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

عرض إصدارات أخرى (1)

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
التنسيق:	Journal article
منشور في:	1998

مواد مشابهة

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.
حسب: Bastin, J, وآخرون
منشور في: (1998)

HFE-Associated Hereditary Haemochromatosis
حسب: Emmeke J Eijkelkamp, وآخرون
منشور في: (2000-01-01)

Identification of new ligands for the haemochromatosis protein HFE
حسب: Drakesmith, H, وآخرون
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Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload.
حسب: Townsend, A, وآخرون
منشور في: (2002)

Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload
حسب: Townsend, A, وآخرون
منشور في: (2002)

Clinical haemochromatosis in HFE mutation carriers.
حسب: Cox, T, وآخرون
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Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis
حسب: Barton David E, وآخرون
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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.
حسب: Sebastiani, G, وآخرون
منشور في: (2003)

RECRUITMENT OF PATIENTS WITH HEREDITARY HAEMOCHROMATOSIS AS BLOOD DONORS
حسب: Marko Cukjati, وآخرون
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Hereditary haemochromatosis, haemophagocytic lymphohistiocytosis and COVID-19
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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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منشور في: (2005-08-01)

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.
حسب: Schimanski, L, وآخرون
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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
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Hereditary haemochromatosis: pilot study of case-finding approach to early diagnosis in primary care.
حسب: Emery, J, وآخرون
منشور في: (2001)

Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.
حسب: Robson, K, وآخرون
منشور في: (2004)

Infertility: Consider haemochromatosis?
حسب: Lok, C, وآخرون
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The molecular genetics of haemochromatosis
حسب: Shearman, J, وآخرون
منشور في: (1996)

The structure and function of HFE.
حسب: Drakesmith, H, وآخرون
منشور في: (2000)

Pilot study of early diagnosis of hereditary haemochromatosis through systematic case finding in primary care.
حسب: Emery, J, وآخرون
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Pathogenesis Diagnostics and Treatment of Hereditary Haemochromatosis: A 150 Year-Long Understanding of an Iron Overload Disorder
حسب: Anastasia Asimakopoulou, وآخرون
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Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis
حسب: Wei Zhang, وآخرون
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Hereditary Hemochromatosis <it>(HFE) </it>genotypes in heart failure: Relation to etiology and prognosis
حسب: Torp-Pedersen Christian, وآخرون
منشور في: (2010-07-01)

JUVENILE HAEMOCHROMATOSIS MUTATIONS ARE NOT THAT SIMPLE
حسب: Bignell, P, وآخرون
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Juvenile haemochromatosis in the Bangladeshi community
حسب: Lok, C, وآخرون
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Therapeutic monoclonal antibodies with a focus on hereditary angioedema
حسب: Bruce L. Zuraw, وآخرون
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Clinical applications of monoclonal antibodies.
حسب: Mcmichael, A, وآخرون
منشور في: (1980)

Erratum: Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease and secondary iron overload (Lancet (March 2) (786))
حسب: Townsend, A, وآخرون
منشور في: (2002)

Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease, and secondary iron overload (vol 359, pg 786, 2002)
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Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation
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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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