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310 related items for PubMed ID: 17297430
1. Association of HFE mutations (C282Y and H63D) with iron overload in blood donors from Mexico City. Baptista-González HA, Rosenfeld-Mann F, Trueba-Gómez R, Bermejo-Martínez L, Méndez-Sánchez N. Ann Hepatol; 2007; 6(1):55-60. PubMed ID: 17297430 [Abstract] [Full Text] [Related]
2. HFE mutations, iron deficiency and overload in 10,500 blood donors. Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M. Br J Haematol; 2001 Aug; 114(2):474-84. PubMed ID: 11529872 [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 [Abstract] [Full Text] [Related]
4. Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload. Cançado RD, Guglielmi AC, Vergueiro CS, Rolim EG, Figueiredo MS, Chiattone CS. Sao Paulo Med J; 2006 Mar 02; 124(2):55-60. PubMed ID: 16878186 [Abstract] [Full Text] [Related]
5. [Mutations in the HFE gene (C282Y, H63D, S65C) in alcoholic patients with finding of iron overload]. Campos Franco J, González Quintela A, Fernández de Trocóniz LL, Barros Angueira F, Pérez-Quintela BV, Pérez Becerra E, Martínez de Rituerto ST, Otero Antón E, Torre Carballada JA. Rev Clin Esp; 2002 Oct 02; 202(10):534-9. PubMed ID: 12361551 [Abstract] [Full Text] [Related]
6. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia]. Nie L, Ai XF, Zheng YZ, Li QH, Yang L, Xiao ZJ. Zhonghua Xue Ye Xue Za Zhi; 2009 Apr 02; 30(4):223-8. PubMed ID: 19731820 [Abstract] [Full Text] [Related]
7. 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 02; 73(1):43-9. PubMed ID: 15182337 [Abstract] [Full Text] [Related]
8. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis. Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP. Eur J Immunogenet; 2000 Jun 02; 27(3):129-34. PubMed ID: 10940080 [Abstract] [Full Text] [Related]
9. Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls. Holmström P, Marmur J, Eggertsen G, Gåfvels M, Stål P. Gut; 2002 Nov 02; 51(5):723-30. PubMed ID: 12377814 [Abstract] [Full Text] [Related]
10. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay. Cukjati M, Vaupotic T, Rupreht R, Curin-Serbec V. BMC Med Genet; 2007 Nov 23; 8():69. PubMed ID: 18036208 [Abstract] [Full Text] [Related]
11. An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy. Floreani A, Rosa Rizzotto E, Basso D, Navaglia F, Zaninotto M, Petridis I, DI Andrea O, Testa R, Marra M, Baldo V, Chiaramonte M. Aliment Pharmacol Ther; 2007 Aug 15; 26(4):577-86. PubMed ID: 17661761 [Abstract] [Full Text] [Related]
12. Hemochromatosis and iron-overload screening in a racially diverse population. Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators. N Engl J Med; 2005 Apr 28; 352(17):1769-78. PubMed ID: 15858186 [Abstract] [Full Text] [Related]
13. Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain. Aranda N, Viteri FE, Montserrat C, Arija V. Ann Hematol; 2010 Aug 28; 89(8):767-73. PubMed ID: 20107990 [Abstract] [Full Text] [Related]
14. Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload. De Gobbi M, Daraio F, Oberkanins C, Moritz A, Kury F, Fiorelli G, Camaschella C. Haematologica; 2003 Apr 28; 88(4):396-401. PubMed ID: 12681966 [Abstract] [Full Text] [Related]
15. Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait. Garewal G, Das R, Ahluwalia J, Marwaha RK. Eur J Haematol; 2005 Apr 28; 74(4):333-6. PubMed ID: 15777346 [Abstract] [Full Text] [Related]
16. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes. Raddatz D, Legler T, Lynen R, Addicks N, Ramadori G. Z Gastroenterol; 2003 Nov 28; 41(11):1069-76. PubMed ID: 14648375 [Abstract] [Full Text] [Related]
17. Analysis of HFE-codon 63/282 (H63D/C282Y) gene variants in mexican mestizos. Blood donors and patients with hereditary hemochromatosis. Ruiz-Argüelles GJ, Garcés-Eisele J, Gelbart T, Monroy-Barreto M, Reyes-Núñez V, Juárez-Morales JL, de Lourdes González-Garrido M, Ramírez-Cisneros FJ, Gallegos-Antúnez D. Arch Med Res; 2000 Nov 28; 31(4):422-4. PubMed ID: 11068087 [Abstract] [Full Text] [Related]
18. Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients. Phatak PD, Ryan DH, Cappuccio J, Oakes D, Braggins C, Provenzano K, Eberly S, Sham RL. Blood Cells Mol Dis; 2002 Nov 28; 29(1):41-7. PubMed ID: 12482402 [Abstract] [Full Text] [Related]
20. Frequency of the hemochromatosis gene (HFE) variants in a Jordanian Arab population and in diabetics from the same region. Alkhateeb A, Uzrail A, Bodoor K. Dis Markers; 2009 Nov 28; 27(1):17-22. PubMed ID: 19822954 [Abstract] [Full Text] [Related] Page: [Next] [New Search]