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.
Abstract
摘要
相似文献
1
Sickle-cell disease: a call to action.镰状细胞病：行动呼吁。
Trans R Soc Trop Med Hyg. 2015 Jun;109(6):355-6. doi: 10.1093/trstmh/trv035.
2
Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years.镰状细胞病的演变：从危及儿童生命的疾病到成人慢性病：过去的 40 年。
Am J Hematol. 2016 Jan;91(1):5-14. doi: 10.1002/ajh.24235.
3
Management of sickle-cell disease.镰状细胞病的管理
J Clin Pathol Suppl (R Coll Pathol). 1974;8:26-31.
4
Pitfalls in newborn hemoglobinopathy screening: failure to detect beta(+)-thalassemia.
J Pediatr. 1995 Aug;127(2):304-8. doi: 10.1016/s0022-3476(95)70316-0.
5
OCCURRENCE OF UNUSUAL HAEMOGLOBINOPATHIES IN BALOCHISTAN: HB SD AND HB SE - PRESENTATION WITH OSTEOMYELITIS.俾路支省罕见血红蛋白病的发生：HB SD 和 HB SE - 伴有骨髓炎。
Rev Paul Pediatr. 2021 Feb 3;39:e2019365. doi: 10.1590/1984-0462/2021/39/2019365. eCollection 2021.
6
Prophylaxis crucial in sickle cell disease.
Practitioner. 2007 Jul;251(1696):55, 57, 59-61.
7
Preventive hematology.
Indian J Med Sci. 1993 Jul;47(7):185-90.
8
Neonatal Screening and the Clinical Outcome in Children with Sickle Cell Disease in Central India.印度中部镰状细胞病患儿的新生儿筛查及临床结局
PLoS One. 2016 Jan 19;11(1):e0147081. doi: 10.1371/journal.pone.0147081. eCollection 2016.
9
[Neonatal screening for sickle cell disease at the Nice University Hospital: the last 8 years].[尼斯大学医院新生儿镰状细胞病筛查：过去8年]
Arch Pediatr. 2010 Dec;17(12):1652-6. doi: 10.1016/j.arcped.2010.09.011. Epub 2010 Nov 17.
10
Sickle cell disease in North Europe.北欧的镰状细胞病。
Scand J Clin Lab Invest. 2007;67(1):27-38. doi: 10.1080/00365510601046441.
引用本文的文献
1
Newborn Screening for Sickle Cell Disease: Results from a Pilot Study in the Portuguese Population.镰状细胞病的新生儿筛查：葡萄牙人群试点研究结果
Int J Neonatal Screen. 2025 Jan 27;11(1):10. doi: 10.3390/ijns11010010.
2
Healthcare Professionals' Knowledge, Attitudes, and Practices in the Assessment, and Management of Sickle-Cell Disease: A Meta-Aggregative Review.医疗保健专业人员在镰状细胞病评估与管理中的知识、态度和实践：一项元聚合综述
Diseases. 2024 Jul 14;12(7):156. doi: 10.3390/diseases12070156.
3
Jk(a) (Kidd-A) Variant in a Sickle Cell Disease Patient.一名镰状细胞病患者中的Jk(a)（基德-A）变异型
Cureus. 2023 Nov 26;15(11):e49451. doi: 10.7759/cureus.49451. eCollection 2023 Nov.
4
Quantifying the Levels of Knowledge, Attitude, and Practice Associated with Sickle Cell Disease and Premarital Genetic Counseling in 350 Saudi Adults.量化350名沙特成年人中与镰状细胞病及婚前遗传咨询相关的知识、态度和行为水平。
Adv Hematol. 2019 May 2;2019:3961201. doi: 10.1155/2019/3961201. eCollection 2019.
5
Human hemoglobin G-Makassar variant masquerading as sickle cell anemia.伪装成镰状细胞贫血的人类血红蛋白G-望加锡变体。
Hematol Rep. 2018 Sep 24;10(3):7210. doi: 10.4081/hr.2018.7210. eCollection 2018 Sep 5.
6
Existence, triggers, and coping with chronic sorrow: a qualitative study of caretakers of children with sickle cell disease in a National Referral Hospital in Kampala, Uganda.慢性悲伤的存在、触发因素及应对：对乌干达坎帕拉一家国家转诊医院中镰状细胞病患儿照料者的定性研究
BMC Psychol. 2018 Oct 20;6(1):50. doi: 10.1186/s40359-018-0263-y.
7
Pulmonary function indices in children with sickle cell anemia in Enugu, south-east Nigeria.尼日利亚东南部埃努古镰状细胞贫血患儿的肺功能指标
Saudi Med J. 2015 Aug;36(8):928-34. doi: 10.15537/smj.2015.8.11525.
本文引用的文献
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.
Zotero 插件