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Journal Abstract Search
98 related items for PubMed ID: 11087882
1. Disease-related conditions in relatives of patients with hemochromatosis. Bulaj ZJ, Ajioka RS, Phillips JD, LaSalle BA, Jorde LB, Griffen LM, Edwards CQ, Kushner JP. N Engl J Med; 2000 Nov 23; 343(21):1529-35. PubMed ID: 11087882 [Abstract] [Full Text] [Related]
2. Screening for hemochromatosis in asymptomatic subjects with or without a family history. Powell LW, Dixon JL, Ramm GA, Purdie DM, Lincoln DJ, Anderson GJ, Subramaniam VN, Hewett DG, Searle JW, Fletcher LM, Crawford DH, Rodgers H, Allen KJ, Cavanaugh JA, Bassett ML. Arch Intern Med; 2006 Feb 13; 166(3):294-301. PubMed ID: 16476869 [Abstract] [Full Text] [Related]
3. High prevalence of a screening-detected, HFE-unrelated, mild idiopathic iron overload in Northern Italy. Barosi G, Salvaneschi L, Grasso M, Martinetti M, Marchetti M, Bodini U, Reggiani A, D'Agostino F, Nalli G, Degiuli A, De Silvestri A, Arbustini E. Haematologica; 2002 May 13; 87(5):472-8. PubMed ID: 12010659 [Abstract] [Full Text] [Related]
4. Prevalence of hemochromatosis among 11,065 presumably healthy blood donors. Edwards CQ, Griffen LM, Goldgar D, Drummond C, Skolnick MH, Kushner JP. N Engl J Med; 1988 May 26; 318(21):1355-62. PubMed ID: 3367936 [Abstract] [Full Text] [Related]
6. Alcoholism in hereditary hemochromatosis revisited: prevalence and clinical consequences among homozygous siblings. Adams PC, Agnew S. Hepatology; 1996 Apr 26; 23(4):724-7. PubMed ID: 8666324 [Abstract] [Full Text] [Related]
7. Clinical and biochemical abnormalities in people heterozygous for hemochromatosis. Bulaj ZJ, Griffen LM, Jorde LB, Edwards CQ, Kushner JP. N Engl J Med; 1996 Dec 12; 335(24):1799-805. PubMed ID: 8943161 [Abstract] [Full Text] [Related]
8. The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: an update of clinical and immunological data from 70 C282Y homozygous subjects. Cruz E, Melo G, Lacerda R, Almeida S, Porto G. Blood Cells Mol Dis; 2006 Dec 12; 37(1):33-9. PubMed ID: 16762569 [Abstract] [Full Text] [Related]
10. Assessment of silent liver fibrosis in hemochromatosis C282Y homozygotes with normal transaminase levels. Beaton M, Adams PC. Clin Gastroenterol Hepatol; 2008 Jun 12; 6(6):713-4. PubMed ID: 18550006 [Abstract] [Full Text] [Related]
11. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload? de Diego C, Opazo S, Murga MJ, Martínez-Castro P. Eur J Haematol; 2007 Jan 12; 78(1):66-71. PubMed ID: 17042772 [Abstract] [Full Text] [Related]
14. Diagnosis of hemochromatosis in young subjects: predictive accuracy of biochemical screening tests. Bassett ML, Halliday JW, Ferris RA, Powell LW. Gastroenterology; 1984 Sep 12; 87(3):628-33. PubMed ID: 6745616 [Abstract] [Full Text] [Related]
15. Comparison of stainable liver iron between symptomatic and asymptomatic hemochromatosis homozygotes and their homozygous relatives. Edwards CQ, Griffen LM, Kushner JP. Am J Med Sci; 1991 Jan 12; 301(1):44-6. PubMed ID: 1994729 [Abstract] [Full Text] [Related]
16. Abdominal pain and cirrhosis at diagnosis of hemochromatosis: Analysis of 219 referred probands with HFE p.C282Y homozygosity and a literature review. Barton JC, Barton JC, Patel N, McLaren GD. PLoS One; 2021 Jan 12; 16(12):e0261690. PubMed ID: 34932603 [Abstract] [Full Text] [Related]
17. Iron-overload-related disease in HFE hereditary hemochromatosis. Waalen J, Beutler E. N Engl J Med; 2008 May 22; 358(21):2293-4; author reply 2294-5. PubMed ID: 18499578 [No Abstract] [Full Text] [Related]
18. [Diagnosis of iron overload]. Deugnier Y, Gandon Y, Juhel C, Olivié D, Jouanolle AM, Turlin B. Rev Prat; 2006 Dec 15; 56(19):2118-22. PubMed ID: 17416048 [Abstract] [Full Text] [Related]
19. Liver fibrosis in genetic hemochromatosis. Respective roles of iron and non-iron-related factors in 127 homozygous patients. Loréal O, Deugnier Y, Moirand R, Lauvin L, Guyader D, Jouanolle H, Turlin B, Lescoat G, Brissot P. J Hepatol; 1992 Sep 15; 16(1-2):122-7. PubMed ID: 1484146 [Abstract] [Full Text] [Related]