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Items: 1 to 20 of 194

2.

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;122(3):646-51. Erratum in: Gastroenterology 2002 Apr;122(4):1191.

PMID:
11874997
3.

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.

4.

Effect of hemochromatosis genotype and lifestyle factors on iron and red cell indices in a community population.

Rossi E, Bulsara MK, Olynyk JK, Cullen DJ, Summerville L, Powell LW.

Clin Chem. 2001 Feb;47(2):202-8.

5.

Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.

Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.

Eur J Immunogenet. 2000 Jun;27(3):129-34.

PMID:
10940080
6.

Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.

Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD.

Isr Med Assoc J. 2004 Jan;6(1):30-3.

7.

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;114(2):474-84.

PMID:
11529872
8.

Testing for haemochromatosis in a liver clinic population: relationship between ethnic origin, HFE gene mutations, liver histology and serum iron markers.

Moodie SJ, Ang L, Stenner JM, Finlayson C, Khotari A, Levin GE, Maxwell JD.

Eur J Gastroenterol Hepatol. 2002 Mar;14(3):223-9.

PMID:
11953685
9.

Decreased iron burden in overweight C282Y homozygous women: Putative role of increased hepcidin production.

Desgrippes R, Lainé F, Morcet J, Perrin M, Manet G, Jezequel C, Bardou-Jacquet E, Ropert M, Deugnier Y.

Hepatology. 2013 May;57(5):1784-92. doi: 10.1002/hep.26261. Epub 2013 Apr 4.

PMID:
23322654
10.

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 2;341(10):718-24.

11.

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. doi: 10.1111/j.1751-553X.2007.00956.x.

PMID:
18665827
12.

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.

PMID:
9410475
13.

Genotypic/phenotypic correlations in genetic hemochromatosis: evolution of diagnostic criteria.

Adams PC, Chakrabarti S.

Gastroenterology. 1998 Feb;114(2):319-23.

PMID:
9453492
14.
15.
16.

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.

PMID:
17767550
17.

HFE based re-evaluation of heterozygous hemochromatosis.

Moirand R, Guyader D, Mendler MH, Jouanolle AM, Le Gall JY, David V, Brissot P, Deugnier Y.

Am J Med Genet. 2002 Sep 1;111(4):356-61.

PMID:
12210292
18.

Population screening for hemochromatosis: a study in 5370 Spanish blood donors.

Sánchez M, Villa M, Ingelmo M, Sanz C, Bruguera M, Ascaso C, Oliva R.

J Hepatol. 2003 Jun;38(6):745-50.

PMID:
12763366
19.
20.

Screening for iron overload in the Turkish population.

Barut G, Balci H, Bozdayi M, Hatemi I, Ozcelik D, Senturk H.

Dig Dis. 2003;21(3):279-85.

PMID:
14571105

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