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24. Coagulation studies in a case of severe congenital hypofibrinogenemia. Barbu T, Porciello PI, Dini E. Thromb Diath Haemorrh; 1972 Aug 31; 28(1):129-34. PubMed ID: 4627565 [No Abstract] [Full Text] [Related]
28. [Function of thrombocytes in hemorrhagic diathesis, thrombosis and vascular diseases]. Breddin K. Thromb Diath Haemorrh Suppl; 1968 Aug 31; 27():1-200. PubMed ID: 5761078 [No Abstract] [Full Text] [Related]
29. Inherited fibrinolytic disorder due to an enhanced plasminogen activator level. Aznar J, Estellés A, Vila V, Regañón E, España F, Villa P. Thromb Haemost; 1984 Oct 31; 52(2):196-200. PubMed ID: 6543037 [Abstract] [Full Text] [Related]
31. Fibrinogen Troyes--fibrinogen Metz. Two new cases of congenital dysfibrinogenemia. Soria J, Soria C, Samama M, Poirot E, Kling C. Thromb Diath Haemorrh; 1972 Jul 31; 27(3):619-33. PubMed ID: 4662617 [No Abstract] [Full Text] [Related]
37. Absent plasma second phase platelet aggregation factor in a patient with Hageman trait. Okonkwo P, Post R, Sise H. Thromb Diath Haemorrh; 1970 Jun 30; 23(3):423-31. PubMed ID: 5432187 [No Abstract] [Full Text] [Related]