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

Show other versions (1)

Xehetasun bibliografikoak
Egile Nagusiak:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
Formatua:	Journal article
Argitaratua:	1998

Antzeko izenburuak

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

HFE-Associated Hereditary Haemochromatosis
nork: Emmeke J Eijkelkamp, et al.
Argitaratua: (2000-01-01)

Identification of new ligands for the haemochromatosis protein HFE
nork: Drakesmith, H, et al.
Argitaratua: (2007)

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

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

Clinical haemochromatosis in HFE mutation carriers.
nork: Cox, T, et al.
Argitaratua: (2002)

Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis
nork: Barton David E, et al.
Argitaratua: (2006-11-01)

Factors influencing disease phenotype and penetrance in HFE haemochromatosis.
nork: Rochette, J, et al.
Argitaratua: (2010)

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
nork: Merryweather-Clarke, A, et al.
Argitaratua: (2003)

Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience
nork: Robson, K, et al.
Argitaratua: (2000)

Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis.
nork: Sebastiani, G, et al.
Argitaratua: (2003)

RECRUITMENT OF PATIENTS WITH HEREDITARY HAEMOCHROMATOSIS AS BLOOD DONORS
nork: Marko Cukjati, et al.
Argitaratua: (2004-12-01)

Hereditary haemochromatosis, haemophagocytic lymphohistiocytosis and COVID-19
nork: Matthew J. Riley, et al.
Argitaratua: (2020-10-01)

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
nork: M. Vázquez Romero, et al.
Argitaratua: (2005-08-01)

The hemochromatosis protein HFE inhibits iron export from macrophages.
nork: Drakesmith, H, et al.
Argitaratua: (2002)

Public health aspects of genetic screening for hereditary haemochromatosis in Australia
nork: Dorota M. Gertig, et al.
Argitaratua: (2002-12-01)

The development of polycythemia vera after phlebotomy treatment for hereditary haemochromatosis
nork: Erik JM vanBommel, et al.
Argitaratua: (2021-08-01)

Genetic mutations, diagnostic methods, and therapies related to hereditary haemochromatosis
nork: Karina Marini Aguiar, et al.
Argitaratua: (2014-03-01)

HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank
nork: Luke C Pilling, et al.
Argitaratua: (2024-03-01)

In vitro binding of HFE to the cation-independent mannose-6 phosphate receptor.
nork: Schimanski, L, et al.
Argitaratua: (2009)

Ultrasound verified inflammation and structural damage in patients with hereditary haemochromatosis-related arthropathy
nork: Christian Dejaco, et al.
Argitaratua: (2017-10-01)

Primary Biliary Cirrhosis-Specific Antimitochondrial Antibodies in Neonatal Haemochromatosis
nork: Daniel S. Smyk, et al.
Argitaratua: (2013-01-01)

Inflammation can increase hepcidin in HFE‐hereditary hemochromatosis
nork: Wenke Moris, et al.
Argitaratua: (2021-05-01)

Hereditary haemochromatosis: pilot study of case-finding approach to early diagnosis in primary care.
nork: Emery, J, et al.
Argitaratua: (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.
nork: Robson, K, et al.
Argitaratua: (2004)

Infertility: Consider haemochromatosis?
nork: Lok, C, et al.
Argitaratua: (2007)

The molecular genetics of haemochromatosis
nork: Shearman, J, et al.
Argitaratua: (1996)

The structure and function of HFE.
nork: Drakesmith, H, et al.
Argitaratua: (2000)

Pilot study of early diagnosis of hereditary haemochromatosis through systematic case finding in primary care.
nork: Emery, J, et al.
Argitaratua: (2002)

Pathogenesis Diagnostics and Treatment of Hereditary Haemochromatosis: A 150 Year-Long Understanding of an Iron Overload Disorder
nork: Anastasia Asimakopoulou, et al.
Argitaratua: (2017-11-01)

Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis
nork: Wei Zhang, et al.
Argitaratua: (2022-06-01)

Hereditary Hemochromatosis <it>(HFE) </it>genotypes in heart failure: Relation to etiology and prognosis
nork: Torp-Pedersen Christian, et al.
Argitaratua: (2010-07-01)

JUVENILE HAEMOCHROMATOSIS MUTATIONS ARE NOT THAT SIMPLE
nork: Bignell, P, et al.
Argitaratua: (2013)

Juvenile haemochromatosis in the Bangladeshi community
nork: Lok, C, et al.
Argitaratua: (2007)

Therapeutic monoclonal antibodies with a focus on hereditary angioedema
nork: Bruce L. Zuraw, et al.
Argitaratua: (2023-01-01)

Clinical applications of monoclonal antibodies.
nork: Mcmichael, A, et al.
Argitaratua: (1980)

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

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

Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation
nork: J Bryant, et al.
Argitaratua: (2009-04-01)

Screening for hereditary haemochromatosis in patients undergoing knee arthroplasty: a retrospective cohort study of 2,035 patients
nork: Elisha Krasin, et al.
Argitaratua: (2021-12-01)