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Journal Abstract Search
121 related items for PubMed ID: 5708123
1. Studies on a family with dysfibrinogenemia. Mammen EF, Prasad AS, Au CC. Thromb Diath Haemorrh; 1968 Jul 31; 19(3):03-4. PubMed ID: 5708123 [No Abstract] [Full Text] [Related]
2. Isolation and characterization of the clottable low molecular weight fibrinogen derived by limited plasmin hydrolysis of human fraction I-4. Sherman LA, Mosesson MW, Sherry S. Biochemistry; 1969 Apr 31; 8(4):1515-23. PubMed ID: 4241001 [No Abstract] [Full Text] [Related]
3. 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]
9. Congenital dysfibrinogenemia: fibrinogen Detroit. Mammen EF, Prasad AS, Barnhart MI, Au CC. J Clin Invest; 1969 Feb 30; 48(2):235-49. PubMed ID: 4974308 [Abstract] [Full Text] [Related]
10. Human chorionic gonadotropin. I. Purification and physicochemical properties. Bahl OP. J Biol Chem; 1969 Feb 25; 244(4):567-74. PubMed ID: 5768856 [No Abstract] [Full Text] [Related]
11. Congenital hypofibrinogenemia and recurrent placental abruption. Ness PM, Budzynski AZ, Olexa SA, Rodvien R. Obstet Gynecol; 1983 Apr 25; 61(4):519-23. PubMed ID: 6828283 [Abstract] [Full Text] [Related]
12. Fibrinogen Poissy II (gammaN361K): a novel dysfibrinogenemia associated with defective polymerization and peptide B release. Mathonnet F, Guillon L, Detruit H, Mazmanian GM, Dreyfus M, Alvarez JC, Giudicelli Y, de Mazancourt P. Blood Coagul Fibrinolysis; 2003 Apr 25; 14(3):293-8. PubMed ID: 12695754 [Abstract] [Full Text] [Related]
13. 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]
15. [Dysfibrinogenemia]. Philippe N. Pediatrie; 1972 Apr 31; 27(1):93-100. PubMed ID: 4557225 [No Abstract] [Full Text] [Related]
16. Bovine fibrinogen--heterogeneity of the gamma-chains. Gerbeck CM, Yoshikawa T, Montgomery R. Arch Biochem Biophys; 1969 Oct 31; 134(1):67-75. PubMed ID: 5388090 [No Abstract] [Full Text] [Related]
17. Congenital afibrinogenemia. A case report with some considerations on the hereditary transmission of this disorder. Girolami A, Zacchelo G, D'Elia R. Thromb Diath Haemorrh; 1971 Jun 30; 25(3):460-8. PubMed ID: 5561958 [No Abstract] [Full Text] [Related]
18. Isolation and characterization of human Factor VIII (antihemophilic factor). Legaz ME, Schmer G, Counts RB, Davie EW. J Biol Chem; 1973 Jun 10; 248(11):3946-55. PubMed ID: 4708094 [No Abstract] [Full Text] [Related]
19. [A new case of Congenital and familial dysfibrinogenemia without Hemorrhagic Diathesis]. Streiff F, Alexandre P, Vigneron C, Soria J, Soria C, Mester L. Thromb Diath Haemorrh; 1971 Dec 31; 26(3):565-76. PubMed ID: 4947421 [No Abstract] [Full Text] [Related]
20. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen. Haverkate F, Samama M. Thromb Haemost; 1995 Jan 31; 73(1):151-61. PubMed ID: 7740487 [Abstract] [Full Text] [Related] Page: [Next] [New Search]