron

iron-chelating potential of silybin in patients with hereditary haemochromatosis

CD44 as a Potential Screening Marker for Preliminary Differentiation Between Congenital Dyserythropoietic Anemia Type II and Hereditary Spherocytosis

Genetics of haemochromatosis

p53 mutations in British patients with hepatocellular carcinoma: Clustering in genetic hemochromatosis

Non-transferrin-bound iron in plasma or serum from patients with idiopathic hemochromatosis. Characterization by high performance liquid chromatography and nuclear magnetic resonance spectroscopy

Antioxidants versus corticosteroids in the treatment of severe alcoholic hepatitis—A randomised clinical trial

Hepatic and extrahepatic hepatitis C virus replication in relation to response to interferon therapy

A Novel Duodenal Iron-Regulated Transporter, IREG1, Implicated in the Basolateral Transfer of Iron to the Circulation

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis

The iron-chelating potential of silybin in patients with hereditary hemochromatosis

PTH-110 Long term survival following treatment for hepatocellular carcinoma in patients with hereditary haemochromatosis

Quantification of hepcidin using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

Hepatic expression of hepatocyte growth factor gene mRNA in acute liver failure

Ferritin iron kinetics and protein turnover in K562 cells

Atypical haemochromatosis: phenotypic spectrum and β2-microglobulin candidate gene analysis

Differential expression of transferrin receptor in duodenal mucosa in iron overload: Evidence for a site-specific defect in genetic hemochromatosis

H63D is an haemochromatosis associated allele

Determinants of the interaction between the iron-responsive element-binding protein and its binding site in rat L-ferritin mRNA

The effect of the iron saturation of transferrin on its binding and uptake by rabbit reticulocytes

Reversibility of hypogonadotrophic hypogonadism associated with genetic haemochromatosis

Transferrin and its receptor: Their roles in cell function

A duodenal mucosal abnormality in the reduction of Fe(III) in patients with genetic haemochromatosis

Bleomycin-detectable iron in serum from leukaemic patients before and after chemotherapy Therapeutic implications for treatment with oxidant-generating drugs

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