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An improved electrophoretic method for a screening program for haemoglobinopathies
(1980-12-01)
A method for a screening program for haemoglobinopathies in a starch agar gel mixed with saponin is presented. Normal and abnormal blood containing haemoglobins S, C, I, M Boston, D Punjab, beta thalassaemia major and beta ...
Abnormal hemoglobin phenotypes in carriers of mild anemia in Latin America.
(2010-05-26)
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 ...
Abnormal hemoglobin phenotypes in carriers of mild anemia in Latin America.
(2010-05-26)
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 ...
An improved electrophoretic method for a screening program for haemoglobinopathies
(1980-12-01)
A method for a screening program for haemoglobinopathies in a starch agar gel mixed with saponin is presented. Normal and abnormal blood containing haemoglobins S, C, I, M Boston, D Punjab, beta thalassaemia major and beta ...
Hemoglobin Kansas found by electrophoretic diagnosis in Brazil
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2002-03-01)
Hemoglobinas variantes com afinidade anormal ao oxigênio têm sido encontradas em várias partes do mundo. Pela sua afinidade ao oxigênio, estas hemoglobinas variantes têm sido classificadas e 15 variantes com baixa afinidade ...
Hemoglobin Kansas found by electrophoretic diagnosis in Brazil
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2014)
Severe Hemolytic Anemia due to De novo Hemoglobin Sabine in an argentinian newborn: first case in South America
(SCIENCEDOMAIN international, 2015)
Hemoglobin (Hb) Sabine is an unstable Hb variant that causes hemolytic anemia in heterozygous state, with inclusion bodies in the red blood cells (RBC). This hemoglobin is the result of a point mutation at codon 91(CTG)(CCG) ...