Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis

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Bibliografiske detaljer
Main Authors:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
Format:	Journal article
Udgivet:	1998

Lignende værker

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.
af: Bastin, J, et al.
Udgivet: (1998)

HFE-Associated Hereditary Haemochromatosis
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Identification of new ligands for the haemochromatosis protein HFE
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Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload.
af: Townsend, A, et al.
Udgivet: (2002)

Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload
af: Townsend, A, et al.
Udgivet: (2002)

Clinical haemochromatosis in HFE mutation carriers.
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Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis
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Factors influencing disease phenotype and penetrance in HFE haemochromatosis.
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Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
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Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience
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Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis.
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RECRUITMENT OF PATIENTS WITH HEREDITARY HAEMOCHROMATOSIS AS BLOOD DONORS
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Hereditary haemochromatosis, haemophagocytic lymphohistiocytosis and COVID-19
af: Matthew J. Riley, et al.
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Penetrancia familiar del gen HFE: los cuatro hermanos de una familia afectados por hemocromatosis hereditaria Familiar penetrancy of HFE gene: four brothers of the same family affected by hereditary haemochromatosis
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The hemochromatosis protein HFE inhibits iron export from macrophages.
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Public health aspects of genetic screening for hereditary haemochromatosis in Australia
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The development of polycythemia vera after phlebotomy treatment for hereditary haemochromatosis
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Genetic mutations, diagnostic methods, and therapies related to hereditary haemochromatosis
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HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank
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In vitro binding of HFE to the cation-independent mannose-6 phosphate receptor.
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Ultrasound verified inflammation and structural damage in patients with hereditary haemochromatosis-related arthropathy
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Primary Biliary Cirrhosis-Specific Antimitochondrial Antibodies in Neonatal Haemochromatosis
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Inflammation can increase hepcidin in HFE‐hereditary hemochromatosis
af: Wenke Moris, et al.
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Hereditary haemochromatosis: pilot study of case-finding approach to early diagnosis in primary care.
af: Emery, J, et al.
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Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.
af: Robson, K, et al.
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Infertility: Consider haemochromatosis?
af: Lok, C, et al.
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The structure and function of HFE.
af: Drakesmith, H, et al.
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Pilot study of early diagnosis of hereditary haemochromatosis through systematic case finding in primary care.
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Pathogenesis Diagnostics and Treatment of Hereditary Haemochromatosis: A 150 Year-Long Understanding of an Iron Overload Disorder
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Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis
af: Wei Zhang, et al.
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Hereditary Hemochromatosis <it>(HFE) </it>genotypes in heart failure: Relation to etiology and prognosis
af: Torp-Pedersen Christian, et al.
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JUVENILE HAEMOCHROMATOSIS MUTATIONS ARE NOT THAT SIMPLE
af: Bignell, P, et al.
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Juvenile haemochromatosis in the Bangladeshi community
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Therapeutic monoclonal antibodies with a focus on hereditary angioedema
af: Bruce L. Zuraw, et al.
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Clinical applications of monoclonal antibodies.
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Udgivet: (1980)

Erratum: Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease and secondary iron overload (Lancet (March 2) (786))
af: Townsend, A, et al.
Udgivet: (2002)

Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease, and secondary iron overload (vol 359, pg 786, 2002)
af: Townsend, A, et al.
Udgivet: (2002)

Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation
af: J Bryant, et al.
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Screening for hereditary haemochromatosis in patients undergoing knee arthroplasty: a retrospective cohort study of 2,035 patients
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