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2011
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.
Alter BP, Goff SC, Efremov GD, Gravely ME, et al. (1980). Globin chain electrophoresis: a new approach to the determination of the G gamma/A gamma ratio in fetal haemoglobin and to studies of globin synthesis. Br. J. Haematol. 44: 527-534. http://dx.doi.org/10.1111/j.1365-2141.1980.tb08706.x PMid:6155135 Bonini-Domingos CR (2006). Metodologias Laboratoriais para o Diagnóstico de Hemoglobinopatias e Talassemia. 1ª ed. HN Press, São José do Rio Preto. Craig JE, Barnetson RA, Prior J, Raven JL, et al. (1994). Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification. Blood 83: 1673-1682. PMid:7510147 Forget BG (1998). Molecular basis of hereditary persistence of fetal hemoglobin. Ann. N. Y. Acad. Sci. 850: 38-44. http://dx.doi.org/10.1111/j.1749-6632.1998.tb10460.x PMid:9668525 Galanello R and Cao A (1998). Relationship between genotype and phenotype. Thalassemia intermedia. Ann. N. Y. Acad. Sci. 850: 325-333. http://dx.doi.org/10.1111/j.1749-6632.1998.tb10489.x PMid:9668554 Gibney GT, Panhuysen CI, So JC, Ma ES, et al. (2008). Variation and heritability of Hb F and F-cells among beta-thalassemia heterozygotes in Hong Kong. Am. J. Hematol. 83: 458-464. http://dx.doi.org/10.1002/ajh.21150 PMid:18266208 Grosso M, Amendolara M, Rescigno G, Danise P, et al. (2008). Delayed decline of gamma-globin expression in infant age associated with the presence of Ggamma-158 (C→T) polymorphism. Int. J. Lab. Hematol. 30: 191-195. http://dx.doi.org/10.1111/j.1751-553X.2007.00946.x PMid:18479296 Hoyer JD, Penz CS, Fairbanks VF, Hanson CA, et al. (2002). Flow cytometric measurement of hemoglobin F in RBCs: diagnostic usefulness in the distinction of hereditary persistence of fetal hemoglobin (HPFH) and hemoglobin S-hPFH from other conditions with elevated levels of hemoglobin F. Am. J. Clin. Pathol. 117: 857-863. http://dx.doi.org/10.1309/A63X-HG9T-VYG2-X6TX PMid:12047136 Huisman HJ, Carver MFH, Baysal E and Efremov GD (1996). HbVar: A Database of Human Hemoglobin Variants and Thalassemias. Summaries of Mutation Categories. Pennsylvania University USA and McMaster University in Canada. Available at [http://globin.cse.psu.edu/]. Accessed April 26, 2010. Marengo-Rowe AJ (1965). Rapid electrophoresis and quantitation of haemoglobins on cellulose acetate. J. Clin. Pathol. 18: 790-792. http://dx.doi.org/10.1136/jcp.18.6.790 PMid:5844210    PMCid:473136 Nussbaum RL, McInnes RR and Willard HF (2008). Thompson & Thompson: Genética Médica. 7ª ed. Elsevier Press, Rio de Janeiro. Old JM (2003). Screening and genetic diagnosis of haemoglobin disorders. Blood Rev. 17: 43-53. http://dx.doi.org/10.1016/S0268-960X(02)00061-9 Pena SD, Macedo AM, Gontijo NF, Medeiros AM, et al. (1991). DNA bioprints: simple nonisotopic DNA fingerprints with biotinylated probes. Electrophoresis 12: 146-152. http://dx.doi.org/10.1002/elps.1150120209 PMid:2040262 Pena SD, Carvalho-Silva DR, Alves-Silva J and Prado VF (2000). Retrato molecular do Brasil. Ciênc. Hoje 27: 16-25. Silvestroni E and Bianco I (1975). Screening for microcytemia in Italy: analysis of data collected in the past 30 years. Am. J. Hum. Genet. 27: 198-212. PMid:1124764    PMCid:1762748 Stamatoyannopoulos G and Nienhuis AW (1994). Hemoglobin Switching. In: The Molecular Basis of Blood Diseases. 2nd edn. (Stamatoyannopoulos G, Nienhuis AW, Majerus PW and Varmus H, eds.). WB Saunders Company Press, Philadelphia, 107-155. Steinberg MH (2009). Genetic etiologies for phenotypic diversity in sickle cell anemia. Sci. World J. 9: 46-67. http://dx.doi.org/10.1100/tsw.2009.10 PMid:19151898 Thein SL (2005). Genetic modifiers of beta-thalassemia. Haematologica 90: 649-660. PMid:15921380 Vella F (1968). Acid-agar gel electrophoresis of human hemoglobins. Am. J. Clin. Pathol. 49: 440-442. PMid:5645100 Vives-Corrons JL, Pujades MA and Miguel A (1991). Screening of Spanish (δβ0) thalassemia by polimerase chain reaction (PCR). Combined Meeting of British Society for Haematology and British Society for Haemostasis and Thrombosis, Glasgow, March 20-22, 1991, Abstracts. Br. J. Haematol. 77 (Suppl 1): 1-84. Weatherall DJ (2001). Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias. Nat. Rev. Genet. 2: 245-255. http://dx.doi.org/10.1038/35066048 PMid:11283697 Weatherall DJ and Clegg JB (2001). The Thalassemia Syndromes. 4th edn. Oxford Blackwell Science, England. http://dx.doi.org/10.1002/9780470696705 Zago MA, Falcão RP and Pasquini R (2004). Hematologia: Fundamentos e Prática. 1ª ed. Ateneu Press, São Paulo.
