These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

105 related articles for article (PubMed ID: 32942924)

  • 1. Arthropathy in hereditary haemochromatosis segregates with elevated erythrocyte mean corpuscular volume.
    Rehman A; Carroll GJ; Powell LW; Ramm LE; Ramm GA; Olynyk JK
    Scand J Rheumatol; 2021 Mar; 50(2):139-142. PubMed ID: 32942924
    [No Abstract]   [Full Text] [Related]  

  • 2. Peripheral blood erythrocyte parameters in hemochromatosis: evidence for increased erythrocyte hemoglobin content.
    Barton JC; Bertoli LF; Rothenberg BE
    J Lab Clin Med; 2000 Jan; 135(1):96-104. PubMed ID: 10638700
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of HFE Haemochromatosis in the clinic and community using standard erythrocyte tests.
    Adris N; Hazeldine S; Bentley P; Trinder D; Chua ACG; Powell LW; Ramm LE; Ramm GA; Olynyk JK
    Blood Cells Mol Dis; 2019 Feb; 74():18-24. PubMed ID: 30340937
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Screening for hemochromatosis in routine medical care: an evaluation of mean corpuscular volume and mean corpuscular hemoglobin.
    Barton JC; Bertoli LF; Rothenberg BE
    Genet Test; 2000; 4(2):103-10. PubMed ID: 10953947
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The soluble transferrin receptor as a marker of iron homeostasis in normal subjects and in HFE-related hemochromatosis.
    Brandão M; Oliveira JC; Bravo F; Reis J; Garrido I; Porto G
    Haematologica; 2005 Jan; 90(1):31-7. PubMed ID: 15642666
    [TBL] [Abstract][Full Text] [Related]  

  • 6. VCAM-1 serum levels are associated with arthropathy in hereditary haemochromatosis.
    Nell-Duxneuner V; Axmann R; Husar-Memmer E; Dallos T; Datz C; Stadlmayr A; Aigner E; Englbrecht M; Schett G; Zwerina J
    Ann Rheum Dis; 2013 Dec; 72(12):2006-10. PubMed ID: 23599437
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Primary osteoarthritis in the ankle joint is associated with finger metacarpophalangeal osteoarthritis and the H63D mutation in the HFE gene: evidence for a hemochromatosis-like polyarticular osteoarthritis phenotype.
    Carroll GJ
    J Clin Rheumatol; 2006 Jun; 12(3):109-13. PubMed ID: 16755236
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Searching for hereditary hemochromatosis.
    Laudicina RJ
    Clin Lab Sci; 2006; 19(3):174-83. PubMed ID: 16910235
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry.
    Beutler E; Felitti V; Gelbart T; Waalen J
    Br J Haematol; 2003 Mar; 120(5):887-93. PubMed ID: 12614226
    [TBL] [Abstract][Full Text] [Related]  

  • 10. HFE mutations in patients with hereditary haemochromatosis in Sweden.
    Cardoso EM; Stål P; Hagen K; Cabeda JM; Esin S; de Sousa M; Hultcrantz R
    J Intern Med; 1998 Mar; 243(3):203-8. PubMed ID: 9627157
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Effect of C282Y genotype on self-reported musculoskeletal complications in hereditary hemochromatosis.
    Camacho A; Funck-Brentano T; Simão M; Cancela L; Ottaviani S; Cohen-Solal M; Richette P
    PLoS One; 2015; 10(3):e0122817. PubMed ID: 25822977
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Underdiagnosis of hereditary haemochromatosis: lack of presentation or penetration?
    Ryan E; Byrnes V; Coughlan B; Flanagan AM; Barrett S; O'Keane JC; Crowe J
    Gut; 2002 Jul; 51(1):108-12. PubMed ID: 12077102
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Combined effect of hemoglobin and mean corpuscular volume levels on incident metabolic syndrome: A population-based cohort study.
    Tanaka M; Okada H; Hashimoto Y; Kumagai M; Nishimura H; Fukui M
    Clin Nutr ESPEN; 2020 Dec; 40():314-319. PubMed ID: 33183556
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synovial immunopathology in haemochromatosis arthropathy.
    Heiland GR; Aigner E; Dallos T; Sahinbegovic E; Krenn V; Thaler C; Weiss G; Distler JH; Datz C; Schett G; Zwerina J
    Ann Rheum Dis; 2010 Jun; 69(6):1214-9. PubMed ID: 19933745
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Highly sensitivity adhesion molecules detection in hereditary haemochromatosis patients reveals altered expression.
    Norris S; White M; Mankan AK; Lawless MW
    Int J Immunogenet; 2010 Apr; 37(2):125-33. PubMed ID: 20193033
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary hemochromatosis is characterized by a clinically definable arthropathy that correlates with iron load.
    Carroll GJ; Breidahl WH; Bulsara MK; Olynyk JK
    Arthritis Rheum; 2011 Jan; 63(1):286-94. PubMed ID: 20954257
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Compound heterozygous hemochromatosis genotype predicts increased iron and erythrocyte indices in women.
    Rossi E; Olynyk JK; Cullen DJ; Papadopoulos G; Bulsara M; Summerville L; Powell LW
    Clin Chem; 2000 Feb; 46(2):162-6. PubMed ID: 10657371
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
    Lawless MW; White M; Mankan AK; O'Dwyer MJ; Norris S
    Tissue Antigens; 2007 Oct; 70(4):294-300. PubMed ID: 17767550
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Confirmation of two major polyarticular osteoarthritis (POA) phenotypes--differentiation on the basis of joint topography.
    Carroll GJ; Breidahl WH; Jazayeri J
    Osteoarthritis Cartilage; 2009 Jul; 17(7):891-5. PubMed ID: 19264516
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.
    Bittencourt PL; Palácios SA; Couto CA; Cançado EL; Carrilho FJ; Laudanna AA; Kalil J; Gayotto LC; Goldberg AC
    Braz J Med Biol Res; 2002 Mar; 35(3):329-35. PubMed ID: 11887210
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.