Publications
Found 3 results
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“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.
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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.
http://dx.doi.org/10.1006/bcmd.1999.0260
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.
http://dx.doi.org/10.1590/S1516-84842007000200017
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.
http://dx.doi.org/10.1590/S0100-879X2002000300007
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.
http://dx.doi.org/10.1590/S1516-84842007000400003
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.
http://dx.doi.org/10.1046/j.1525-1381.1999.99235.x
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.
http://dx.doi.org/10.1086/301878
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.
http://dx.doi.org/10.1590/S0004-28032001000300010
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.
http://dx.doi.org/10.1590/S1516-84842008000500010
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.
http://dx.doi.org/10.1152/ajpgi.00486.2005
PMid:16537971
Frenette PS and Atweh GF (2007). Sickle cell disease: old discoveries, new concepts, and future promise. J. Clin. Invest. 117: 850-858.
http://dx.doi.org/10.1172/JCI30920
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.
http://dx.doi.org/10.1002/ajh.10426
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.
http://dx.doi.org/10.1590/S1676-24442004000400007
Parra FC, Amado RC and Lambertucci JR (2003). Color and genomic ancestry in Brazilians. PNAS 100: 177-182.
http://dx.doi.org/10.1073/pnas.0126614100
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.
http://dx.doi.org/10.1016/j.bbamcr.2006.05.013
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.
http://dx.doi.org/10.1016/S0891-5849(98)00315-3
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.
http://dx.doi.org/10.4238/vol7-1gmr408
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
“Lipid peroxidation and antioxidant capacity of G6PD-deficient patients with A-(202G>A) mutation”, vol. 8, pp. 1345-1351, 2009.
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