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513 related items for PubMed ID: 16979952
1. The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis. Walsh A, Dixon JL, Ramm GA, Hewett DG, Lincoln DJ, Anderson GJ, Subramaniam VN, Dodemaide J, Cavanaugh JA, Bassett ML, Powell LW. Clin Gastroenterol Hepatol; 2006 Nov; 4(11):1403-10. PubMed ID: 16979952 [Abstract] [Full Text] [Related]
2. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases. Sham RL, Ou CY, Cappuccio J, Braggins C, Dunnigan K, Phatak PD. Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475 [Abstract] [Full Text] [Related]
3. [Molecular genetic diagnostics and screening of hereditary hemochromatosis]. Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S. Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764 [Abstract] [Full Text] [Related]
4. Differences in hepatic phenotype between hemochromatosis patients with HFE C282Y homozygosity and other HFE genotypes. Cheng R, Barton JC, Morrison ED, Phatak PD, Krawitt EL, Gordon SC, Kowdley KV. J Clin Gastroenterol; 2009 Jul; 43(6):569-73. PubMed ID: 19359997 [Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
6. HFE mutations, hepatic iron, and fibrosis: ethnic-specific association of NASH with C282Y but not with fibrotic severity. Chitturi S, Weltman M, Farrell GC, McDonald D, Kench J, Liddle C, Samarasinghe D, Lin R, Abeygunasekera S, George J. Hepatology; 2002 Jul; 36(1):142-9. PubMed ID: 12085358 [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; 30(4):300-5. PubMed ID: 18665827 [Abstract] [Full Text] [Related]
8. A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria. Brissot P, Moirand R, Jouanolle AM, Guyader D, Le Gall JY, Deugnier Y, David V. J Hepatol; 1999 Apr; 30(4):588-93. PubMed ID: 10207799 [Abstract] [Full Text] [Related]
9. Significance of H63D homozygosity in a Basque population with hemochromatosis. Castiella A, Zapata E, de Juan MD, Otazua P, Fernandez J, Zubiaurre L, Arriola JA, Gipuzkoa Hemochromatosis Group. J Gastroenterol Hepatol; 2010 Jul; 25(7):1295-8. PubMed ID: 20594259 [Abstract] [Full Text] [Related]
10. Screening for iron overload in the Turkish population. Barut G, Balci H, Bozdayi M, Hatemi I, Ozcelik D, Senturk H. Dig Dis; 2003 Jul; 21(3):279-85. PubMed ID: 14571105 [Abstract] [Full Text] [Related]
11. Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturation. Velati C, Marlianici E, Rigamonti D, Barillari G, Chiavilli F, Fugiani P, Garozzo G, Lancieri M, Rinaldi S, Testa D, Sampietro M, Tavazzi D, Delbini P, Fargion S, Fiorelli G. Hematol J; 2003 Jul; 4(6):436-40. PubMed ID: 14671617 [Abstract] [Full Text] [Related]
12. 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; 2(1):34-7. PubMed ID: 20031565 [Abstract] [Full Text] [Related]
13. 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]
14. A population-based study of the clinical expression of the hemochromatosis gene. Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell LW. N Engl J Med; 1999 Sep 02; 341(10):718-24. PubMed ID: 10471457 [Abstract] [Full Text] [Related]
15. Clinical characteristics of HFE C282Y/H63D compound heterozygotes identified in a specialty practice: key differences from HFE C282Y homozygotes. Singal M, Mahmoud A, Phatak PD. Expert Rev Hematol; 2024 Sep 02; 17(4-5):145-152. PubMed ID: 38551816 [Abstract] [Full Text] [Related]
16. Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy. Cassanelli S, Pignatti E, Montosi G, Garuti C, Mariano M, Campioli D, Carbonieri A, Baldini E, Pietrangelo A. J Hepatol; 2001 Apr 02; 34(4):523-8. PubMed ID: 11394651 [Abstract] [Full Text] [Related]
17. HFE genotype in patients with hemochromatosis and other liver diseases. Bacon BR, Olynyk JK, Brunt EM, Britton RS, Wolff RK. Ann Intern Med; 1999 Jun 15; 130(12):953-62. PubMed ID: 10383365 [Abstract] [Full Text] [Related]
18. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation. Gochee PA, Powell LW, Cullen DJ, Du Sart D, Rossi E, Olynyk JK. Gastroenterology; 2002 Mar 15; 122(3):646-51. PubMed ID: 11874997 [Abstract] [Full Text] [Related]
19. HFE mutations, iron deficiency and overload in 10,500 blood donors. Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M. Br J Haematol; 2001 Aug 15; 114(2):474-84. PubMed ID: 11529872 [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 15; 35(3):329-35. PubMed ID: 11887210 [Abstract] [Full Text] [Related] Page: [Next] [New Search]