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Items: 1 to 20 of 67

1.

The effect of transferrin polymorphisms on iron metabolism.

Lee PL, Ho NJ, Olson R, Beutler E.

Blood Cells Mol Dis. 1999 Oct-Dec;25(5-6):374-9.

PMID:
10660486
2.

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.

3.

Diagnosis of hemochromatosis in family members of probands: a comparison of phenotyping and HFE genotyping.

Barton JC, Rothenberg BE, Bertoli LF, Acton RT.

Genet Med. 1999 Mar-Apr;1(3):89-93.

PMID:
11336458
5.

The soluble transferrin receptor as a marker of iron homeostasis in normal subjects and in HFE-related hemochromatosis.

Brandão M, Oliveira JC, Bravo F, Reis J, Garrido I, Porto G.

Haematologica. 2005 Jan;90(1):31-7.

6.

Peripheral blood erythrocyte parameters in hemochromatosis: evidence for increased erythrocyte hemoglobin content.

Barton JC, Bertoli LF, Rothenberg BE.

J Lab Clin Med. 2000 Jan;135(1):96-104.

PMID:
10638700
7.
8.

HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors.

Arya N, Chakrabrati S, Hegele RA, Adams PC.

Blood Cells Mol Dis. 1999 Oct-Dec;25(5-6):354-7.

PMID:
10660483
9.

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.

10.
11.

Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.

Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.

Immunogenetics. 1998 Apr;47(5):404-10.

PMID:
9510559
12.

HFE downregulates iron uptake from transferrin and induces iron-regulatory protein activity in stably transfected cells.

Riedel HD, Muckenthaler MU, Gehrke SG, Mohr I, Brennan K, Herrmann T, Fitscher BA, Hentze MW, Stremmel W.

Blood. 1999 Dec 1;94(11):3915-21.

13.

A new polymorphism in the human HFE gene.

Höhler T, Leininger S, Schneider PM.

Immunogenetics. 1999 Aug;49(9):823-4. No abstract available.

PMID:
10398812
14.

Variation of iron loading expression in C282Y homozygous haemochromatosis probands and sib pairs.

Mura C, Le Gac G, Scotet V, Raguenes O, Mercier AY, Férec C.

J Med Genet. 2001 Sep;38(9):632-6. No abstract available.

15.
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17.

Impact of HLA-H mutations on iron stores in healthy elderly men and women.

Garry PJ, Montoya GD, Baumgartner RN, Liang HC, Williams TM, Brodie SG.

Blood Cells Mol Dis. 1997 Aug;23(2):277-87.

PMID:
9410471
18.

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.

PMID:
10207799
19.

Hepatic iron overload: direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis.

Press RD, Flora K, Gross C, Rabkin JM, Corless CL.

Am J Clin Pathol. 1998 May;109(5):577-84.

PMID:
9576576
20.

HFE, iron homeostasis and genetic hemochromatosis.

Cazzola M.

Haematologica. 2000 Apr;85(4):338-9. No abstract available.

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