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1
Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?喀麦隆人中的β-珠蛋白基因单倍型及全球分布综述：非洲镰状细胞突变是否起源于单一源头？
OMICS. 2015 Mar;19(3):171-9. doi: 10.1089/omi.2014.0134.
2
Variable phenotypes of sickle cell disease in India with the Arab-Indian haplotype.印度镰状细胞病的可变表型与阿拉伯-印度单倍型。
Br J Haematol. 2015 Jan;168(1):156-9. doi: 10.1111/bjh.13083. Epub 2014 Aug 19.
3
Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.沙特阿拉伯的镰状细胞病：具有阿拉伯-印度单倍型的成年人的表型并非良性。
Br J Haematol. 2014 Feb;164(4):597-604. doi: 10.1111/bjh.12650. Epub 2013 Nov 13.
4
Evidence review of hydroxyurea for the prevention of sickle cell complications in low-income countries.羟脲预防低收入国家镰状细胞并发症的证据回顾。
Arch Dis Child. 2013 Nov;98(11):908-14. doi: 10.1136/archdischild-2012-302387. Epub 2013 Aug 30.
5
Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions.2010-2050 年期间五岁以下儿童镰状细胞性贫血的全球负担：基于人口统计学、超额死亡率和干预措施的建模研究。
PLoS Med. 2013;10(7):e1001484. doi: 10.1371/journal.pmed.1001484. Epub 2013 Jul 16.
6
Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimates.全球新生儿镰状细胞血红蛋白病流行病学：基于当代地统计学模型的地图和人群估计。
Lancet. 2013 Jan 12;381(9861):142-51. doi: 10.1016/S0140-6736(12)61229-X. Epub 2012 Oct 25.
7
World distribution, population genetics, and health burden of the hemoglobinopathies.血红蛋白病的世界分布、人口遗传学和健康负担。
Cold Spring Harb Perspect Med. 2012 Sep 1;2(9):a011692. doi: 10.1101/cshperspect.a011692.
8
Sickle-cell disease.镰状细胞病。
Lancet. 2010 Dec 11;376(9757):2018-31. doi: 10.1016/S0140-6736(10)61029-X. Epub 2010 Dec 3.
9
The inherited diseases of hemoglobin are an emerging global health burden.血红蛋白遗传疾病是一个正在浮现的全球性健康负担。
Blood. 2010 Jun 3;115(22):4331-6. doi: 10.1182/blood-2010-01-251348. Epub 2010 Mar 16.
10
Bacteraemia in Kenyan children with sickle-cell anaemia: a retrospective cohort and case-control study.肯尼亚镰状细胞贫血患儿的菌血症：一项回顾性队列研究和病例对照研究。
Lancet. 2009 Oct 17;374(9698):1364-70. doi: 10.1016/S0140-6736(09)61374-X. Epub 2009 Sep 9.

Sickle-cell disease: a call to action.

作者信息

Piel Frédéric B, Weatherall David J

机构信息

Department of Zoology, University of Oxford, Oxford, OX1 3PS, UK

MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, OX3 9DS, UK.

出版信息

Trans R Soc Trop Med Hyg. 2015 Jun;109(6):355-6. doi: 10.1093/trstmh/trv035.

DOI:10.1093/trstmh/trv035
PMID:25995293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4499945/
Abstract
摘要