These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
95 related articles for article (PubMed ID: 28727322)
1. HFE gene polymorphism defined by sequence-based typing of the Brazilian population and a standardized nomenclature for HFE allele sequences. Campos WN; Massaro JD; Martinelli ALC; Halliwell JA; Marsh SGE; Mendes-Junior CT; Donadi EA HLA; 2017 Oct; 90(4):238-242. PubMed ID: 28727322 [TBL] [Abstract][Full Text] [Related]
2. 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; 27(1):290-3. PubMed ID: 11358390 [TBL] [Abstract][Full Text] [Related]
3. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population. Kucinskas L; Juzenas S; Sventoraityte J; Cedaviciute R; Vitkauskiene A; Kalibatas V; Kondrackiene J; Kupcinskas L Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086 [TBL] [Abstract][Full Text] [Related]
4. Comprehensive analysis of de Campos WN; Massaro JD; Cançado ELR; Wiezel CEV; Simões AL; Teixeira AC; de Souza FF; Mendes-Junior CT; Martinelli ALC; Donadi EA World J Hepatol; 2019 Feb; 11(2):186-198. PubMed ID: 30820268 [TBL] [Abstract][Full Text] [Related]
6. Carriers of the Complex Allele HFE c.[187C>G;340+4T>C] Have Increased Risk of Iron Overload in São Miguel Island Population (Azores, Portugal). Branco CC; Gomes CT; De Fez L; Bulhões S; Brilhante MJ; Pereirinha T; Cabral R; Rego AC; Fraga C; Miguel AG; Brasil G; Macedo P; Mota-Vieira L PLoS One; 2015; 10(10):e0140228. PubMed ID: 26501199 [TBL] [Abstract][Full Text] [Related]
7. Polymorphisms in the HFE gene. Douabin V; Moirand R; Jouanolle A; Brissot P; Le Gall J; Deugnier Y; David V Hum Hered; 1999 Jan; 49(1):21-6. PubMed ID: 9858853 [TBL] [Abstract][Full Text] [Related]
8. Haplotype analysis of the H63D, IVS2+4t/c, and C282Y polymorphisms of the HFE gene reveals rare events of intragenic recombination. Curcio M; Fornaciari S; Mariotti ML; Chelazzi S; Scatena F; Presciuttini S Eur J Haematol; 2008 Apr; 80(4):341-5. PubMed ID: 18182079 [TBL] [Abstract][Full Text] [Related]
9. 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; 4(1):31-8. PubMed ID: 15841433 [TBL] [Abstract][Full Text] [Related]
10. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms. Lee PL; Gelbart T; West C; Halloran C; Beutler E Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100 [TBL] [Abstract][Full Text] [Related]
11. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload. Barton JC; Wiener HW; Acton RT; Go RC Blood Cells Mol Dis; 2005; 34(1):38-47. PubMed ID: 15607698 [TBL] [Abstract][Full Text] [Related]
12. Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis. Hamdi-Rozé H; Beaumont-Epinette MP; Ben Ali Z; Le Lan C; Loustaud-Ratti V; Causse X; Loreal O; Deugnier Y; Brissot P; Jouanolle AM; Bardou-Jacquet E Am J Hematol; 2016 Dec; 91(12):1202-1205. PubMed ID: 27518069 [TBL] [Abstract][Full Text] [Related]
13. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study. Adams PC; Pankow JS; Barton JC; Acton RT; Leiendecker-Foster C; McLaren GD; Speechley M; Eckfeldt JH Circ Cardiovasc Genet; 2009 Feb; 2(1):34-7. PubMed ID: 20031565 [TBL] [Abstract][Full Text] [Related]
14. The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene. Silva B; Pita L; Gomes S; Gonçalves J; Faustino P Ann Hematol; 2014 Dec; 93(12):2063-6. PubMed ID: 25015054 [TBL] [Abstract][Full Text] [Related]
15. The influence of hemochromatosis mutations on iron overload of thalassemia major. Longo F; Zecchina G; Sbaiz L; Fischer R; Piga A; Camaschella C Haematologica; 1999 Sep; 84(9):799-803. PubMed ID: 10477452 [TBL] [Abstract][Full Text] [Related]
16. Prevalence and clinical significance of HFE gene mutations in patients with iron overload. Brandhagen DJ; Fairbanks VF; Baldus WP; Smith CI; Kruckeberg KE; Schaid DJ; Thibodeau SN Am J Gastroenterol; 2000 Oct; 95(10):2910-4. PubMed ID: 11051367 [TBL] [Abstract][Full Text] [Related]
17. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing? Santos PC; Pereira AC; Cançado RD; Schettert IT; Sobreira TJ; Oliveira PS; Hirata RD; Hirata MH; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM Blood Cells Mol Dis; 2010 Dec; 45(4):302-7. PubMed ID: 20843714 [TBL] [Abstract][Full Text] [Related]
18. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda. Gonzalez-Hevilla M; de Salamanca RE; Morales P; Martínez-Laso J; Fontanellas A; Castro MJ; Rojo R; Moscoso J; Zamora J; Serrano-Vela JI; Arnaiz-Villena A J Gastroenterol Hepatol; 2005 Mar; 20(3):456-62. PubMed ID: 15740492 [TBL] [Abstract][Full Text] [Related]
19. - 174 G>C IL-6 polymorphism and primary iron overload in male patients. Tetzlaff WF; Meroño T; Botta EE; Martín ME; Sorroche PB; Boero LE; Castro M; Frechtel GD; Rey J; Daruich J; Cerrone GE; Brites F Ann Hematol; 2018 Sep; 97(9):1683-1687. PubMed ID: 29656314 [TBL] [Abstract][Full Text] [Related]
20. Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder. Viprakasit V; Vathesathokit P; Chinchang W; Tachavanich K; Pung-Amritt P; Wimhurst VL; Yenchitsomanus PT; Merryweather-Clarke AT; Tanphaichitr VS Eur J Haematol; 2004 Jul; 73(1):43-9. PubMed ID: 15182337 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]