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Similar articles for PubMed (Select 10681280)

1.

Screening for hereditary hemochromatosis in siblings and children of affected patients. A cost-effectiveness analysis.

El-Serag HB, Inadomi JM, Kowdley KV.

Ann Intern Med. 2000 Feb 15;132(4):261-9.

PMID:
10681280
2.

Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.

Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT.

Blood Cells Mol Dis. 1999 Jun-Aug;25(3-4):147-55.

PMID:
10575540
3.

[Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].

Himmelmann A, Bortoluzzi L, Jansen S, Fehr J.

Schweiz Med Wochenschr. 2000 Aug 8;130(31-32):1112-9. German.

PMID:
11008304
4.

[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. Slovak.

PMID:
16871764
5.

[Screening for hereditary HFE hemochromatosis].

Deugnier Y, Jouanolle AM.

Presse Med. 2007 Sep;36(9 Pt 2):1292-4. Epub 2007 Jun 4. French.

PMID:
17544612
6.

Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.

Hellerbrand C, Bosserhoff AK, Seegers S, Lingner G, Wrede C, Lock G, Schölmerich J, Büttner R.

Scand J Gastroenterol. 2001 Nov;36(11):1211-6.

PMID:
11686223
7.

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;35(3):329-35.

8.

Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.

Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D, Schved JF.

Blood Cells Mol Dis. 2001 Jan-Feb;27(1):290-3.

PMID:
11358390
9.

Nonexpressing homozygotes for C282Y hemochromatosis: minority or majority of cases?

Adams PC.

Mol Genet Metab. 2000 Sep-Oct;71(1-2):81-6. Review.

PMID:
11001800
10.

Genetic testing for HFE hemochromatosis in Australia: the value of testing relatives of simple heterozygotes.

Cavanaugh JA, Wilson SR, Bassett ML.

J Gastroenterol Hepatol. 2002 Jul;17(7):800-3.

PMID:
12121511
11.

A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese origin.

Steiner M, Ocran K, Genschel J, Meier P, Gerl H, Ventz M, Schneider ML, Büttner C, Wadowska K, Kerner W, Schuff-Werner P, Lochs H, Schmidt H.

Gastroenterology. 2002 Mar;122(3):789-95.

PMID:
11875012
12.
13.

A primer for predicting risk of disease in HFE-linked hemochromatosis.

Adams PC, Walker AP, Acton RT.

Genet Test. 2001 Winter;5(4):311-6.

PMID:
11960576
14.

Hemochromatosis in Ireland and HFE.

Ryan E, O'keane C, Crowe J.

Blood Cells Mol Dis. 1998 Dec;24(4):428-32.

PMID:
9851896
15.

Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?

Cadet E, Capron D, Gallet M, Omanga-Léké ML, Boutignon H, Julier C, Robson KJ, Rochette J.

J Med Genet. 2005 May;42(5):390-5.

16.

A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.

Jouanolle AM, Fergelot P, Gandon G, Yaouanq J, Le Gall JY, David V.

Hum Genet. 1997 Oct;100(5-6):544-7.

PMID:
9341868
17.

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
18.

Cost-effectiveness of microsatellite instability screening as a method for detecting hereditary nonpolyposis colorectal cancer.

Ramsey SD, Clarke L, Etzioni R, Higashi M, Berry K, Urban N.

Ann Intern Med. 2001 Oct 16;135(8 Pt 1):577-88.

PMID:
11601929
19.
20.

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.

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