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相似文献
1
[Fibrinogenopathies].[纤维蛋白原病]
Acta Haematol Pol. 1972 Jan-Mar;3(1):93-9.
2
[Dysfibrinogemia (literature survey)].[异常纤维蛋白原血症（文献综述）]
Lab Delo. 1974;8(0):451-5.
3
Coagulation studies in a case of severe congenital hypofibrinogenemia.一例严重先天性低纤维蛋白原血症的凝血研究
Thromb Diath Haemorrh. 1972 Aug 31;28(1):129-34.
4
Fibrinogen Troyes--fibrinogen Metz. Two new cases of congenital dysfibrinogenemia.纤维蛋白原特鲁瓦——纤维蛋白原梅斯。两例先天性异常纤维蛋白原血症新病例。
Thromb Diath Haemorrh. 1972 Jul 31;27(3):619-33.
5
A new congenital abnormality of human fibrinogen. Fibrinogen Bethesda II.一种新的人类纤维蛋白原先天性异常。纤维蛋白原贝塞斯达II型。
Thromb Diath Haemorrh. 1973 Jun 28;29(3):562-71.
6
Differential diagnosis of acquired hypofibrinogenemias, part I.获得性纤维蛋白原减少症的鉴别诊断，第一部分。
Curr Surg. 1982 Jul-Aug;39(4):226-43.
7
[Defective structure of the thrombus and inhibition of thrombus formation in defibrination hemorrhages caused by non-clottable fibrinogen derivatives].[去纤维蛋白原性出血中血栓的结构缺陷及不可凝纤维蛋白原衍生物对血栓形成的抑制作用]
Thromb Diath Haemorrh. 1967 May 31;17(3-4):543-51.
8
[Familial dysfibrinogenemia with abnormal nonomer aggregation. Paris III fibrinogen].
Pathol Biol (Paris). 1974 Nov;22 suppl:72-9.
9
[A new case of dysfibrinogenemia].
Klin Wochenschr. 1971 Jul 15;49(14):806-8. doi: 10.1007/BF01496424.
10
[Blood coagulation disorders caused by genetic variants of fibrinogen].[纤维蛋白原基因变异引起的血液凝固障碍]
Z Arztl Fortbild (Jena). 1970 Sep 15;64(18):913-8.
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