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Familial multiple coagulation factor deficiencies. I. Review of the literature: Differentiation of single hereditary disorders associated with multiple factor deficiencies from coincidental concurrence of single factor deficiency states.

作者信息

Soff G A, Levin J

出版信息

Semin Thromb Hemost. 1981 Fall;7(2):112-48. doi: 10.1055/s-2007-1005073.

DOI:10.1055/s-2007-1005073
PMID:6794149
Abstract
摘要

相似文献

1
Familial multiple coagulation factor deficiencies. I. Review of the literature: Differentiation of single hereditary disorders associated with multiple factor deficiencies from coincidental concurrence of single factor deficiency states.家族性多种凝血因子缺乏症。I. 文献综述：与多种因子缺乏相关的单一遗传性疾病与单一因子缺乏状态偶然并发的鉴别。
Semin Thromb Hemost. 1981 Fall;7(2):112-48. doi: 10.1055/s-2007-1005073.
2
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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。
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引用本文的文献

1
Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis.大量患者队列中的家族性多种凝血因子缺乏症（FMCFDs）——单中心基因诊断经验
J Clin Med. 2021 Jan 18;10(2):347. doi: 10.3390/jcm10020347.
2
Hereditary combined deficiency of the vitamin K-dependent clotting factors.遗传性维生素 K 依赖性凝血因子缺乏症。
Orphanet J Rare Dis. 2010 Jul 14;5:21. doi: 10.1186/1750-1172-5-21.
3
Clinical manifestations of combined factor V and VIII deficiency: a series of 37 cases from a single center in India.
联合因子V和VIII缺乏症的临床表现：来自印度单一中心的37例病例系列
Am J Hematol. 2010 Jul;85(7):538-9. doi: 10.1002/ajh.21741.
4
Evidence of normal functional levels of activated protein C inhibitor in combined Factor V/VIII deficiency disease.联合因子V/ VIII缺乏症中活化蛋白C抑制剂功能水平正常的证据。
J Clin Invest. 1982 Dec;70(6):1260-72. doi: 10.1172/jci110725.
5
Association of congenital deficiency of multiple vitamin K-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivatives.多种维生素K依赖凝血因子先天性缺乏与华法林胚胎病表型的关联：香豆素衍生物致畸机制的线索
Am J Hum Genet. 1987 Oct;41(4):566-83.