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Items: 1 to 20 of 409

1.

Diagnosis of hemochromatosis.

Powell LW, George DK, McDonnell SM, Kowdley KV.

Ann Intern Med. 1998 Dec 1;129(11):925-31. Review.

PMID:
9867744
2.

Review article: the screening, diagnosis and optimal management of haemochromatosis.

George DK, Powell LW.

Aliment Pharmacol Ther. 1997 Aug;11(4):631-9. Review.

3.

Management of hemochromatosis. Hemochromatosis Management Working Group.

Barton JC, McDonnell SM, Adams PC, Brissot P, Powell LW, Edwards CQ, Cook JD, Kowdley KV.

Ann Intern Med. 1998 Dec 1;129(11):932-9. Review.

PMID:
9867745
4.

[Diagnosis and treatment of primary hemochromatosis].

Swinkels DW, Marx JJ.

Ned Tijdschr Geneeskd. 1999 Jul 3;143(27):1404-8. Review. Dutch.

PMID:
10422553
5.

[Hemochromatosis--from an underdiagnosed curiosity to a common disease].

Hagve TA, Asberg A, Ulvik R, Borch-Iohnsen B, Thorstensen K.

Tidsskr Nor Laegeforen. 2009 Apr 30;129(9):863-6. doi: 10.4045/tidsskr.08.0084. Review. Norwegian.

7.

[Hereditary hemocromatosis].

Franchini M, Veneri D.

Recenti Prog Med. 2004 Oct;95(10):457-62. Italian.

PMID:
15560291
8.

Usefulness and limitations of laboratory and hepatic imaging studies in iron-storage disease.

Bonkovsky HL, Slaker DP, Bills EB, Wolf DC.

Gastroenterology. 1990 Oct;99(4):1079-91.

PMID:
2394329
9.

HFE genotype in patients with hemochromatosis and other liver diseases.

Bacon BR, Olynyk JK, Brunt EM, Britton RS, Wolff RK.

Ann Intern Med. 1999 Jun 15;130(12):953-62.

PMID:
10383365
10.

Diagnosis of hemochromatosis in young subjects: predictive accuracy of biochemical screening tests.

Bassett ML, Halliday JW, Ferris RA, Powell LW.

Gastroenterology. 1984 Sep;87(3):628-33.

PMID:
6745616
11.

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.

PMID:
16476869
12.

Management of hereditary hemochromatosis.

Phatak PD, Cappuccio JD.

Blood Rev. 1994 Dec;8(4):193-8. Review.

PMID:
7888827
13.

[Significance of "minor" genetic mutations in hereditary hemochromatosis: 2 case reports].

Maccari S, Plancher AC.

Ann Ital Med Int. 2000 Jul-Sep;15(3):221-5. Italian.

PMID:
11059064
14.

Normal serum ferritin concentrations in precirrhotic hemochromatosis.

Wands JR, Rowe JA, Mezey SE, Waterbury LA, Wright JR, Halliday JW, Isselbacher KJ, Powell LW.

N Engl J Med. 1976 Feb 5;294(6):302-5.

PMID:
1246269
15.

[Primary hemochromatosis in asymptomatic young patients].

Muñoz Sánchez MM, Núñez Martínez O, Torres Orgaz A, del Castillo Rueda A, de Portugal Alvarez J.

An Med Interna. 2000 Jan;17(1):9-12. Spanish.

PMID:
10730398
16.

Hemochromatosis. Common genes, uncommon illness?

Harrison H, Adams PC.

Can Fam Physician. 2002 Aug;48:1326-33. Review.

17.
18.

Hereditary haemochromatosis: detection and management.

Vautier G, Murray M, Olynyk JK.

Med J Aust. 2001 Oct 15;175(8):418-21. Review.

PMID:
11700835
19.

[Diagnosis and treatment of genetic hemochromatosis].

Moirand R, Guillygomarc'h A, Brissot P, Deugnier Y.

Rev Prat. 2000 May 1;50(9):977-82. Review. French.

PMID:
10865497
20.

Diagnosis and management of genetic haemochromatosis.

Dooley JS.

Best Pract Res Clin Haematol. 2002 Jun;15(2):277-93. Review.

PMID:
12401308
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