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The vaso-occlusive crisis of sickle cell disease.

作者信息

Davies S C

出版信息

BMJ. 1991 Jun 29;302(6792):1551-2. doi: 10.1136/bmj.302.6792.1551.

DOI:10.1136/bmj.302.6792.1551
PMID:1855038
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1670351/
Abstract
摘要

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The vaso-occlusive crisis of sickle cell disease.镰状细胞病的血管阻塞性危机
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Addressing challenges of clinical trials in acute pain: The Pain Management of Vaso-occlusive Crisis in Children and Young Adults with Sickle Cell Disease Study.应对急性疼痛临床试验的挑战：镰状细胞病儿童和青年血管闭塞性危机的疼痛管理研究。
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Acute management of sickle cell crisis in pregnancy.孕期镰状细胞危象的急性处理
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引用本文的文献

1
Orbital Infarction due to Sickle Cell Disease without Orbital Pain.镰状细胞病所致眼眶梗死且无眼眶疼痛
Case Rep Ophthalmol Med. 2016;2016:5867850. doi: 10.1155/2016/5867850. Epub 2016 Nov 7.
2
Sickle cell disease: the case for coordinated information.镰状细胞病：信息协调的情况
BMJ. 1993 Jun 5;306(6891):1491-2. doi: 10.1136/bmj.306.6891.1491.
3
Practical management of pain in sickling disorders.镰状细胞病疼痛的实际管理
Arch Dis Child. 1993 Aug;69(2):256-9. doi: 10.1136/adc.69.2.256.
4
Minimally invasive surgery in sickle cell disease.镰状细胞病的微创手术
BMJ. 1991 Jul 27;303(6796):249. doi: 10.1136/bmj.303.6796.249.
5
Pethidine for painful crises in sickle cell disease.哌替啶用于镰状细胞病的疼痛危象
BMJ. 1991 Jul 27;303(6796):249. doi: 10.1136/bmj.303.6796.249-a.

本文引用的文献

1
Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin.人类血红蛋白中的基因突变：正常血红蛋白与镰状细胞血红蛋白的化学差异。
Nature. 1957 Aug 17;180(4581):326-8. doi: 10.1038/180326a0.
2
Acute admissions of patients with sickle cell disease who live in Britain.居住在英国的镰状细胞病患者的急性入院情况。
Br Med J (Clin Res Ed). 1987 May 9;294(6581):1206-8. doi: 10.1136/bmj.294.6581.1206.
3
Red cell alloimmunization in sickle cell disease.镰状细胞病中的红细胞同种免疫
Br J Haematol. 1986 Jun;63(2):241-5. doi: 10.1111/j.1365-2141.1986.tb05546.x.
4
Bone marrow transplantation in five children with sickle cell anaemia.五名镰状细胞贫血患儿的骨髓移植
Lancet. 1988 Jun 25;1(8600):1427-8. doi: 10.1016/s0140-6736(88)92239-8.
5
The presentation, management and prophylaxis of sickle cell disease.镰状细胞病的临床表现、治疗与预防
Blood Rev. 1989 Mar;3(1):29-44. doi: 10.1016/0268-960x(89)90023-4.
6
Sickle erythrocytes inhibit human endothelial cell DNA synthesis.镰状红细胞抑制人内皮细胞DNA合成。
Blood. 1990 Nov 15;76(10):2146-52.
7
Beyond hemoglobin polymerization: the red blood cell membrane and sickle disease pathophysiology.
Blood. 1991 Jan 15;77(2):214-37.
8
Current concerns in haematology. 1. Is the painful crisis of sickle cell disease a "steal" syndrome?血液学当前关注的问题。1. 镰状细胞病的疼痛危象是一种“盗血”综合征吗？
J Clin Pathol. 1990 Oct;43(10):789-91. doi: 10.1136/jcp.43.10.789.
9
Treatment of sickle cell anemia with hydroxyurea and erythropoietin.用羟基脲和促红细胞生成素治疗镰状细胞贫血。
N Engl J Med. 1990 Aug 9;323(6):366-72. doi: 10.1056/NEJM199008093230602.