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L. M. S. Viana-Baracioli, Junior, N. C. Tukamoto, O. Júnior, R., Mattos, L. C., Ângulo, I. L., and Bonini-Domingos, C. R., Comparison of oxidative stress and the frequency of polymorphisms in the HFE gene between hemoglobin S trait blood donors and sickle cell disease patients, vol. 10, pp. 3446-3454, 2011.
Agostinho MF, Arruda VR, Basseres DS, Bordin S, et al. (1999). Mutation analysis of the HFE gene in Brazilian populations. Blood Cells Mol. Dis. 25: 324-327. PMid:10660479   Bandeira FMGC, Bezerra MAC, Santos MNN and Gomes YM (2007). Importância dos programas de triagem para o gene da hemoglobina S. Rev. Bras. Hematol. Hemoter. 29: 179-184.   Beutler E (2004). Iron absorption in carriers of the C282Y hemochromatosis mutation. Am. J. Clin. Nutr. 80: 799-800. PMid:15447883   Beutler E, Lichtman MA, Coller BS and Kipps TJ (1995). Williams Hematology. 5th edn. International Edition, New York.   Bittencourt PL, Palacios SA, Couto CA, Cancado EL, et al. (2002). Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis. Braz. J. Med. Biol. Res. 35: 329-335. PMid:11887210   Bonini-Domingos CR (2007). Aumento de ferro, hemocromatose hereditária e defeitos no gene HFE. O que conhecemos na população brasileira? Rev. Bras. Hematol. Hemoter. 29: 341-342.   Bonini-Domingos CR, Ondei LS and Zamaro PJA (2006). Hemoglobinas Similares a S no Brasil - Um Guia Prático de Identificação. 1ª ed. Editora HN, São José do Rio Preto.   Clegg JB and Weatherall DJ (1999). Thalassemia and malaria: new insights into an old problem. Proc. Assoc. Am. Physicians 111: 278-282. PMid:10417734   Cullen LM, Gao X, Easteal S and Jazwinska EC (1998). The hemochromatosis 845 G→A and 187 C→G mutations: prevalence in non-Caucasian populations. Am. J. Hum. Genet. 62: 1403-1407. PMid:9585606 PMCid:1377157   de Souza AF, Carvalho-Filho RJ and Chebli JF (2001). Hereditary hemochromatosis. Case report and review of the literature. Arq. Gastroenterol. 38: 194-202. PMid:11917720   Ferreira ACS, Oliveira VC, Caxito FA and Gomes KB (2008). Prevalence of C282Y and H63D mutations in the gene of Brazilian individuals with clinical suspicion of hereditary hemochromatosis. Rev. Bras. Hematol. Hemoter. 30: 379-383.   Fleming RE and Britton RS (2006). Iron Imports. VI. HFE and regulation of intestinal iron absorption. Am. J. Physiol. Gastrointest. Liver Physiol. 290: G590-G594. PMid:16537971   Frenette PS and Atweh GF (2007). Sickle cell disease: old discoveries, new concepts, and future promise. J. Clin. Invest. 117: 850-858. PMid:17404610 PMCid:1838946   Higgs DR and Weatherall DJ (1993). Thalassaemia. In: The Haemoglobinopathies (WB Saunders, ed.). Baillière's Clinical Hematology, London, 117.   Jeng MR, Adams-Graves P, Howard TA, Whorton MR, et al. (2003). Identification of hemochromatosis gene polymorphisms in chronically transfused patients with sickle cell disease. Am. J. Hematol. 74: 243-248. PMid:14635204   Naoum PC and Souza PC (2004). Avaliação dos produtos da degradação oxidativa da Hb S nos genótipos SS, SF (S/beta 0 talassemia) e AS, em comparação com hemoglobinas normais. Rev. Bras. Patol. Med. Lab. 40: 249-259.   Parra FC, Amado RC and Lambertucci JR (2003). Color and genomic ancestry in Brazilians. PNAS 100: 177-182. PMid:12509516 PMCid:140919   Percário S (1999). Dosagem do Dialdeido Malônico. NEWSLAB, 46-50.   Pietrangelo A (2006). Hereditary hemochromatosis. Biochim. Biophys. Acta 1763: 700-710. PMid:16891003   Powell LW (2002). Diagnosis of hemochromatosis. Semin. Gastrointest. Dis. 13: 80-88. PMid:12064863   Re R, Pellegrini N, Proteggente A, Pannala A, et al. (1999). Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radic. Biol. Med. 26: 1231-1237.   Serjeant GR (1992). Sickle Cell Disease. 2nd edn. Oxford University Press Inc., New York.   Siah CW, Ombiga J, Adams LA, Trinder D, et al. (2006). Normal iron metabolism and the pathophysiology of iron overload disorders. Clin. Biochem. Rev. 27: 5-16. PMid:16886043 PMCid:1390789   Torres FR, Souza-Neiras WC, D'Almeida Couto AA, D'Almeida Couto VS, et al. (2008). Frequency of the HFE C282Y and H63D polymorphisms in Brazilian malaria patients and blood donors from the Amazon region. Genet. Mol. Res. 7: 60-64. PMid:18273820   Weatherall DJ and Clegg JB (2001). Inherited haemoglobin disorders: an increasing global health problem. Bull World Health Organ 79: 704-712. PMid:11545326 PMCid:2566499