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484 related items for PubMed ID: 16838333
21. Identification of new mutations of the HFE, hepcidin, and transferrin receptor 2 genes by denaturing HPLC analysis of individuals with biochemical indications of iron overload. Biasiotto G, Belloli S, Ruggeri G, Zanella I, Gerardi G, Corrado M, Gobbi E, Albertini A, Arosio P. Clin Chem; 2003 Dec; 49(12):1981-8. PubMed ID: 14633868 [Abstract] [Full Text] [Related]
22. Three kinships with ALAS2 P520L (c. 1559 C --> T) mutation, two in association with severe iron overload, and one with sideroblastic anemia and severe iron overload. Lee PL, Barton JC, Rao SV, Acton RT, Adler BK, Beutler E. Blood Cells Mol Dis; 2006 Dec; 36(2):292-7. PubMed ID: 16446107 [Abstract] [Full Text] [Related]
23. 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]
24. EASL clinical practice guidelines for HFE hemochromatosis. European Association For The Study Of The Livereasl@easloffice.eu. J Hepatol; 2010 Jul 28; 53(1):3-22. PubMed ID: 20471131 [Abstract] [Full Text] [Related]
28. Transferrin receptor-2 (TFR2) mutation Y250X in Alabama Caucasian and African American subjects with and without primary iron overload. Barton EH, West PA, Rivers CA, Barton JC, Acton RT. Blood Cells Mol Dis; 2001 Jul 28; 27(1):279-84. PubMed ID: 11358388 [Abstract] [Full Text] [Related]
33. The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic. Beutler E, Felitti V, Gelbart T, Ho N. Ann Intern Med; 2000 Sep 05; 133(5):329-37. PubMed ID: 10979877 [Abstract] [Full Text] [Related]
36. Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene. Altès A, Bach V, Ruiz A, Esteve A, Felez J, Remacha AF, Sardà MP, Baiget M. Ann Hematol; 2009 Oct 05; 88(10):951-5. PubMed ID: 19214511 [Abstract] [Full Text] [Related]