先天性因子 XIII 缺乏症中的 I 型和 II 型疾病。分类正确性的进一步证明。 - Suppr

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Type I and type II disease in congenital factor XIII deficiency. A further demonstration of the correctness of the classification.

作者信息

Girolami A, Cappellato M G, Lazzaro A R, Boscaro M

出版信息

Blut. 1986 Nov;53(5):411-3. doi: 10.1007/BF00321104.

DOI:10.1007/BF00321104

PMID:3779113

Abstract

摘要

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Type I and type II disease in congenital factor XIII deficiency. A further demonstration of the correctness of the classification.先天性因子 XIII 缺乏症中的 I 型和 II 型疾病。分类正确性的进一步证明。

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引用本文的文献

Successful pregnancy in a woman with congenital factor XIII deficiency treated with substitutive therapy. Report of a second case.接受替代疗法治疗的先天性因子 XIII 缺乏症女性成功妊娠。第二例报告。

Blut. 1987 Jul;55(1):45-8. doi: 10.1007/BF00319641.

本文引用的文献

A hitherto undescribed congenital haemorrhagic diathesis probably due to fibrin stabilizing factor deficiency.一种迄今未被描述的先天性出血素质，可能是由于纤维蛋白稳定因子缺乏所致。

Thromb Diath Haemorrh. 1960 Dec 15;5:179-86.

An electrophoretic and quantitative analysis of coagulation factor XIII in normal and deficient subjects.正常受试者和凝血因子 XIII 缺乏受试者中凝血因子 XIII 的电泳及定量分析。

Br J Haematol. 1980 Aug;45(4):633-40. doi: 10.1111/j.1365-2141.1980.tb07186.x.

Hereditary factor XIII deficiency: report of four families and definition of the carrier state.

Br J Haematol. 1984 Mar;56(3):495-505. doi: 10.1111/j.1365-2141.1984.tb03979.x.

Factor XIII levels in five families of patients with inherited factor XIII deficiency: support for an autosomal recessive inheritance.五例遗传性因子 XIII 缺乏症患者家族中的因子 XIII 水平：支持常染色体隐性遗传

Thromb Haemost. 1983 Aug 30;50(2):588-90.

Factor XIII deficiency associated with Klippel-Weber disease, platelet dysfunction and cryofibrinogenemia.与克-韦二氏病、血小板功能障碍和冷纤维蛋白原血症相关的凝血因子XIII缺乏症

Acta Haematol. 1983;69(6):398-403. doi: 10.1159/000206928.

[Presence of a plasma antigen indispensable to the stabilization of fibrin in 2 cases on congenital factor XIII deficiency].[2例先天性因子XIII缺乏症患者中存在对纤维蛋白稳定必不可少的血浆抗原]

Thromb Diath Haemorrh. 1970 Dec 31;24(3):356-60.

[2 patients with congenital factor XIII deficiency. Contribution to the problem of factor XIII determination].[2例先天性因子XIII缺乏症患者。对因子XIII测定问题的贡献]

Thromb Diath Haemorrh. 1970 May 31;23(2):313-39.

Demonstration of factor XIII in human megakaryocytes by a fluorescent antibody technique.应用荧光抗体技术在人巨核细胞中证实因子ⅩⅢ

Ann N Y Acad Sci. 1972 Dec 8;202:318-28. doi: 10.1111/j.1749-6632.1972.tb16344.x.

Documentation of the plasma factor XIII deficiency in man.人类血浆凝血因子 XIII 缺乏症的记录。

Ann N Y Acad Sci. 1972 Dec 8;202:190-9. doi: 10.1111/j.1749-6632.1972.tb16331.x.

Immunological studies of coagulation factor XIII.凝血因子 XIII 的免疫学研究。

J Clin Invest. 1973 Oct;52(10):2398-403. doi: 10.1172/JCI107429.

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