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

Zobrazit další vydání (1)

Podrobná bibliografie
Hlavní autoři:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
Médium:	Journal article
Vydáno:	1998

Podobné jednotky

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.
Autor: Bastin, J, a další
Vydáno: (1998)

HFE-Associated Hereditary Haemochromatosis
Autor: Emmeke J Eijkelkamp, a další
Vydáno: (2000-01-01)

Identification of new ligands for the haemochromatosis protein HFE
Autor: Drakesmith, H, a další
Vydáno: (2007)

Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload.
Autor: Townsend, A, a další
Vydáno: (2002)

Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload
Autor: Townsend, A, a další
Vydáno: (2002)

Clinical haemochromatosis in HFE mutation carriers.
Autor: Cox, T, a další
Vydáno: (2002)

Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis
Autor: Barton David E, a další
Vydáno: (2006-11-01)

Factors influencing disease phenotype and penetrance in HFE haemochromatosis.
Autor: Rochette, J, a další
Vydáno: (2010)

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
Autor: Merryweather-Clarke, A, a další
Vydáno: (2003)

Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience
Autor: Robson, K, a další
Vydáno: (2000)

Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis.
Autor: Sebastiani, G, a další
Vydáno: (2003)

RECRUITMENT OF PATIENTS WITH HEREDITARY HAEMOCHROMATOSIS AS BLOOD DONORS
Autor: Marko Cukjati, a další
Vydáno: (2004-12-01)

Hereditary haemochromatosis, haemophagocytic lymphohistiocytosis and COVID-19
Autor: Matthew J. Riley, a další
Vydáno: (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
Autor: M. Vázquez Romero, a další
Vydáno: (2005-08-01)

The hemochromatosis protein HFE inhibits iron export from macrophages.
Autor: Drakesmith, H, a další
Vydáno: (2002)

Public health aspects of genetic screening for hereditary haemochromatosis in Australia
Autor: Dorota M. Gertig, a další
Vydáno: (2002-12-01)

The development of polycythemia vera after phlebotomy treatment for hereditary haemochromatosis
Autor: Erik JM vanBommel, a další
Vydáno: (2021-08-01)

Genetic mutations, diagnostic methods, and therapies related to hereditary haemochromatosis
Autor: Karina Marini Aguiar, a další
Vydáno: (2014-03-01)

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

In vitro binding of HFE to the cation-independent mannose-6 phosphate receptor.
Autor: Schimanski, L, a další
Vydáno: (2009)

Ultrasound verified inflammation and structural damage in patients with hereditary haemochromatosis-related arthropathy
Autor: Christian Dejaco, a další
Vydáno: (2017-10-01)

Primary Biliary Cirrhosis-Specific Antimitochondrial Antibodies in Neonatal Haemochromatosis
Autor: Daniel S. Smyk, a další
Vydáno: (2013-01-01)

Inflammation can increase hepcidin in HFE‐hereditary hemochromatosis
Autor: Wenke Moris, a další
Vydáno: (2021-05-01)

Hereditary haemochromatosis: pilot study of case-finding approach to early diagnosis in primary care.
Autor: Emery, J, a další
Vydáno: (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.
Autor: Robson, K, a další
Vydáno: (2004)

Infertility: Consider haemochromatosis?
Autor: Lok, C, a další
Vydáno: (2007)

The molecular genetics of haemochromatosis
Autor: Shearman, J, a další
Vydáno: (1996)

The structure and function of HFE.
Autor: Drakesmith, H, a další
Vydáno: (2000)

Pilot study of early diagnosis of hereditary haemochromatosis through systematic case finding in primary care.
Autor: Emery, J, a další
Vydáno: (2002)

Pathogenesis Diagnostics and Treatment of Hereditary Haemochromatosis: A 150 Year-Long Understanding of an Iron Overload Disorder
Autor: Anastasia Asimakopoulou, a další
Vydáno: (2017-11-01)

Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis
Autor: Wei Zhang, a další
Vydáno: (2022-06-01)

Hereditary Hemochromatosis <it>(HFE) </it>genotypes in heart failure: Relation to etiology and prognosis
Autor: Torp-Pedersen Christian, a další
Vydáno: (2010-07-01)

JUVENILE HAEMOCHROMATOSIS MUTATIONS ARE NOT THAT SIMPLE
Autor: Bignell, P, a další
Vydáno: (2013)

Juvenile haemochromatosis in the Bangladeshi community
Autor: Lok, C, a další
Vydáno: (2007)

Therapeutic monoclonal antibodies with a focus on hereditary angioedema
Autor: Bruce L. Zuraw, a další
Vydáno: (2023-01-01)

Clinical applications of monoclonal antibodies.
Autor: Mcmichael, A, a další
Vydáno: (1980)

Erratum: Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease and secondary iron overload (Lancet (March 2) (786))
Autor: Townsend, A, a další
Vydáno: (2002)

Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease, and secondary iron overload (vol 359, pg 786, 2002)
Autor: Townsend, A, a další
Vydáno: (2002)

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

Screening for hereditary haemochromatosis in patients undergoing knee arthroplasty: a retrospective cohort study of 2,035 patients
Autor: Elisha Krasin, a další
Vydáno: (2021-12-01)