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161 related items for PubMed ID: 22183642
1. Probability of C282Y homozygosity decreases as liver transaminase activities increase in participants with hyperferritinemia in the hemochromatosis and iron overload screening study. Adams PC, Speechley M, Barton JC, McLaren CE, McLaren GD, Eckfeldt JH. Hepatology; 2012 Jun; 55(6):1722-6. PubMed ID: 22183642 [Abstract] [Full Text] [Related]
2. Hemochromatosis and iron-overload screening in a racially diverse population. Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators. N Engl J Med; 2005 Apr 28; 352(17):1769-78. PubMed ID: 15858186 [Abstract] [Full Text] [Related]
3. HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening. Barton JC, Acton RT, Leiendecker-Foster C, Lovato L, Adams PC, McLaren GD, Eckfeldt JH, McLaren CE, Reboussin DM, Gordeuk VR, Speechley MR, Reiss JA, Press RD, Dawkins FW, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators. Genet Test; 2007 Apr 28; 11(3):269-75. PubMed ID: 17949288 [Abstract] [Full Text] [Related]
4. HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L. Adams PC, McLaren CE, Speechley M, McLaren GD, Barton JC, Eckfeldt JH. Can J Gastroenterol; 2013 Jul 28; 27(7):390-2. PubMed ID: 23862168 [Abstract] [Full Text] [Related]
5. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study. Adams PC, Pankow JS, Barton JC, Acton RT, Leiendecker-Foster C, McLaren GD, Speechley M, Eckfeldt JH. Circ Cardiovasc Genet; 2009 Feb 28; 2(1):34-7. PubMed ID: 20031565 [Abstract] [Full Text] [Related]
6. Determinants and characteristics of mean corpuscular volume and hemoglobin concentration in white HFE C282Y homozygotes in the hemochromatosis and iron overload screening study. McLaren CE, Barton JC, Gordeuk VR, Wu L, Adams PC, Reboussin DM, Speechley M, Chang H, Acton RT, Harris EL, Ruggiero AM, Castro O, Hemochromatosis and Iron Overload Screening Study Research Investigators. Am J Hematol; 2007 Oct 28; 82(10):898-905. PubMed ID: 17597476 [Abstract] [Full Text] [Related]
7. Serial serum ferritin measurements in untreated HFE C282Y homozygotes in the Hemochromatosis and Iron Overload Screening Study. Adams PC, Reboussin DM, Barton JC, Acton RT, Speechley M, Leiendecker-Foster C, Meenan R, Passmore L, McLaren CE, McLaren GD, Gordeuk V, Dawkins F, Eckfeldt JH. Int J Lab Hematol; 2008 Aug 28; 30(4):300-5. PubMed ID: 18665827 [Abstract] [Full Text] [Related]
8. Iron-overload-related disease in HFE hereditary hemochromatosis. Allen KJ, Gurrin LC, Constantine CC, Osborne NJ, Delatycki MB, Nicoll AJ, McLaren CE, Bahlo M, Nisselle AE, Vulpe CD, Anderson GJ, Southey MC, Giles GG, English DR, Hopper JL, Olynyk JK, Powell LW, Gertig DM. N Engl J Med; 2008 Jan 17; 358(3):221-30. PubMed ID: 18199861 [Abstract] [Full Text] [Related]
9. Predicting C282Y homozygote genotype for hemochromatosis using serum ferritin and transferrin saturation values from 44,809 participants of the HEIRS study. Lim A, Speechley M, Adams PC. Can J Gastroenterol Hepatol; 2014 Oct 17; 28(9):502-4. PubMed ID: 25314357 [Abstract] [Full Text] [Related]
10. Hemochromatosis mutations in the general population: iron overload progression rate. Andersen RV, Tybjaerg-Hansen A, Appleyard M, Birgens H, Nordestgaard BG. Blood; 2004 Apr 15; 103(8):2914-9. PubMed ID: 15070663 [Abstract] [Full Text] [Related]
11. Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study. McLaren CE, Barton JC, Eckfeldt JH, McLaren GD, Acton RT, Adams PC, Henkin LF, Gordeuk VR, Vulpe CD, Harris EL, Harrison BW, Reiss JA, Snively BM. Am J Hematol; 2010 Feb 15; 85(2):101-5. PubMed ID: 20095037 [Abstract] [Full Text] [Related]
12. Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) study. Acton RT, Barton JC, Passmore LV, Adams PC, Speechley MR, Dawkins FW, Sholinsky P, Reboussin DM, McLaren GD, Harris EL, Bent TC, Vogt TM, Castro O. Diabetes Care; 2006 Sep 15; 29(9):2084-9. PubMed ID: 16936157 [Abstract] [Full Text] [Related]
13. Tumor necrosis factor-alpha promoter variants and iron phenotypes in 785 hemochromatosis and iron overload screening (HEIRS) study participants. Acton RT, Barton JC, Leiendecker-Foster C, Zaun C, McLaren CE, Eckfeldt JH. Blood Cells Mol Dis; 2010 Apr 15; 44(4):252-6. PubMed ID: 20178892 [Abstract] [Full Text] [Related]
14. Liver diseases in the hemochromatosis and iron overload screening study. Adams PC, Passmore L, Chakrabarti S, Reboussin DM, Acton RT, Barton JC, McLaren GD, Eckfeldt JH, Dawkins FW, Gordeuk VR, Harris EL, Leiendecker-Foster C, Gossman E, Sholinsky P, Hemochromatosis and Iron Overload Screening Study Research Investigators. Clin Gastroenterol Hepatol; 2006 Jul 15; 4(7):918-23; quiz 807. PubMed ID: 16797244 [Abstract] [Full Text] [Related]
15. Thyroid-stimulating hormone and free thyroxine levels in persons with HFE C282Y homozygosity, a common hemochromatosis genotype: the HEIRS study. Barton JC, Leiendecker-Foster C, Reboussin DM, Adams PC, Acton RT, Eckfeldt JH, Hemochromatosis and Iron Overload Screening Study Research Investigators. Thyroid; 2008 Aug 15; 18(8):831-8. PubMed ID: 18651828 [Abstract] [Full Text] [Related]
16. Hereditary hemochromatosis: insights from the Hemochromatosis and Iron Overload Screening (HEIRS) Study. McLaren GD, Gordeuk VR. Hematology Am Soc Hematol Educ Program; 2009 Aug 15; ():195-206. PubMed ID: 20008199 [Abstract] [Full Text] [Related]
17. Correlates of hepcidin and NTBI according to HFE status in patients referred to a liver centre. Ryan E, Ryan JD, Russell J, Coughlan B, Tjalsma H, Swinkels DW, Stewart S, Crowe JP. Acta Haematol; 2015 Aug 15; 133(2):155-61. PubMed ID: 25277871 [Abstract] [Full Text] [Related]