A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): study of a large kindred.
作者信息
Girolami A, Molaro G, Lazzarin M, Scarpa R, Brunetti A
出版信息
Br J Haematol. 1970 Aug;19(2):179-92. doi: 10.1111/j.1365-2141.1970.tb01615.x.
Abstract
摘要
相似文献
1
A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): study of a large kindred.
Br J Haematol. 1970 Aug;19(2):179-92. doi: 10.1111/j.1365-2141.1970.tb01615.x.
2
Further studies on the abnormal factor X (factor X Friuli) coagulation disorder: a report of another family.
Blood. 1971 May;37(5):534-41.
3
[Congenital coagulopathy due to the presence of an abnormal factor X (Friuli factor X). A "new" hemorrhagic disease].[因异常X因子（弗留利X因子）存在导致的先天性凝血病。一种“新”的出血性疾病]
Recenti Prog Med. 1970 Oct;49(4):360-84.
4
Prothrombin level and activity in the abnormal factor X (factor X Friuli) hemorrhagic disorder.
Thromb Diath Haemorrh. 1971;25(1):147-56.
5
Laboratory diagnosis of congenital coagulation defects.先天性凝血缺陷的实验室诊断。
Clin Haematol. 1979 Feb;8(1):79-94.
6
Abnormal factor X (factor X Friuli) coagulation disorder. The heterozygote population. A study of 57 subjects.
Acta Haematol. 1974;51(1):40-50. doi: 10.1159/000208273.
7
Factor X Friuli coagulation disorder. Report of a newly recognized patient and some considerations on the frequency of the disease in the Friuli area.弗留利X因子凝血障碍。一例新确诊患者的报告及对弗留利地区该病发病率的一些思考。
Acta Haematol. 1976;56(1):27-38. doi: 10.1159/000207916.
8
A family with heterozygous factor X Friuli defect outside Friuli.
Blut. 1983 Mar;46(3):149-54. doi: 10.1007/BF00320273.
9
An approach to the diagnosis of disorders of hemostasis.一种止血障碍的诊断方法。
Mod Treat. 1968 Jan;5(1):11-38.
10
Another patient with a congenital hemorrhagic disorder intermediate between factor X and factor VII deficiency.另一名患有先天性出血性疾病的患者，其病情介于因子X缺乏和因子VII缺乏之间。
Haematol Lat. 1970 Jan-Mar;13(1):89-102.
引用本文的文献
1
Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period.在长期观察期间，严重 FXII 缺乏症患者与未受影响的家族成员相比发生血栓事件的情况。
J Thromb Thrombolysis. 2019 Apr;47(3):481-485. doi: 10.1007/s11239-019-01819-8.
2
New clotting disorders that cast new light on blood coagulation and may play a role in clinical practice.新的凝血障碍为血液凝固带来了新的认识，并可能在临床实践中发挥作用。
J Thromb Thrombolysis. 2017 Jul;44(1):71-75. doi: 10.1007/s11239-017-1488-y.
3
Factor X Friuli Coagulation Disorder: Almost 50 Years Later.弗留利X因子凝血障碍：近50年后
Clin Appl Thromb Hemost. 2018 Jan;24(1):33-40. doi: 10.1177/1076029616686423. Epub 2016 Dec 29.
4
Pregnancies and oral contraceptive therapy in severe (homozygons) FXII deficiency: a study in 12 patients and review of the literature.严重（纯合子）因子Ⅻ缺乏症患者的妊娠及口服避孕药治疗：12例患者的研究及文献综述
J Thromb Thrombolysis. 2004 Dec;18(3):209-12. doi: 10.1007/s11239-005-0348-3.
5
The occasional venous thromboses seen in patients with severe (homozygous) FXII deficiency are probably due to associated risk factors: a study of prevalence in 21 patients and review of the literature.对21例严重（纯合子）FXII缺乏症患者中偶尔出现的静脉血栓形成的研究及文献回顾表明，这些血栓形成可能归因于相关危险因素。
J Thromb Thrombolysis. 2004 Apr;17(2):139-43. doi: 10.1023/B:THRO.0000037670.42776.cd.
6
Symptomatic combined homozygous factor XII deficiency and heterozygous factor V Leiden. luscaber@tin.it.有症状的纯合子因子 XII 缺乏症合并杂合子因子 V 莱顿突变。luscaber@tin.it。
J Thromb Thrombolysis. 2000 Apr;9(3):271-5. doi: 10.1023/a:1018774813568.
7
Different organization of von Willebrand factor oligomers in type-2A and -2B von Willebrand disease variants: effects of DDAVP infusion and protease inhibitors.2A型和2B型血管性血友病变异体中血管性血友病因子寡聚体的不同组织形式：去氨加压素输注和蛋白酶抑制剂的作用
Ann Hematol. 1995 Oct;71(4):189-94. doi: 10.1007/BF01910317.
8
Further studies on factor VII Padua defect: the report of the fourth homozygous patient from the same valley.
Blut. 1982 Jun;44(6):363-9. doi: 10.1007/BF00319920.
9
Inherited coagulation disorders in India.印度的遗传性凝血障碍
Indian J Pediatr. 1981 Jul-Aug;48(393):525-31. doi: 10.1007/BF02822303.
10
A new family with classical factor X deficiency as demonstrated by electroimmunoassay.通过免疫电泳法证实的一个患有典型因子X缺乏症的新家族。
Blut. 1983 Jul;47(1):53-7. doi: 10.1007/BF00321050.
Zotero 插件