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Molecular identification of Sicilian (8 beta)degrees-thalassemia associated with beta-thalassemia and hemoglobin S in Brazil
(Assoc Bras Divulg CientificaSao PauloBrasil, 2002)
Thalassemia intermedia as a result of heterozygosis for beta(0)-thalassemia and alpha alpha alpha(anti-3.7)/alpha alpha genotype in a Brazilian patient
(Assoc Bras Divulg CientificaSao PauloBrasil, 2003)
HFE gene mutations in Brazilian thalassemic patients
(2006-12-01)
Hereditary hemochromatosis is a disorder of iron metabolism characterized by increased iron intake and progressive storage and is related to mutations in the HFE gene. Interactions between thalassemia and hemochromatosis ...
HFE gene mutations in Brazilian thalassemic patients
(2006-12-01)
Hereditary hemochromatosis is a disorder of iron metabolism characterized by increased iron intake and progressive storage and is related to mutations in the HFE gene. Interactions between thalassemia and hemochromatosis ...
Camperdown hemoglobin associated with beta degrees thalassemia in a Brazilian child
(Soc Brasil GeneticaRibeirao PretBrasil, 2005)
Oxidative stress and antioxidant status in beta-thalassemia heterozygotes
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2013)
Background:Several studies have evaluated the oxidant and antioxidant status of thalassemia patients but most focused mainly on the severe and intermediate states of the disease. Moreover, the oxidative status has not been ...