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.
Alter BP, Goff SC, Efremov GD, Gravely ME, et al. (1980). Globin chain electrophoresis: a new approach to the determination of the G gamma/A gamma ratio in fetal haemoglobin and to studies of globin synthesis. Br. J. Haematol. 44: 527-534. http://dx.doi.org/10.1111/j.1365-2141.1980.tb08706.x PMid:6155135   Bonini-Domingos CR (2006). Metodologias Laboratoriais para o Diagnóstico de Hemoglobinopatias e Talassemias. Editora HN, São José do Rio Preto.   Bunn HF and Forget BG (1986). Hemoglobin: Molecular Genetic and Clinical Aspects. Saunders, Philadelphia.   Clark BE and Thein SL (2004). Molecular diagnosis of haemoglobin disorders. Clin. Lab. Haematol. 26: 159-176. http://dx.doi.org/10.1111/j.1365-2257.2004.00607.x PMid:15163314   Dacie JV and Lewis SM (1985). Practical Haematology. 6th edn. Churchill, London.   Eastman JW, Wong R, Liao CL and Morales DR (1996). Automated HPLC screening of newborns for sickle cell anemia and other hemoglobinopathies. Clin. Chem. 42: 704-710. PMid:8653895   Huisman HJ, Carver MFH and Efremov GD (2009). HbVar: A Database of Human Hemoglobin Variants and Thalassemias. Summaries and Mutation Categories. Pennsylvania University USA, and McMaster University, Canada. Available at [http://globin.bx.psu.edu/hbvar/menu.html]. Accessed May 2009.   Lehmann H and Huntsman RG (1974). Man's Haemoglobins. North Holland Publishing Company, Amsterdam.   Leoneli GG (2001). Hemoglobina D - Caracterização Eletroforética e Molecular. Master's thesis, Instituto de Biociências, Letras e Ciências Exatas, Universidade Estadual Paulista, São José do Rio Preto.   Marengo-Rowe AJ (1965). Rapid electrophoresis and quantitation of haemoglobins on cellulose acetate. J. Clin. Pathol. 18: 790-792. http://dx.doi.org/10.1136/jcp.18.6.790 PMid:5844210 PMCid:473136   Papayannopoulos R and Stamatoyannopoulos G (1974). Stains for Inclusion Bodies. In: Standardization of Laboratory Reagents and Methodos for Detection of Haemoglobinopathies. Hew publications, Atlanta, 174-178.   Pena SD, Macedo AM, Gontijo NF, Medeiros AM, et al. (1991). DNA bioprints: simple nonisotopic DNA fingerprints with biotinylated probes. Electrophoresis 12: 146-152. http://dx.doi.org/10.1002/elps.1150120209 PMid:2040262   Schneider RG (1974). Differentiation of electrophoretically similar hemoglobins - such as S, D, G, and P; or A2, C, E, and O - by electrophoresis of the globin chains. Clin. Chem. 20: 1111-1115. PMid:4412820   Silvestroni E and Bianco I (1975). Screening for microcytemia in Italy: analysis of data collected in the past 30 years. Am. J. Hum. Genet. 27: 198-212. PMid:1124764 PMCid:1762748   Vella F (1968). Acid-agar gel electrophoresis of human hemoglobins. Am. J. Clin. Pathol. 49: 440-442. PMid:5645100   Zamaro PJA, Canalli AA, Silva Júnior WA and Bonini-Domingos CR (2002). Laboratorial diagnosis for hemoglobin like HbS. [Diagnóstico laboratorial de hemoglobinas semelhantes à HbS]. J. Bras. Patol. Med. Labor. 38: 261-266. http://dx.doi.org/10.1590/S1676-24442002000400003