Homozygous Prekallikrein Deficiency in the USA: Several Patients but Still Few Mutation Studies.
作者信息
Girolami Antonio, Ferrari Silvia
机构信息
Department of Medicine, University of Padua Medical School, Padua, Italy.
出版信息
Clin Appl Thromb Hemost. 2021 Jan-Dec;27:1076029621998773. doi: 10.1177/1076029621998773.
Abstract
摘要
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本文引用的文献
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J Thromb Haemost. 2021 Jan;19(1):147-152. doi: 10.1111/jth.15137. Epub 2020 Nov 18.
2
Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States.与美国普通人群相比，非裔美国人中报告的先天性前激肽释放酶缺乏症病例患病率增加。
Clin Appl Thromb Hemost. 2020 Jan-Dec;26:1076029620918301. doi: 10.1177/1076029620918301.
3
Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence.严重血浆前激肽释放酶缺乏症：临床特征、新型KLKB1突变及估计患病率
J Thromb Haemost. 2020 Jul;18(7):1598-1617. doi: 10.1111/jth.14805. Epub 2020 May 15.
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Lisinopril-Induced Angioedema in a Patient with Plasma Prekallikrein Deficiency.一名血浆前激肽释放酶缺乏患者发生赖诺普利诱导的血管性水肿。
TH Open. 2020 Jan 23;4(1):e33-e35. doi: 10.1055/s-0040-1701238. eCollection 2020 Jan.
5
Cardiovascular diseases in congenital prekallikrein deficiency: comparison with other chance-associated morbidities.先天性前激肽释放酶缺乏症中的心血管疾病：与其他偶发性相关疾病的比较。
Blood Coagul Fibrinolysis. 2018 Jul;29(5):423-428. doi: 10.1097/MBC.0000000000000735.
6
A structure-function analysis in patients with prekallikrein deficiency.前激肽释放酶缺乏症患者的结构-功能分析。
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A case of prekallikrein deficiency resulting in severe recurrent mucosal hemorrhage.一例因前激肽释放酶缺乏导致严重复发性黏膜出血的病例。
Am J Med Sci. 2009 Nov;338(5):429-30. doi: 10.1097/MAJ.0b013e3181b270bb.
8
Thrombosis or myocardial infarction in congenital clotting factor abnormalities and chronic thrombocytopenias: a report of 21 patients and a review of 50 previously reported cases.先天性凝血因子异常和慢性血小板减少症中的血栓形成或心肌梗死：21例报告及对50例既往报道病例的综述
Medicine (Baltimore). 1983 Jul;62(4):248-55. doi: 10.1097/00005792-198307000-00004.
9
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Ann Clin Lab Sci. 1985 Jul-Aug;15(4):279-85.
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