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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 ...
Amputations In Sickle Cell Disease: Case Series And Literature Review
(TAYLOR & FRANCIS LTDABINGDON, 2016)
Sub capsular splenic hematoma in a sickle cell trait carrier. case report Hematoma subcapsular esplénico en paciente portador de rasgo falciforme
(2011)
Drepanocytic anemia is an uncommon hereditary disease in Chile. The heterozygous state of drepanocytic anemia or "sickle trait" has a frequency of 8% among Afro-Americans. A small number of patients carrying hemoglobin S ...
Proliferative sickle cell retinopathy associated with sickle cell trait and gestational diabetes: case report
(Conselho Brasileiro de Oftalmologia, 2009)
Proliferative sickle cell retinopathy is an uncommon complication in individuals with sickle cell trait (AS). However, the risk for proliferative retinopathy development is increased in patients with AS hemoglobinopathy ...
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 ...
Elastic properties of stored red blood cells from sickle trait donor units
(Blackwell Publishing LtdOxfordInglaterra, 2003)
Renal medullary carcinoma - Case report and review of the literature
(KargerBaselSuíça, 2006)