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Molecular identification of Sicilian (deltaß)º-thalassemia associated with ß-thalassemia and hemoglobin S in Brazil
(Associação Brasileira de Divulgação Científica, 2002)
Molecular identification of Sicilian (8 beta)degrees-thalassemia associated with beta-thalassemia and hemoglobin S in Brazil
(Assoc Bras Divulg CientificaSao PauloBrasil, 2002)
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 ...
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)
Alpha-thalassemia. Case report alpha-thalassemia in a Costa Rican family, A case report
(2020-11-26)
This case report highlights the importance for health care providers to be aware of the αlpha‐thalassemia syndromes, their relevance to clinical care and family counseling, appropriate diagnostic algorithm for definitive ...
Camperdown hemoglobin associated with beta degrees thalassemia in a Brazilian child
(Soc Brasil GeneticaRibeirao PretBrasil, 2005)
Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
(2011-12-01)
Fetal hemoglobin (Hb F) is characteristic of the fetal development period. However, in some genetic conditions, such as hereditary persistence of fetal hemoglobin (HPFH) and delta-beta thalassemia (δβ-thalassemia), Hb F ...
Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
(2011-12-01)
Fetal hemoglobin (Hb F) is characteristic of the fetal development period. However, in some genetic conditions, such as hereditary persistence of fetal hemoglobin (HPFH) and delta-beta thalassemia (δβ-thalassemia), Hb F ...