Is sickle cell disease the same everywhere?
作者信息
Hankins Jane
机构信息
St. Jude Children's Research Hospital Memphis, TN, USA.
出版信息
Rev Bras Hematol Hemoter. 2012;34(3):178-9. doi: 10.5581/1516-8484.20120042.
Abstract
摘要
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本文引用的文献
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Sickle cell disease: acute clinical manifestations in early childhood and molecular characteristics in a group of children in Rio de Janeiro.镰状细胞病：里约热内卢一组儿童的幼儿期急性临床表现及分子特征
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Limitations of Hb F as a phenotypic modifier in sickle cell disease: study of Kuwaiti Arab patients.胎儿血红蛋白（Hb F）作为镰状细胞病表型修饰因子的局限性：科威特阿拉伯患者的研究
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Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India.印度东部β(S)和(G)γ((A)γδβ)⁰地中海贫血的临床与分子特征
Hemoglobin. 2010;34(6):604-9. doi: 10.3109/03630269.2010.526890.
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Coinheritance of α-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia.α地中海贫血的共同遗传降低了一组镰状细胞贫血儿童患脑血管疾病的风险。
Hemoglobin. 2010;34(6):516-29. doi: 10.3109/03630269.2010.526003.
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