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Sickle cell anemia: clinical diversity and beta S-globin haplotypes.

作者信息

Loggetto Sandra Regina

机构信息

Centro de Hematologia de São Paulo - CHSP, São Paulo, SP, Brazil.

出版信息

Rev Bras Hematol Hemoter. 2013;35(3):155-7. doi: 10.5581/1516-8484.20130048.

Abstract
摘要

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本文引用的文献

1
Kidney dysfunction and beta S-haplotypes in patients with sickle cell disease.
Rev Bras Hematol Hemoter. 2013;35(3):171-3. doi: 10.5581/1516-8484.20130052.
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Impact of β(S)-globin haplotypes on oxidative stress in patients with sickle cell anemia in steady state.
Arch Med Res. 2012 Oct;43(7):536-40. doi: 10.1016/j.arcmed.2012.08.014. Epub 2012 Oct 19.
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Determination of β haplotypes in patients with sickle-cell anemia in the state of Rio Grande do Norte, Brazil.
Genet Mol Biol. 2011 Jul;34(3):421-4. doi: 10.1590/S1415-47572011005000027. Epub 2011 Jul 1.
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Genetic polymorphisms and cerebrovascular disease in children with sickle cell anemia from Rio de Janeiro, Brazil.
Arq Neuropsiquiatr. 2011 Jun;69(3):431-5. doi: 10.1590/s0004-282x2011000400004.
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β-globin haplotypes in normal and hemoglobinopathic individuals from Reconcavo Baiano, State of Bahia, Brazil.
Genet Mol Biol. 2010 Jul;33(3):411-7. doi: 10.1590/S1415-47572010005000042. Epub 2010 Sep 1.
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Alpha-thalassemia is associated with a decreased occurrence and a delayed age-at-onset of albuminuria in sickle cell anemia patients.
Blood Cells Mol Dis. 2010 Aug 15;45(2):154-8. doi: 10.1016/j.bcmd.2010.06.003. Epub 2010 Jul 3.

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