Co-Inheritance of alpha-thalassemia and sickle cell disease in a cohort of Angolan pediatric patients
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DOI: 10.1007/s11033-020-05628-8
Abstract: The aim of this study was to explore the association between alpha-thalassemia, fetal hemoglobin, hematological indices, and clinical adverse events in Angolan sickle cell disease pediatric patients. A total of 200 sickle cell disease (SCD)… read more here.
Keywords: sickle cell; cell disease; alpha thalassemia; thalassemia ... See more keywords
Expression and prognostic impact of alpha thalassemia/mental retardation X-linked and death domain-associated protein in human lung cancer
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DOI: 10.1097/md.0000000000016712
Abstract: Supplemental Digital Content is available in the text read more here.
Keywords: alpha thalassemia; impact alpha; prognostic impact; mental retardation ... See more keywords
Screening of Some Indicators for Alpha-Thalassemia in Fujian Province of Southern China
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DOI: 10.2147/ijgm.s338419
Abstract: Background Carrier screening is the most effective means of controlling the prevalence of alpha-thalassemia. However, due to the differences in ethnic populations and genotypes, the distribution of mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH)… read more here.
Keywords: fujian province; china; thalassemia fujian; alpha thalassemia ... See more keywords
HbF-promoting polymorphisms may specifically reduce the residual risk of cerebral vasculopathy in SCA children with alpha-thalassemia.
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DOI: 10.3233/ch-200951
Abstract: Sickle cell anemia (SCA) is a disease characterized by abnormal red blood cell rheology. Because of their effects on HbS polymerization and red blood cell deformability, alpha-thalassemia and the residual HbF level are known genetic… read more here.
Keywords: hbf; cerebral vasculopathy; sca; thalassemia ... See more keywords