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PUBMED FOR HANDHELDS

Journal Abstract Search


135 related items for PubMed ID: 10342073

  • 21. Heterozygosity for the C282Y mutation in the hemochromatosis gene is associated with increased serum iron, transferrin saturation, and hemoglobin in young women: a protective role against iron deficiency?
    Datz C, Haas T, Rinner H, Sandhofer F, Patsch W, Paulweber B.
    Clin Chem; 1998 Dec; 44(12):2429-32. PubMed ID: 9836708
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  • 23. Relationship of body iron stores to levels of serum ferritin, serum iron, unsaturated iron binding capacity and transferrin saturation in patients with iron storage disease.
    Beutler E, Felitti V, Ho NJ, Gelbart T.
    Acta Haematol; 2002 Dec; 107(3):145-9. PubMed ID: 11978935
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  • 24. Haptoglobin type neither influences iron accumulation in normal subjects nor predicts clinical presentation in HFE C282Y haemochromatosis: phenotype and genotype analysis.
    Carter K, Bowen DJ, McCune CA, Worwood M.
    Br J Haematol; 2003 Jul; 122(2):326-32. PubMed ID: 12846904
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  • 25. Severity of iron overload of proband determines serum ferritin levels in families with HFE-related hemochromatosis: the HEmochromatosis FAmily Study.
    Jacobs EM, Hendriks JC, van Deursen CT, Kreeftenberg HG, de Vries RA, Marx JJ, Stalenhoef AF, Verbeek AL, Swinkels DW.
    J Hepatol; 2009 Jan; 50(1):174-83. PubMed ID: 19008010
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  • 28. [Diagnosis of haemochromatosis].
    IJsselstijn L, van Houten AA, Weerkamp F.
    Ned Tijdschr Geneeskd; 2017 Jan; 161():D1438. PubMed ID: 29145899
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  • 29. Hereditary haemochromatosis in two cousins with cluster headache.
    Stovner LJ, Hagen K, Waage A, Bjerve KS.
    Cephalalgia; 2002 May; 22(4):317-9. PubMed ID: 12100096
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  • 34. Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes.
    Radio FC, Majore S, Aurizi C, Sorge F, Biolcati G, Bernabini S, Giotti I, Torricelli F, Giannarelli D, De Bernardo C, Grammatico P.
    Blood Cells Mol Dis; 2015 Jun; 55(1):71-5. PubMed ID: 25976471
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  • 36. Hereditary haemochromatosis.
    Janssen MC, Swinkels DW.
    Best Pract Res Clin Gastroenterol; 2009 Jun; 23(2):171-83. PubMed ID: 19414144
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  • 39. A diagnostic approach to hyperferritinemia with a non-elevated transferrin saturation.
    Adams PC, Barton JC.
    J Hepatol; 2011 Aug; 55(2):453-8. PubMed ID: 21354228
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  • 40. Epidemiology and diagnostic testing for hemochromatosis and iron overload.
    Adams PC.
    Int J Lab Hematol; 2015 May; 37 Suppl 1():25-30. PubMed ID: 25976957
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