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Desnaturação de oxihemoglobinas humanas A, A2 e S pelo metodo de tampão isopropanol
(1978-12-01)
Human oxyhaemoglobin A and A2 from normal individuals and oxyhaemoglobin S from patients with sickle cell anaemia and sickle cell trait were studied using Isopropanol/buffer method at 37°C and 40°C. Hb S was less stable ...
HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics
(2007-09-03)
The purpose of the present study was to establish reference values for hemoglobins (Hb) using HPLC, in samples containing normal Hb (AA), sickle cell trait without alpha-thalassemia (AS), sickle cell trait with alpha-thalassemia ...
HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics
(2007-09-03)
The purpose of the present study was to establish reference values for hemoglobins (Hb) using HPLC, in samples containing normal Hb (AA), sickle cell trait without alpha-thalassemia (AS), sickle cell trait with alpha-thalassemia ...
Desnaturação de oxihemoglobinas humanas A, A2 e S pelo metodo de tampão isopropanol
(1978-12-01)
Human oxyhaemoglobin A and A2 from normal individuals and oxyhaemoglobin S from patients with sickle cell anaemia and sickle cell trait were studied using Isopropanol/buffer method at 37°C and 40°C. Hb S was less stable ...
Hemoglobin Polymorphism and Morphometrical Correlates in the West African Dwarf Sheep of Nigeria
(Sociedad Chilena de Anatomía, 2010)
alpha-thalassemia does not significantly contribute to the low MCV level of Hb C trait
(Marcel Dekker IncNew YorkEUA, 2002)
Hemoglobin as AS/alfa talassemia - Importância diagnóstica
(2000-12-01)
Sickle Cell disease is a generic term for a group of genetic disorders characterized by the predominance of hemoglobin S. These disorders include Sickle Cell anemia, the Sickle Cell beta Thalassemia syndromes and ...