141 related articles for article (PubMed ID: 33457423)
21. 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; 130(12):953-62. PubMed ID: 10383365
[TBL] [Abstract][Full Text] [Related]
22. 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. PubMed ID: 14740507
[TBL] [Abstract][Full Text] [Related]
23. HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women.
Warne CD; Zaloumis SG; Bertalli NA; Delatycki MB; Nicoll AJ; McLaren CE; Hopper JL; Giles GG; Anderson GJ; Olynyk JK; Powell LW; Allen KJ; Gurrin LC;
J Gastroenterol Hepatol; 2017 Apr; 32(4):797-802. PubMed ID: 27784128
[TBL] [Abstract][Full Text] [Related]
24. Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population.
Sassi R; Hmida S; Kaabi H; Hajjej A; Abid A; Abdelkefi S; Yacoub S; Maamar M; Mojaat N; Ben Hamed L; Bellali H; Dridi A; Jridi A; Midouni B; Boukef MK
Ann Genet; 2004; 47(4):325-30. PubMed ID: 15581829
[TBL] [Abstract][Full Text] [Related]
25. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population.
Leone PE; Giménez P; Collantes JC; Paz-y-Miño C
Ann Hematol; 2005 Feb; 84(2):103-5. PubMed ID: 15517265
[TBL] [Abstract][Full Text] [Related]
26. 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. PubMed ID: 14675248
[TBL] [Abstract][Full Text] [Related]
27. Transient elevation of serum ferritin in a Sri Lankan with homozygosity for H63D mutation in the HFE gene: a case report.
Wickramasinghe W; Karunathilaka C; Jayasinghe S; Gooneratne L
J Med Case Rep; 2020 Jul; 14(1):93. PubMed ID: 32641120
[TBL] [Abstract][Full Text] [Related]
28. Differential HFE allele expression in hemochromatosis heterozygotes.
Rosmorduc O; Poupon R; Nion I; Wendum D; Feder J; Béréziat G; Hermelin B
Gastroenterology; 2000 Oct; 119(4):1075-86. PubMed ID: 11040194
[TBL] [Abstract][Full Text] [Related]
29. Hereditary hemochromatosis in north-eastern Romania.
Voicu PM; Cojocariu C; Petrescu-Dănilă E; Stanciu C; Covic M; Rusu M; Trifan A
Rev Med Chir Soc Med Nat Iasi; 2010; 114(4):982-7. PubMed ID: 21495455
[TBL] [Abstract][Full Text] [Related]
30. Hereditary hemochromatosis in Spain.
Sánchez M; Bruguera M; Quintero E; Barrio Y; Mazzara R; Rodés J; Oliva R
Genet Test; 2000; 4(2):171-6. PubMed ID: 10953957
[TBL] [Abstract][Full Text] [Related]
31. High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy.
De Marco F; Liguori R; Giardina MG; D'Armiento M; Angelucci E; Lucariello A; Morante R; Cimino L; Galeota-Lanza A; Tarantino G; Ascione A; Budillon G; Vecchione R; Martinelli R; Matarazzo M; De Simone V
Clin Chem Lab Med; 2004 Jan; 42(1):17-24. PubMed ID: 15061375
[TBL] [Abstract][Full Text] [Related]
32. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
Spínola C; Brehm A; Spínola H
Ann Hematol; 2011 Jan; 90(1):29-32. PubMed ID: 20714725
[TBL] [Abstract][Full Text] [Related]
33. Association of HFE gene C282Y and H63D mutations with liver cirrhosis in the Lithuanian population.
Juzėnas S; Kupčinskas J; Valantienė I; Šumskienė J; Petrenkienė V; Kondrackienė J; Kučinskas L; Kiudelis G; Skiecevičienė J; Kupčinskas L
Medicina (Kaunas); 2016; 52(5):269-275. PubMed ID: 27816425
[TBL] [Abstract][Full Text] [Related]
34. Hereditary hemochromatosis: detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic.
Cimburova M; Putova I; Provaznikova H; Horak J
Genet Epidemiol; 2002 Oct; 23(3):260-3. PubMed ID: 12384978
[TBL] [Abstract][Full Text] [Related]
35. An improved real time PCR method for simultaneous detection of C282Y and H63D mutations in the HFE gene associated with hereditary hemochromatosis.
Walburger DK; Afonina IA; Wydro R
Mutat Res; 2001 Jan; 432(3-4):69-78. PubMed ID: 11465544
[TBL] [Abstract][Full Text] [Related]
36. [The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene].
Drastíková M; Beránek M; Hegerová J; Putzová D
Cas Lek Cesk; 2012; 151(9):428-31. PubMed ID: 23102134
[TBL] [Abstract][Full Text] [Related]
37. 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; 341(10):718-24. PubMed ID: 10471457
[TBL] [Abstract][Full Text] [Related]
38. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
[TBL] [Abstract][Full Text] [Related]
39. 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; 25(3-4):147-55. PubMed ID: 10575540
[TBL] [Abstract][Full Text] [Related]
40. An unusual melting curve profile in LightCycler multiplex genotyping of the hemochromatosis H63D/C282Y gene mutations.
Tag CG; Gressner AM; Weiskirchen R
Clin Biochem; 2001 Sep; 34(6):511-5. PubMed ID: 11676983
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]