ABSTRACT. We looked for abnormal hemoglobins in blood samples sent for diagnosis of anemia. Identification of the hemoglobins was made using electrophoretic, chromatographic and molecular procedures. The 2020 blood samples were of patients from various regions of Brazil and from some other Latin American countries. Among the abnormal hemoglobins that we found, 3.5 % are known to be rare, while 51% had an electrophoretic profile similar to that of Hb S at alkaline pH. Differentiation was possible only by combining electrophoretic and chromatographic methods. Hb Hasharon, an alpha globin chain mutant, was the most frequently found variant hemoglobin; it accounted for 14.3 % of the abnormal DNA samples. The other abnormal hemoglobin phenotypes...
Between 1978 and 2009, we studied 1,863 Mexican Mestizo patients with clinical data compatible with ...
Inherited disorders of hemoglobin, the most common monogenic disease, are now well understood at the...
We identified the -globin gene alterations present in 20 carriers of Hb Fetal structural variants an...
The human hemoglobins, with genetically defined inheritance patterns, have shown characteristic poly...
Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While screenings fo...
Foram analisadas 7.657 amostras de sangue provenientes de 48 cidades das regiões de São José do Rio ...
Background: Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While s...
Hemoglobin variants originate mainly by simple amino acid substitutions, the result of nucleotide se...
Introduction: Hemoglobinopathies are considered a major public health problem in many countries, inc...
9ª Reunião Científica da Sociedade Portuguesa de Medicina Laboratorial, 7-8 abril 2017Hemoglobinopat...
Introduction. Hemoglobin disorders are classified into three main groups: structural variants, thala...
Hemoglobin profile studies have been carried out in four samples from different districts of Porto V...
Hemoglobinopathies are the most common recessive diseases worldwide but their prevalence in Uruguay ...
Hemoglobin structural abnormalities are among the most commonly found human genetic diseases. The La...
Hemoglobin profile studies have been carried out in four samples from different districts of Porto V...
Between 1978 and 2009, we studied 1,863 Mexican Mestizo patients with clinical data compatible with ...
Inherited disorders of hemoglobin, the most common monogenic disease, are now well understood at the...
We identified the -globin gene alterations present in 20 carriers of Hb Fetal structural variants an...
The human hemoglobins, with genetically defined inheritance patterns, have shown characteristic poly...
Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While screenings fo...
Foram analisadas 7.657 amostras de sangue provenientes de 48 cidades das regiões de São José do Rio ...
Background: Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While s...
Hemoglobin variants originate mainly by simple amino acid substitutions, the result of nucleotide se...
Introduction: Hemoglobinopathies are considered a major public health problem in many countries, inc...
9ª Reunião Científica da Sociedade Portuguesa de Medicina Laboratorial, 7-8 abril 2017Hemoglobinopat...
Introduction. Hemoglobin disorders are classified into three main groups: structural variants, thala...
Hemoglobin profile studies have been carried out in four samples from different districts of Porto V...
Hemoglobinopathies are the most common recessive diseases worldwide but their prevalence in Uruguay ...
Hemoglobin structural abnormalities are among the most commonly found human genetic diseases. The La...
Hemoglobin profile studies have been carried out in four samples from different districts of Porto V...
Between 1978 and 2009, we studied 1,863 Mexican Mestizo patients with clinical data compatible with ...
Inherited disorders of hemoglobin, the most common monogenic disease, are now well understood at the...
We identified the -globin gene alterations present in 20 carriers of Hb Fetal structural variants an...