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3. Acquired dysfibrinogenemia secondary to mithramycin toxicity. Ashby MA; Lazarchick J Am J Med Sci; 1986 Jul; 292(1):53-5. PubMed ID: 2940861 [TBL] [Abstract][Full Text] [Related]
4. Fibrinogen date: congenital hypodysfibrinogenemia associated with decreased binding of tissue-plasminogen activator. Ieko M; Sawada K; Sakurama S; Yamagishi I; Isogawa S; Nakagawa S; Satoh M; Yasukouchi T; Matsuda M Am J Hematol; 1991 Aug; 37(4):228-33. PubMed ID: 1830454 [TBL] [Abstract][Full Text] [Related]
5. Subunits and susceptibility of fibrins formed from bovine fibrinogen by arvin, reptilase, thrombin and staphylothrombin. Zajdel M; Wegrzynowicz Z; Sawecka J; Kopeć M Thromb Res; 1975 Apr; 6(4):337-44. PubMed ID: 1169826 [No Abstract] [Full Text] [Related]
11. Fibrinogen Marburg a new genetic variant of fibrinogen. Fuchs G; Egbring R; Havemann K Blut; 1977 Feb; 34(2):107-18. PubMed ID: 836966 [TBL] [Abstract][Full Text] [Related]
12. Fibrinogen Cleveland II. An abnormal fibrinogen with defective release of fibrinopeptide A. Crum ED; Shainoff JR; Graham RC; Ratnoff OD J Clin Invest; 1974 May; 53(5):1308-19. PubMed ID: 4856883 [TBL] [Abstract][Full Text] [Related]
13. Fibrinogen Stony Brook II: partial characterization of a heterozygously transmitted peptide A anomaly. Galanakis DK; Hultin M Blood Coagul Fibrinolysis; 1990 Oct; 1(4-5):567-70. PubMed ID: 2133235 [TBL] [Abstract][Full Text] [Related]
14. Preferential degradation of soluble fibrin monomers in streptokinase-activated plasma. Konttinen YP; Lalla ML; Turunen O Thromb Diath Haemorrh; 1973 Nov; 30(2):403-13. PubMed ID: 4543990 [No Abstract] [Full Text] [Related]
15. Fibrinogen Baltimore II: congenital hypodysfibrinogenemia with delayed release of fibrinopeptide B and decreased rate of fibrinogen synthesis. Ebert RF; Bell WR Proc Natl Acad Sci U S A; 1983 Dec; 80(23):7318-22. PubMed ID: 6580646 [TBL] [Abstract][Full Text] [Related]
16. [Increased thrombin time in a patient with multiple myeloma]. Bohler A; Redondo M; Lämmle B Ther Umsch; 1999 Sep; 56(9):491-4. PubMed ID: 10517116 [TBL] [Abstract][Full Text] [Related]
17. Dysfibrinogenaemia associated with a defect in the aggregation of the fibrin monomers (Almeria I fibrinogen). A preliminary study. Vila V; Regañon E; Fernandez-Pavon A; Aznar J Scand J Haematol; 1984 Nov; 33(5):460-5. PubMed ID: 6515329 [TBL] [Abstract][Full Text] [Related]
19. A novel natural mutation AαPhe98Ile in the fibrinogen coiled-coil affects fibrinogen function. Riedelová-Reicheltová Z; Kotlín R; Suttnar J; Geierová V; Riedel T; Májek P; Dyr JE Thromb Haemost; 2014 Jan; 111(1):79-87. PubMed ID: 24108601 [TBL] [Abstract][Full Text] [Related]
20. Differences in the function and secretion of congenital aberrant fibrinogenemia between heterozygous γD320G (Okayama II) and γΔN319-ΔD320 (Otsu I). Mukai S; Ikeda M; Takezawa Y; Sugano M; Honda T; Okumura N Thromb Res; 2015 Dec; 136(6):1318-24. PubMed ID: 26573395 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]