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Severe factor V deficiency with prolonged bleeding time.

作者信息

Breederveld K, van Royen E A, Ten Cate J W

出版信息

Thromb Diath Haemorrh. 1974 Dec 31;32(2-3):538-48.

PMID:4450205
Abstract
摘要

相似文献

1
Severe factor V deficiency with prolonged bleeding time.严重的凝血因子V缺乏症伴出血时间延长。
Thromb Diath Haemorrh. 1974 Dec 31;32(2-3):538-48.
2
[Congenital factor V deficiency with thrombocytopathy].
Wien Z Inn Med. 1970;51(11):510-20.
3
[The concomitant presence of prohemorrhagic and thrombophilic changes in coagulation factor V: a severe defect of coagulant activity and homozygote resistance to activated protein C].
Ann Ital Med Int. 1999 Apr-Jun;14(2):127-9.
4
Congenital combined deficiency of factor V and factor 8. A case report and the effect of transfusion of normal plasma and hemophilic blood.先天性因子V和因子VIII联合缺乏症。一例病例报告及输注正常血浆和血友病血液的效果。
Thromb Diath Haemorrh. 1969 Nov 15;22(2):316-25.
5
Acquired haemophilia A associated with transitory and severe factor V deficiency during bullous pemphigoid: first report.
Thromb Haemost. 2009 Mar;101(3):582-3.
6
[Hemorrhagic disease caused by factor V deficiency (parahemophilia)].[因子V缺乏所致出血性疾病（副血友病）]
Recenti Prog Med. 1971 Jul;51(1):71-98.
7
Haemorrhagic symptoms in patients with combined factors V and VIII deficiency in north-eastern Iran.伊朗东北部同时存在因子V和因子VIII缺乏的患者的出血症状
Haemophilia. 2004 May;10(3):271-5. doi: 10.1111/j.1365-2516.2004.00890.x.
8
[Hereditary factor V deficiency and factor V inhibitor without bleeding. Rare causes of pathological screening tests of coagulation].[遗传性因子V缺乏症与无出血的因子V抑制剂。凝血病理筛查试验的罕见原因]
Hamostaseologie. 2007 Aug;27(3):188-90.
9
[Congenital factor V deficiency and intraventricular hemorrhage of prenatal origin].[先天性因子V缺乏与产前起源的脑室内出血]
Pediatr Med Chir. 1994 Jan-Feb;16(1):93-4.
10
Hemorrhagic varicella in parahemophilia.
Blut. 1972 Nov;25(5):293-301. doi: 10.1007/BF01631811.

引用本文的文献

1
Surgical correction of coarctation of the aorta and ventricular septal defect in an infant with inherited factor V deficiency.一名患有遗传性因子V缺乏症的婴儿的主动脉缩窄和室间隔缺损的外科矫正。
Pediatr Cardiol. 1983 Apr-Jun;4(2):169-70. doi: 10.1007/BF02076347.