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

ग्रंथसूची विवरण
मुख्य लेखकों:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
स्वरूप:	Journal article
प्रकाशित:	1998

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.
द्वारा: Bastin, J, और अन्य
प्रकाशित: (1998)

HFE-Associated Hereditary Haemochromatosis
द्वारा: Emmeke J Eijkelkamp, और अन्य
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Identification of new ligands for the haemochromatosis protein HFE
द्वारा: Drakesmith, H, और अन्य
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Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload.
द्वारा: Townsend, A, और अन्य
प्रकाशित: (2002)

Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload
द्वारा: Townsend, A, और अन्य
प्रकाशित: (2002)

Clinical haemochromatosis in HFE mutation carriers.
द्वारा: Cox, T, और अन्य
प्रकाशित: (2002)

Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis
द्वारा: Barton David E, और अन्य
प्रकाशित: (2006-11-01)

Factors influencing disease phenotype and penetrance in HFE haemochromatosis.
द्वारा: Rochette, J, और अन्य
प्रकाशित: (2010)

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
द्वारा: Merryweather-Clarke, A, और अन्य
प्रकाशित: (2003)

Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience
द्वारा: Robson, K, और अन्य
प्रकाशित: (2000)

Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis.
द्वारा: Sebastiani, G, और अन्य
प्रकाशित: (2003)

RECRUITMENT OF PATIENTS WITH HEREDITARY HAEMOCHROMATOSIS AS BLOOD DONORS
द्वारा: Marko Cukjati, और अन्य
प्रकाशित: (2004-12-01)

Hereditary haemochromatosis, haemophagocytic lymphohistiocytosis and COVID-19
द्वारा: Matthew J. Riley, और अन्य
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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
द्वारा: M. Vázquez Romero, और अन्य
प्रकाशित: (2005-08-01)

The hemochromatosis protein HFE inhibits iron export from macrophages.
द्वारा: Drakesmith, H, और अन्य
प्रकाशित: (2002)

Public health aspects of genetic screening for hereditary haemochromatosis in Australia
द्वारा: Dorota M. Gertig, और अन्य
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The development of polycythemia vera after phlebotomy treatment for hereditary haemochromatosis
द्वारा: Erik JM vanBommel, और अन्य
प्रकाशित: (2021-08-01)

Genetic mutations, diagnostic methods, and therapies related to hereditary haemochromatosis
द्वारा: Karina Marini Aguiar, और अन्य
प्रकाशित: (2014-03-01)

HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank
द्वारा: Luke C Pilling, और अन्य
प्रकाशित: (2024-03-01)

In vitro binding of HFE to the cation-independent mannose-6 phosphate receptor.
द्वारा: Schimanski, L, और अन्य
प्रकाशित: (2009)

Ultrasound verified inflammation and structural damage in patients with hereditary haemochromatosis-related arthropathy
द्वारा: Christian Dejaco, और अन्य
प्रकाशित: (2017-10-01)

Primary Biliary Cirrhosis-Specific Antimitochondrial Antibodies in Neonatal Haemochromatosis
द्वारा: Daniel S. Smyk, और अन्य
प्रकाशित: (2013-01-01)

Inflammation can increase hepcidin in HFE‐hereditary hemochromatosis
द्वारा: Wenke Moris, और अन्य
प्रकाशित: (2021-05-01)

Hereditary haemochromatosis: pilot study of case-finding approach to early diagnosis in primary care.
द्वारा: Emery, J, और अन्य
प्रकाशित: (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.
द्वारा: Robson, K, और अन्य
प्रकाशित: (2004)

Infertility: Consider haemochromatosis?
द्वारा: Lok, C, और अन्य
प्रकाशित: (2007)

The molecular genetics of haemochromatosis
द्वारा: Shearman, J, और अन्य
प्रकाशित: (1996)

The structure and function of HFE.
द्वारा: Drakesmith, H, और अन्य
प्रकाशित: (2000)

Pilot study of early diagnosis of hereditary haemochromatosis through systematic case finding in primary care.
द्वारा: Emery, J, और अन्य
प्रकाशित: (2002)

Pathogenesis Diagnostics and Treatment of Hereditary Haemochromatosis: A 150 Year-Long Understanding of an Iron Overload Disorder
द्वारा: Anastasia Asimakopoulou, और अन्य
प्रकाशित: (2017-11-01)

Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis
द्वारा: Wei Zhang, और अन्य
प्रकाशित: (2022-06-01)

Hereditary Hemochromatosis <it>(HFE) </it>genotypes in heart failure: Relation to etiology and prognosis
द्वारा: Torp-Pedersen Christian, और अन्य
प्रकाशित: (2010-07-01)

JUVENILE HAEMOCHROMATOSIS MUTATIONS ARE NOT THAT SIMPLE
द्वारा: Bignell, P, और अन्य
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Juvenile haemochromatosis in the Bangladeshi community
द्वारा: Lok, C, और अन्य
प्रकाशित: (2007)

Therapeutic monoclonal antibodies with a focus on hereditary angioedema
द्वारा: Bruce L. Zuraw, और अन्य
प्रकाशित: (2023-01-01)

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द्वारा: Mcmichael, A, और अन्य
प्रकाशित: (1980)

Erratum: Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease and secondary iron overload (Lancet (March 2) (786))
द्वारा: Townsend, A, और अन्य
प्रकाशित: (2002)

Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease, and secondary iron overload (vol 359, pg 786, 2002)
द्वारा: Townsend, A, और अन्य
प्रकाशित: (2002)

Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation
द्वारा: J Bryant, और अन्य
प्रकाशित: (2009-04-01)

Screening for hereditary haemochromatosis in patients undergoing knee arthroplasty: a retrospective cohort study of 2,035 patients
द्वारा: Elisha Krasin, और अन्य
प्रकाशित: (2021-12-01)

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

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