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2011
I. F. Estevão, P. Junior, P., and Bonini-Domingos, C. R., Serum ferritin and transferrin saturation levels in β0 and β+ thalassemia patients, vol. 10, pp. 632-639, 2011.
Aranda N, Viteri FE, Montserrat C and Arija V (2010). 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. Ann. Hematol. 89: 767-773. doi:10.1007/s00277-010-0901-9 Bertholo LC and Moreira HW (2006). Amplificação gênica alelo-específica na caracterização das hemoglobinas S, C e D e as interações entre elas e talassemias beta. J. Bras. Patol. Med. Lab. 42: 245-251. Brissot P, Troadec MB, Bardou-Jacquet E, Le Lan C, et al. (2008). Current approach to hemochromatosis. Blood Rev. 22: 195-210. doi:10.1016/j.blre.2008.03.001 Camaschella C (2005). Understanding iron homeostasis through genetic analysis of hemochromatosis and related disorders. Blood 106: 3710-3717. doi:10.1182/blood-2005-05-1857 Camaschella C and Poggiali E (2009). Towards explaining “unexplained hyperferritinemia”. Haematologica 94: 307-309. doi:10.3324/haematol.2008.005405 Cassanelli S, Pignatti E, Montosi G, Garuti C, et al. (2001). Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy. J. Hepatol. 34: 523-528. doi:10.1016/S0168-8278(01)00035-6 Demir A, Yarali N, Fisgin T, Duru F, et al. (2004). Serum transferrin receptor levels in beta-thalassemia trait. J. Trop. Pediatr. 50: 369-371. doi:10.1093/tropej/50.6.369 Edwards CQ, Skolnick MH and Kushner JP (1981). Coincidental nontransfusional iron overload and thalassemia minor: association with HLA-linked hemochromatosis. Blood 58: 844-848. Fargion S, Taddei MT, Cappellini MD, Piperno A, et al. (1982). The iron status of Italian subjects with beta-thalassemia trait. Acta Haematol. 68: 109-114. doi:10.1159/000206961 Fargion S, Piperno A, Panaiotopoulos N, Taddei MT, et al. (1985). Iron overload in subjects with beta-thalassaemia trait: role of idiopathic haemochromatosis gene. Br. J. Haematol. 61: 487-490. doi:10.1111/j.1365-2141.1985.tb02852.x Garcia PJ, Moreu AI, Asensio MA and Rueda GA (1993). Disease caused by iron overload associated to minor beta thalassemia. An. Med. Intern. 10: 203. Girouard J, Giguere Y, Delage R and Rousseau F (2002). Prevalence of HFE gene C282Y and H63D mutations in a French-Canadian population of neonates and in referred patients. Hum. Mol. Genet. 11: 185-189. doi:10.1093/hmg/11.2.185 Gordeuk VR, Reboussin DM, McLaren CE, Barton JC, et al. (2008). Serum ferritin concentrations and body iron stores in a multicenter, multiethnic primary-care population. Am. J. Hematol. 83: 618-626. doi:10.1002/ajh.21179 Kannengiesser C, Jouanolle AM, Hetet G, Mosser A, et al. (2009). A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload. Haematologica 94: 335-339. doi:10.3324/haematol.2008.000125 Lewis M, Lee GR and Haut A (1965). The association of hemochromatosis with thalassemia minor. Ann. Intern. Med. 63: 122-128. Lynas C (1997). A cheaper and more rapid polymerase chain reaction-restriction fragment length polymorphism method for the detection of the HLA-H gene mutations occurring in hereditary hemochromatosis. Blood 90: 4235-4236. Martins R, Picanco I, Fonseca A, Ferreira L, et al. (2004). The role of HFE mutations on iron metabolism in beta-thalassemia carriers. J. Hum. Genet. 49: 651-655. doi:10.1007/s10038-004-0202-z Melchiori L, Gardenghi S and Rivella S (2010). Beta-Thalassemia: HiJAKing ineffective erythropoiesis and iron overload. Adv. Hematol. 2010: 938640. doi:10.1155/2010/938640 Melis MA, Cau M, Deidda F, Barella S, et al. (2002). H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers. Haematologica 87: 242-245. Miniero R, Tardivo I, Roetto A and De Gobbi M (2005). Heterozygous beta-thalassemia and homozygous H63D hemochromatosis in a child: an 18-year follow-up. Pediatr. Hematol. Oncol. 22: 163-166. doi:10.1080/08880010590907302 Parfrey PS, Barnett M, Sachs JA, Pollock DJ, et al. (1981). Iron overload in beta-thalassaemia minor. A family study. Scand. J. Haematol. 27: 294-302. doi:10.1111/j.1600-0609.1981.tb00487.x Piperno A, Mariani R, Arosio C, Vergani A, et al. (2000). Haemochromatosis in patients with beta-thalassaemia trait. Br. J. Haematol. 111: 908-914. doi:10.1046/j.1365-2141.2000.02436.x Restagno G, Gomez AM, Sbaiz L, De Gobbi M, et al. (2000). A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technology. Genet. Test. 4: 177-181. doi:10.1089/10906570050114894 Weatherall DJ (2007). Current trends in the diagnosis and management of haemoglobinopathies. Scand. J. Clin. Lab. Invest. 67: 1-2. doi:10.1080/00365510601051532 Yen AW, Fancher TL and Bowlus CL (2006). Revisiting hereditary hemochromatosis: current concepts and progress. Am. J. Med. 119: 391-399. doi:10.1016/j.amjmed.2005.10.041