PubMed

Correction: summary for patients on genes for hemochromatosis.

Herbert V.

Ann Intern Med. 2001 Apr 17;134(8):715. No abstract available. PMID: 11304115 [PubMed - indexed for MEDLINE]Related articles

Genetic screening for common mutations: lessons from hereditary hemochromatosis.

Njajou OT, Alizadeh BZ, van Duijn CM.

Eur J Epidemiol. 2003;18(1):3-4. No abstract available. PMID: 12705616 [PubMed - indexed for MEDLINE]Related articles

HFE genotype frequencies in consecutive reference laboratory specimens: comparisons among referral sources and association with initial diagnosis.

Acton RT, Barton JC.

Genet Test. 2001 Winter;5(4):299-306.PMID: 11960574 [PubMed - indexed for MEDLINE]Related articles

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 [PubMed - indexed for MEDLINE]Related articles

Iron overload and prolonged ingestion of iron supplements: clinical features and mutation analysis of hemochromatosis-associated genes in four cases.

Barton JC, Lee PL, West C, Bottomley SS.

Am J Hematol. 2006 Oct;81(10):760-7.PMID: 16838333 [PubMed - indexed for MEDLINE]Related articles

Absence of hemochromatosis associated Cys282Tyr HFE gene mutation and low frequency of hemochromatosis phenotype in nonalcoholic chronic liver disease patients in India.

Thakur V, Guptan RC, Hashmi AZ, Sakhuja P, Malhotra V, Sarin SK.

J Gastroenterol Hepatol. 2004 Jan;19(1):86-90.PMID: 14675248 [PubMed - indexed for MEDLINE]Related articles

Hemochromatosis mutations C282Y and H63D in 'cis' phase.

Best LG, Harris PE, Spriggs EL.

Clin Genet. 2001 Jul;60(1):68-72.PMID: 11531973 [PubMed - indexed for MEDLINE]Related articles

Hemochromatosis mutations are not linked to dilated cardiomyopathy in Israeli patients.

Goland S, Beilinson N, Kaftouri A, Shimoni S, Caspi A, Malnick SD.

Eur J Heart Fail. 2004 Aug;6(5):547-50.PMID: 15302000 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 14740507 [PubMed - indexed for MEDLINE]Related articlesFree article

Hemochromatosis (HFE) gene mutations in Brazilian chronic hemodialysis patients.

Perícole FV, Alves MA, Saad ST, Costa FF.

Braz J Med Biol Res. 2005 Sep;38(9):1321-4. Epub 2005 Aug 26.PMID: 16138214 [PubMed - indexed for MEDLINE]Related articlesFree article

C282Y and H63D mutation of the hemochromatosis gene in German porphyria cutanea tarda patients.

Tannapfel A, Stölzel U, Köstler E, Melz S, Richter M, Keim V, Schuppan D, Wittekind C.

Virchows Arch. 2001 Jul;439(1):1-5.PMID: 11499833 [PubMed - indexed for MEDLINE]Related articles

A rare case of a patient heterozygous for the hemochromatosis mutation C282Y and homozygous for H63D.

Lucotte G, Champenois T, Sémonin O.

Blood Cells Mol Dis. 2001 Sep-Oct;27(5):892-3.PMID: 11783952 [PubMed - indexed for MEDLINE]Related articles

Hemochromatosis: genetics and pathophysiology.

Beutler E.

Annu Rev Med. 2006;57:331-47. Review.PMID: 16409153 [PubMed - indexed for MEDLINE]Related articles

[Hereditary hemochromatosis: molecular diagnosis and effect of treatment]

Szczeklik W, Dropiński J, Dziedzina S, Szułdrzyński K, Biesiada G, Mach T, Sanak M.

Pol Arch Med Wewn. 2004 May;111(5):593-6. Polish. PMID: 15508811 [PubMed - indexed for MEDLINE]Related articles

Hemochromatosis-associated gene mutations in patients with myelodysplastic syndromes with refractory anemia with ringed sideroblasts.

Nearman ZP, Szpurka H, Serio B, Warshawksy I, Theil K, Lichtin A, Sekeres MA, Maciejewski JP.

Am J Hematol. 2007 Dec;82(12):1076-9.PMID: 17654685 [PubMed - indexed for MEDLINE]Related articles

Role of hemochromatosis genes in chronic hepatitis C.

Gattoni A, Parlato A, Vangieri B, Bresciani M, Derna R, Baldassarre R.

Clin Ter. 2006 Jan-Feb;157(1):61-8. Review.PMID: 16669553 [PubMed - indexed for MEDLINE]Related articles

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 [PubMed - indexed for MEDLINE]Related articles

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 [PubMed - indexed for MEDLINE]Related articles

Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.

Simsek H, Balaban YH, Yilmaz E, Sumer H, Buyukasik Y, Cengiz C, Ozcebe O, Hascelik G, Tatar G.

Ann Hematol. 2005 Oct;84(10):646-9. Epub 2005 May 4.PMID: 15871018 [PubMed - indexed for MEDLINE]Related articles

T-cell receptor repertoire in hereditary hemochromatosis: a study of 32 hemochromatosis patients and 274 healthy subjects.

Cardoso C, Porto G, Lacerda R, Resende D, Rodrigues P, Bravo F, Oliveira JC, Justiça B, de Sousa M.

Hum Immunol. 2001 May;62(5):488-99.PMID: 11334672 [PubMed - indexed for MEDLINE]Related articles