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.
264 related articles for article (PubMed ID: 15528154)
1. Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele. Biasiotto G; Roetto A; Daraio F; Polotti A; Gerardi GM; Girelli D; Cremonesi L; Arosio P; Camaschella C Blood Cells Mol Dis; 2004; 33(3):338-43. PubMed ID: 15528154 [TBL] [Abstract][Full Text] [Related]
2. Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene. Altès A; Bach V; Ruiz A; Esteve A; Felez J; Remacha AF; Sardà MP; Baiget M Ann Hematol; 2009 Oct; 88(10):951-5. PubMed ID: 19214511 [TBL] [Abstract][Full Text] [Related]
3. Identification of new mutations of the HFE, hepcidin, and transferrin receptor 2 genes by denaturing HPLC analysis of individuals with biochemical indications of iron overload. Biasiotto G; Belloli S; Ruggeri G; Zanella I; Gerardi G; Corrado M; Gobbi E; Albertini A; Arosio P Clin Chem; 2003 Dec; 49(12):1981-8. PubMed ID: 14633868 [TBL] [Abstract][Full Text] [Related]
4. Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis. Merryweather-Clarke AT; Cadet E; Bomford A; Capron D; Viprakasit V; Miller A; McHugh PJ; Chapman RW; Pointon JJ; Wimhurst VL; Livesey KJ; Tanphaichitr V; Rochette J; Robson KJ Hum Mol Genet; 2003 Sep; 12(17):2241-7. PubMed ID: 12915468 [TBL] [Abstract][Full Text] [Related]
5. [Pathophysiology and genetics of classic HFE (type 1) hemochromatosis]. Loréal O; Ropert M; Mosser A; Déhais V; Deugnier Y; David V; Brissot P; Jouanolle AM Presse Med; 2007 Sep; 36(9 Pt 2):1271-7. PubMed ID: 17521857 [TBL] [Abstract][Full Text] [Related]
6. Hemochromatosis: genetics and pathophysiology. Beutler E Annu Rev Med; 2006; 57():331-47. PubMed ID: 16409153 [TBL] [Abstract][Full Text] [Related]
7. Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain. de Diego C; Murga MJ; Martínez-Castro P Genet Test; 2004; 8(3):263-7. PubMed ID: 15727249 [TBL] [Abstract][Full Text] [Related]
9. Blunted hepcidin response to oral iron challenge in HFE-related hemochromatosis. Piperno A; Girelli D; Nemeth E; Trombini P; Bozzini C; Poggiali E; Phung Y; Ganz T; Camaschella C Blood; 2007 Dec; 110(12):4096-100. PubMed ID: 17724144 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. HFE, hepcidin and ferroportin gene mutations are not present in Indian patients with primary haemochromatosis. Shukla P; Julka S; Bhatia E; Shah S; Nagral A; Aggarwal R Natl Med J India; 2006; 19(1):20-3. PubMed ID: 16570681 [TBL] [Abstract][Full Text] [Related]
12. Prevalence of hemochromatosis gene (HFE) mutations in Greece. Papazoglou D; Exiara T; Speletas M; Panagopoulos I; Maltezos E Acta Haematol; 2003; 109(3):137-40. PubMed ID: 12714823 [TBL] [Abstract][Full Text] [Related]
13. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis. Bittencourt PL; Palácios SA; Couto CA; Cançado EL; Carrilho FJ; Laudanna AA; Kalil J; Gayotto LC; Goldberg AC Braz J Med Biol Res; 2002 Mar; 35(3):329-35. PubMed ID: 11887210 [TBL] [Abstract][Full Text] [Related]
14. HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype. Jacolot S; Le Gac G; Scotet V; Quere I; Mura C; Ferec C Blood; 2004 Apr; 103(7):2835-40. PubMed ID: 14670915 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants. Barton JC; Lafreniere SA; Leiendecker-Foster C; Li H; Acton RT; Press RD; Eckfeldt JH Am J Hematol; 2009 Nov; 84(11):710-4. PubMed ID: 19787796 [TBL] [Abstract][Full Text] [Related]
17. A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote. Wallace DF; Dooley JS; Walker AP Gastroenterology; 1999 Jun; 116(6):1409-12. PubMed ID: 10348824 [TBL] [Abstract][Full Text] [Related]
18. A time course of hepcidin response to iron challenge in patients with HFE and TFR2 hemochromatosis. Girelli D; Trombini P; Busti F; Campostrini N; Sandri M; Pelucchi S; Westerman M; Ganz T; Nemeth E; Piperno A; Camaschella C Haematologica; 2011 Apr; 96(4):500-6. PubMed ID: 21173098 [TBL] [Abstract][Full Text] [Related]