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Results: 1 to 20 of 103

Similar articles for PubMed (Select 1895049)

1.

Screening for haemochromatosis: prevalence among Danish blood donors.

Wiggers P, Dalhøj J, Kiaer H, Ring-Larsen H, Petersen PH, Blaabjerg O, Hørder M.

J Intern Med. 1991 Sep;230(3):265-70.

PMID:
1895049
2.

Lessons from a survey of genotyping for hereditary haemochromatosis.

Francis S, Thachil J.

J Clin Pathol. 2015 Jul;68(7):578. doi: 10.1136/jclinpath-2015-202977. Epub 2015 May 2. No abstract available.

PMID:
25935547
3.

Pattern of care of blood donors with early-uncomplicated hereditary haemochromatosis in a Swiss blood donation centre.

Stefashyna O, Stern M, Infanti L, Holbro A, Tichelli A, Buser A, O'Meara A.

Vox Sang. 2014 Feb;106(2):111-7. doi: 10.1111/vox.12078. Epub 2013 Sep 2.

PMID:
23992555
4.

[Erythrocytapheresis for hereditary haemochromatosis].

Rombout-Sestrienkova E, van Deursen CT, Janssen MC, van Kraaij MG, de Leeuw PW, Koek GH.

Ned Tijdschr Geneeskd. 2012;156(26):A4745. Dutch.

PMID:
22759710
5.

Hereditary haemochromatosis: a tale of eight siblings.

Pande SD, Ariyaratnam R, Burke MJ.

Clin Med. 2009 Dec;9(6):624-6.

PMID:
20095315
6.

Ferritin and increased vs upper reference interval tibc saturation to identify increased iron stores in African Americans.

Onyekwere OC, Kamineni P, Johnson-Largent TN, Fadojutimi-Akinsiku M, Dawkins FW, Gordeuk VR.

Clin Chim Acta. 2009 Jul;405(1-2):71-5. doi: 10.1016/j.cca.2009.04.001. Epub 2009 Apr 9.

PMID:
19362082
7.

Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.

Pedersen P, Milman N.

Ann Hematol. 2009 Aug;88(8):775-84. doi: 10.1007/s00277-008-0679-1. Epub 2009 Jan 22.

PMID:
19159930
8.

Detection of treatable neonatal liver disease by expanded newborn screening.

Mackay RJ, Bratkovic D, Couper R, Davidson GP, Fahy R, Fletcher JM, Ranieri E.

J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S271-3. doi: 10.1007/s10545-008-0842-9. Epub 2008 Oct 15.

PMID:
18855117
9.

The natural history of serum iron indices for HFE C282Y homozygosity associated with hereditary hemochromatosis.

Gurrin LC, Osborne NJ, Constantine CC, McLaren CE, English DR, Gertig DM, Delatycki MB, Southey MC, Hopper JL, Giles GG, Anderson GJ, Olynyk JK, Powell LW, Allen KJ; HealthIron Study Investigators.

Gastroenterology. 2008 Dec;135(6):1945-52. doi: 10.1053/j.gastro.2008.08.056. Epub 2008 Sep 13.

PMID:
18848943
10.

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
11.

Serum ferritin and transferrin saturation in Asians and Pacific Islanders.

Harris EL, McLaren CE, Reboussin DM, Gordeuk VR, Barton JC, Acton RT, McLaren GD, Vogt TM, Snively BM, Leiendecker-Foster C, Holup JL, Passmore LV, Eckfeldt JH, Lin E, Adams PC.

Arch Intern Med. 2007 Apr 9;167(7):722-6.

PMID:
17420432
12.

Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) study.

Acton RT, Barton JC, Passmore LV, Adams PC, Speechley MR, Dawkins FW, Sholinsky P, Reboussin DM, McLaren GD, Harris EL, Bent TC, Vogt TM, Castro O.

Diabetes Care. 2006 Sep;29(9):2084-9.

PMID:
16936157
13.

Searching for hereditary hemochromatosis.

Laudicina RJ.

Clin Lab Sci. 2006 Summer;19(3):174-83.

PMID:
16910235
14.

[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
15.

Liver diseases in the hemochromatosis and iron overload screening study.

Adams PC, Passmore L, Chakrabarti S, Reboussin DM, Acton RT, Barton JC, McLaren GD, Eckfeldt JH, Dawkins FW, Gordeuk VR, Harris EL, Leiendecker-Foster C, Gossman E, Sholinsky P; Hemochromatosis and Iron Overload Screening Study Research Investigators.

Clin Gastroenterol Hepatol. 2006 Jul;4(7):918-23; quiz 807.

PMID:
16797244
16.

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
17.

Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in whites and blacks in the Hemochromatosis and Iron Overload Screening Study.

Barton JC, Acton RT, Dawkins FW, Adams PC, Lovato L, Leiendecker-Foster C, McLaren CE, Reboussin DM, Speechley MR, Gordeuk VR, McLaren GD, Sholinsky P, Harris EL.

Genet Test. 2005 Fall;9(3):231-41.

PMID:
16225403
19.

Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).

Martinelli AL, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho L, Zucoloto S, Rodrigues S, Zago M.

Genet Mol Res. 2005 Mar 31;4(1):31-8.

20.

Hereditary hemochromatosis: population screening based on phenotype in Brazilian blood donors.

Barbosa KV, de Souza AF, Chebli JM, Proietti FA, Meirelles RS, de Souza JL.

J Clin Gastroenterol. 2005 May-Jun;39(5):430-4.

PMID:
15815212
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