Buscar
Mostrando ítems 1-10 de 119
Molecular identification of Sicilian (deltaß)º-thalassemia associated with ß-thalassemia and hemoglobin S in Brazil
(Associação Brasileira de Divulgação Científica, 2002)
Thalassemia intermedia as a result of heterozygosis for ß0-thalassemia and aaaanti-3.7/aa genotype in a Brazilian patient
(Associação Brasileira de Divulgação Científica, 2003)
Urinary iron excretion induced by intravenous infusion of deferoxamine in ß-thalassemia homozygous patients
(Associação Brasileira de Divulgação Científica, 2002-11-01)
The purpose of the present study was to identify noninvasive methods to evaluate the severity of iron overload in transfusion-dependent ß-thalassemia and the efficiency of intensive intravenous therapy as an additional ...
Interaction between Hb SS and alpha thalassemia (3.7 kb deletion): a familial study
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2011-06-01)
Regression of extramedullary hematopoiesis with hydroxyurea therapy in ß-thalassemia intermedia
(Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular, 2006-03-01)
Excessive ineffective erythropoiesis in thalassemia intermedia may cause extramedullary hematopoiesis (EMH), resulting in spleen and liver enlargement or masses in several tissues, mainly paravertebrally. Other less frequent ...
Serum haptoglobin types in patients with hemoglobinopathies
(1990-12-01)
Haptoglobin types were determined in 626 individuals living in the State of Sao Paulo (Brazil). Of these, 484 had Hb AA, 31 major beta thalassemia, 43 minor beta thalassemia, 14 Hb SS, and 54 Hb AS. Frequency distribution ...
Serum haptoglobin types in patients with hemoglobinopathies
(1990-12-01)
Haptoglobin types were determined in 626 individuals living in the State of Sao Paulo (Brazil). Of these, 484 had Hb AA, 31 major beta thalassemia, 43 minor beta thalassemia, 14 Hb SS, and 54 Hb AS. Frequency distribution ...
Prevalence of beta(S)-globin gene haplotypes, alpha-thalassemia (3.7 kb deletion) and redox status in patients with sickle cell anemia in the state of Parana, Brazil
(Soc Brasil Genetica, 2015-01-01)
The aim of this study was to determine the frequency of beta S-globin gene (beta(S) globin) haplotypes and alpha thalassemia with 3.7 kb deletion (-alpha(3.7kb) thalassemia) in the northwest region of Parana state, and to ...
Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia
(Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular, 2014-10-01)
Objectives: To analyze the frequency of βS-globin haplotypes and alpha-thalassemia, and their influence on clinical manifestations and the hematological profile of children with sickle cell anemia.Method: The frequency of ...