Factor X Friuli coagulation disorder. First report of a patient born in Friuli after the description of the disease.

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作者信息

Girolami A, Carli A, Falomo R, De Marco L

出版信息

Blut. 1973 Sep;27(3):151-8. doi: 10.1007/BF01634029.

DOI:10.1007/BF01634029

PMID:4762001

Abstract

摘要

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引用本文的文献

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.

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Factor X Friuli: An immunological study in plasma and in serum using several methods.

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本文引用的文献

THE INHERITANCE OF STUART DISEASE: INVESTIGATION OF A FAMILY WITH FACTOR X DEFICIENCY.

Am J Med Sci. 1965 Mar;249:291-4. doi: 10.1097/00000441-196503000-00006.

[Description of a technic simultaneously combining electrophoresis and immunological precipitation in gel: electrosyneresis].[一种在凝胶中同时结合电泳和免疫沉淀的技术描述：电凝缩]

Biochim Biophys Acta. 1959 Jul;34:258-60. doi: 10.1016/0006-3002(59)90261-6.

[A new congenital coagulation defect; Stuart factor defect].

Thromb Diath Haemorrh. 1958 Apr 15;1(1):87-92.

Stuart clotting defect. II. Genetic aspects of a new hemorrhagic state.斯图尔特凝血缺陷。二、一种新的出血状态的遗传学方面。

J Clin Invest. 1957 Mar;36(3):497-503. doi: 10.1172/JCI103447.

Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency.斯图尔特凝血缺陷。I. 从迄今为止称为稳定因子（血清凝血酶原转变加速素、前转变素、因子VII）缺乏的异质性组中分离出一种遗传性出血状态。

J Clin Invest. 1957 Mar;36(3):485-96. doi: 10.1172/JCI103446.

A new coagulation defect.一种新的凝血缺陷。

Br J Haematol. 1956 Jul;2(3):308-16. doi: 10.1111/j.1365-2141.1956.tb06703.x.

Severe congenital factor X deficiency in 5-month-old child.

Thromb Diath Haemorrh. 1970 Oct 31;24(1):175-84.

Congenital haemorrhagic condition similar but not identical to factor X deficiency. A haemorrhagic state due to an abnormal factor X?

Scand J Haematol. 1970;7(2):91-9. doi: 10.1111/j.1600-0609.1970.tb01874.x.

[A new congenital hemorrhagic coagulation disorder probably due to the presence of an abnormal factor X. Preliminary study].[一种可能由异常X因子导致的新型先天性出血性凝血障碍。初步研究]

Minerva Med. 1969 Dec 8;60(98):4939-49.

Prothrombin level and activity in the abnormal factor X (factor X Friuli) hemorrhagic disorder.

Thromb Diath Haemorrh. 1971;25(1):147-56.

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