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Prevalence and predictors of anemia in hereditary hemorrhagic telangiectasia.

作者信息

Kasthuri Raj S, Montifar Megan, Nelson Jeffrey, Kim Helen, Lawton Michael T, Faughnan Marie E

机构信息

Division of Hematology and Oncology, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Division of Respirology, Department of Medicine, St. Michael's Hospital, University of Toronto, Toronto, Canada.

出版信息

Am J Hematol. 2017 Jun 22. doi: 10.1002/ajh.24832.

DOI:10.1002/ajh.24832
PMID:28639385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5997494/
Abstract
摘要

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本文引用的文献

1
A systematic analysis of global anemia burden from 1990 to 2010.1990 年至 2010 年全球贫血负担的系统分析。
Blood. 2014 Jan 30;123(5):615-24. doi: 10.1182/blood-2013-06-508325. Epub 2013 Dec 2.
2
International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia.国际遗传性出血性毛细血管扩张症诊断和管理指南。
J Med Genet. 2011 Feb;48(2):73-87. doi: 10.1136/jmg.2009.069013. Epub 2009 Jun 23.
3
Prevalence of iron deficiency and health-related quality of life among female students.女学生中铁缺乏症的患病率及与健康相关的生活质量
J Am Coll Nutr. 2008 Apr;27(2):337-41. doi: 10.1080/07315724.2008.10719709.
4
Iron deficiency, general health and fatigue: results from the Australian Longitudinal Study on Women's Health.缺铁、总体健康状况与疲劳:澳大利亚女性健康纵向研究结果
Qual Life Res. 2000;9(5):491-7. doi: 10.1023/a:1008978114650.
5
Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).遗传性出血性毛细血管扩张症(伦杜-奥斯勒-韦伯综合征)的诊断标准。
Am J Med Genet. 2000 Mar 6;91(1):66-7. doi: 10.1002/(sici)1096-8628(20000306)91:1<66::aid-ajmg12>3.0.co;2-p.
6
Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients.遗传性出血性毛细血管扩张症:一项基于丹麦患者人群的患病率和死亡率研究。
J Intern Med. 1999 Jan;245(1):31-9. doi: 10.1046/j.1365-2796.1999.00398.x.