Current Standards of Care and Long Term Outcomes for Thalassemia and Sickle Cell Disease.
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DOI: 10.1007/978-1-4939-7299-9_3
Abstract: Thalassemia and sickle cell disease (SCD) are disorders of hemoglobin that affect millions of people worldwide. The carrier states for these diseases arose as common, balanced polymorphisms during human history because they afforded protection against… read more here.
Keywords: thalassemia sickle; cell disease; sickle cell; current standards ... See more keywords
Consequences of β-Thalassemia or Sickle Cell Disease for Ovarian Follicle Number and Morphology in Girls Who Had Ovarian Tissue Cryopreserved
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DOI: 10.3389/fendo.2020.593718
Abstract: Women with β-thalassemia (BT) and sickle cell disease (SCD) have a high risk of infertility and premature ovarian insufficiency. Different fertility preserving strategies, including ovarian tissue cryopreservation (OTC) and oocyte cryopreservation has been considered, and… read more here.
Keywords: ovarian tissue; follicle; cell disease; thalassemia sickle ... See more keywords
Redox Balance in β-Thalassemia and Sickle Cell Disease: A Love and Hate Relationship
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DOI: 10.3390/antiox11050967
Abstract: β-thalassemia and sickle cell disease (SCD) are inherited hemoglobinopathies that result in both quantitative and qualitative variations in the β-globin chain. These in turn lead to instability in the generated hemoglobin (Hb) or to a… read more here.
Keywords: cell; thalassemia sickle; thalassemia; redox balance ... See more keywords
Pharmacological Induction of Fetal Hemoglobin in β-Thalassemia and Sickle Cell Disease: An Updated Perspective
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DOI: 10.3390/ph15060753
Abstract: A significant amount of attention has recently been devoted to the mechanisms involved in hemoglobin (Hb) switching, as it has previously been established that the induction of fetal hemoglobin (HbF) production in significant amounts can… read more here.
Keywords: thalassemia sickle; cell disease; induction fetal; fetal hemoglobin ... See more keywords