Publications
Found 4 results
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“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.
“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
“Description of electrophoretic and chromatographic hemoglobin profile of Rhinoclemmys punctularia”, vol. 6. pp. 415-421, 2007.
, “HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics”, vol. 6, pp. 453-460, 2007.
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