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2016
G. S. Martins, Alevi, K. C. C., Azeredo-Oliveira, M. T. V., Bonini-Domingos, C. R., Martins, G. S., Alevi, K. C. C., Azeredo-Oliveira, M. T. V., Bonini-Domingos, C. R., Martins, G. S., Alevi, K. C. C., Azeredo-Oliveira, M. T. V., and Bonini-Domingos, C. R., Cytochemical characteristics of blood cells from Brazilian tortoises (Testudines: Testudinidae), vol. 15, p. -, 2016.
G. S. Martins, Alevi, K. C. C., Azeredo-Oliveira, M. T. V., Bonini-Domingos, C. R., Martins, G. S., Alevi, K. C. C., Azeredo-Oliveira, M. T. V., Bonini-Domingos, C. R., Martins, G. S., Alevi, K. C. C., Azeredo-Oliveira, M. T. V., and Bonini-Domingos, C. R., Cytochemical characteristics of blood cells from Brazilian tortoises (Testudines: Testudinidae), vol. 15, p. -, 2016.
G. S. Martins, Alevi, K. C. C., Azeredo-Oliveira, M. T. V., Bonini-Domingos, C. R., Martins, G. S., Alevi, K. C. C., Azeredo-Oliveira, M. T. V., Bonini-Domingos, C. R., Martins, G. S., Alevi, K. C. C., Azeredo-Oliveira, M. T. V., and Bonini-Domingos, C. R., Cytochemical characteristics of blood cells from Brazilian tortoises (Testudines: Testudinidae), vol. 15, p. -, 2016.
J. V. Okumura, Shimauti, E. L. T., Silva, D. G. H., Torres, L. S., Belini-Junior, E., Oliveira, R. G., Patussi, E. V., Herrero, J. C. M., Bonini-Domingos, C. R., Okumura, J. V., Shimauti, E. L. T., Silva, D. G. H., Torres, L. S., Belini-Junior, E., Oliveira, R. G., Patussi, E. V., Herrero, J. C. M., and Bonini-Domingos, C. R., Hemoglobin (Hb) Val de Marne (Hb Footscray) in Brazil: the first case report, vol. 15, p. -, 2016.
J. V. Okumura, Shimauti, E. L. T., Silva, D. G. H., Torres, L. S., Belini-Junior, E., Oliveira, R. G., Patussi, E. V., Herrero, J. C. M., Bonini-Domingos, C. R., Okumura, J. V., Shimauti, E. L. T., Silva, D. G. H., Torres, L. S., Belini-Junior, E., Oliveira, R. G., Patussi, E. V., Herrero, J. C. M., and Bonini-Domingos, C. R., Hemoglobin (Hb) Val de Marne (Hb Footscray) in Brazil: the first case report, vol. 15, p. -, 2016.
N. R. A. Costa, Venancio, L. P. R., Bonini-Domingos, C. R., Costa, N. R. A., Venancio, L. P. R., and Bonini-Domingos, C. R., Mechanisms of antioxidant defense in the state of post-hypoxia in Phrynops geoffroanus (Testudines: Chelidae), vol. 15, no. 4, p. -, 2016.
ACKNOWLEDGMENTS Research supported by FAPESP (Process #2014/22398-9 and Process #2012/14048-2). Thanks are due to Gabriela de Sousa Martins, Camila Zucchini de Souza, Lucas Ramos Pereira, Dr. Danilo Grünig Humberto da Silva, and Dr. Eduardo Alves de Almeida (UNESP/IBILCE).
N. R. A. Costa, Venancio, L. P. R., Bonini-Domingos, C. R., Costa, N. R. A., Venancio, L. P. R., and Bonini-Domingos, C. R., Mechanisms of antioxidant defense in the state of post-hypoxia in Phrynops geoffroanus (Testudines: Chelidae), vol. 15, no. 4, p. -, 2016.
ACKNOWLEDGMENTS Research supported by FAPESP (Process #2014/22398-9 and Process #2012/14048-2). Thanks are due to Gabriela de Sousa Martins, Camila Zucchini de Souza, Lucas Ramos Pereira, Dr. Danilo Grünig Humberto da Silva, and Dr. Eduardo Alves de Almeida (UNESP/IBILCE).
2011
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. 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
G. C. S. Carrocini, Ondei, L. S., Zamaro, P. J. A., and Bonini-Domingos, C. R., Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels, vol. 10, pp. 3213-3219, 2011.
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G. C. S. Carrocini and Bonini-Domingos, C. R., Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population, vol. 10. pp. 1787-1788, 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
T. L. Silva, Silva, M. I. A., Venancio, L. P. R., Zago, C. E. S., Moscheta, V. A. G., Lima, A. V. B., Vizotto, L. D., Santos, J. R., Bonini-Domingos, C. R., and Azeredo-Oliveira, M. T. V., Simple method for culture of peripheral blood lymphocytes of Testudinidae, vol. 10, pp. 3020-3025, 2011.
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2010
P. J. A. Zamaro and Bonini-Domingos, C. R., Abnormal hemoglobin phenotypes in carriers of mild anemia in Latin America, vol. 9. pp. 425-428, 2010.
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