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Abnormal factor X (factor X Friuli) coagulation disorder. The heterozygote population. A study of 57 subjects.

作者信息

Girolami A, Brunetti A, Bareggi G, Cella G

出版信息

Acta Haematol. 1974;51(1):40-50. doi: 10.1159/000208273.

DOI:10.1159/000208273
PMID:4217072
Abstract
摘要

相似文献

1
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.
2
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。
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3
A family with heterozygous factor X Friuli defect outside Friuli.
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Prothrombin level and activity in the abnormal factor X (factor X Friuli) hemorrhagic disorder.
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Further studies on the abnormal factor X (factor X Friuli) coagulation disorder. A report of another family.
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A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): study of a large kindred.
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Further studies on the abnormal factor X (factor X Friuli) coagulation disorder: a report of another family.
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8
Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern.帕多瓦因子VII：一种由于具有特殊激活模式的异常因子VII导致的先天性凝血障碍。
J Lab Clin Med. 1978 Mar;91(3):387-95.
9
Factor X Friuli coagulation disorder. First report of a patient born in Friuli after the description of the disease.
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10
The effect of several tissue thromboplastins on the activation of the abnormal factor X (factor X Friuli).几种组织凝血活酶对异常X因子（弗留利X因子）激活的影响。
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引用本文的文献

1
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.
2
Demonstration of a double hereditary pattern for congenital afibrinogenemia.先天性无纤维蛋白原血症的双遗传模式证明。
Blut. 1981 Oct;43(4):249-56. doi: 10.1007/BF00320454.
3
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.
4
A family with heterozygous factor X Friuli defect outside Friuli.
Blut. 1983 Mar;46(3):149-54. doi: 10.1007/BF00320273.
5
Factor X Friuli: An immunological study in plasma and in serum using several methods.
Blut. 1975 Mar;30(3):203-12. doi: 10.1007/BF01633955.
6
Combined functional and immunochemical analysis of normal and abnormal human factor X.正常与异常人凝血因子X的联合功能及免疫化学分析
J Clin Invest. 1979 Oct;64(4):884-94. doi: 10.1172/JCI109554.