| 1. |
Weitz, J. I. (1997) Low-molecular-weight heparin. N. Engl. J. Med.
337, 688–698.
|
| |
| 2. |
Mousa, S. A. and Fareed, J. W. (2001) Advances in anticoagulant, antithrombotic and thrombolytic drugs. Exp. Opin. Invest. Drugs
10(1), 157–162.
|
| |
| 3. |
Fegan, C. D. (1998) Tinzaparin as an antithrombotic: an overview. Hosp. Med.
149, 1285–1288.
|
| |
| 4. |
Aguilar, D. and Goldhaber, S. Z. (1999) Clinical uses of low molecular weight heparin. Chest
115(5), 1418–1423.
|
| |
| 5. |
Linhardt, R. J. and Gunay, N. S. (1999) Production and chemical processing of low molecular weight heparins. Semin. Thromb. Hemost.
25(3), 5–16.
|
| |
| 6. |
Mousa, S. A. (2000) Comparative efficacy among different low molecular weight heparin (LMWHs) & drug interaction: implications
in the management of vascular disorders. Thromb. Haemostasis
26(l)(Suppl. 1), 39–46. This study provides a comparative total anticoagulant efficacy among different LMWH showing dependency on the molecular
weight and degree of sulfation.
|
| |
| 7. |
Hull, R. D., Raskob, G. E., Pineo, G. F., Green, D., Towbridge, A. A., Elliott, C. G, et al. (1992) Subcutaneous low-molecular
weight heparin compared with continuous intravenous heparin in the treatment of proximal-vein thrombosis. N. Engl. J. Med.
326, 975–982. This is a key double-blind clinical trial comparing the efficacy and safety of LMWH to UFH in-patients with VTE.
|
| |
| 8. |
Simonneau, G., Sors, H., Charbonnier, B., Page, Y., Laaban, J.-P., Bosson, J.-L., et al. (1997) A comparison of low-molecular-weight
heparin with unfractionated heparin for acute pulmonary embolism. N. Engl. J. Med.
337, 663–669.
|
| |
| 9. |
Hull, R. D., Raskob, G E., Pineo, G F., Rosenbloom, D., Evans, W., Mallory, T., et al. (1993) A comparison of subcutaneous
low-molecular weight heparin with warfarin sodium for prophylaxis against deep-vein thrombosis after hip or knee implantation.
N. Engl. J. Med.
329, 1370–1376.
|
| |
| 10. |
Leizorovicz, A., Picolet, H., Peyrieux, J. C, Boissel, J. P., and the HBPM research group. (1991) Prevention of perioperative
deep vein thrombosis in general surgery: a multicenter double blind study comparing two doses of logiparin and standard heparin.
Br. J. Surg.
78, 412–416.
|
| |
| 11. |
Ryan, K. E., Lane, D. A., Flynn, A., Shepperd, J., Ireland, H. A., and Curtis, J. R. (1991) Dose finding study of a low molecular
weight heparin, tinzaparin, in haemodialysis. Thromb. Haemostasis
66(3), 277–282.
|
| |
| 12. |
Pedersen, P. C, Østergaard, P. B., Hedner, U., Bergqvist, D., and Mätzsch, T. (1991) Pharmacokinetics of low molecular weight
heparin, logiparin, after intravenous and subcutaneous administration to healthy volunteers. Thromb. Res.
61, 477–487.
|
| |
| 13. |
Mätzsch, T., Bergqvist, D., Hedner, U., and Østergaard, P. B. (1987) Effects of an enzymatically depolymerized heparin as
compared with conventional heparin in healthy volunteers. Thromb. Haemostasis
57(1), 97–101.
|
| |
| 14. |
Mousa, S. A., Bozarth, J., Hainer, J., et al. (2001) Pharmacodynamic of tinzaparin following 175 IU/Kg SC administration in
healthy volunteers on plasma TFPI. Thromb. Haemostasis P2299.
|
| |
| 15. |
Emmanuele, R. M. and Fareed, J. (1987) The effect of molecular weight on the bioavailability of heparin. Thromb. Res.
48, 591–596.
|
| |
| 16. |
Brieger, D. and Dawes, J. (1997) Production method affects the pharmacokinetic and ex vivo biological properties of low molecular weight heparins. Thromb. Haemostasis
77(2), 317–322.
|
| |
| 17. |
Mousa, S. A., Bozarth, J., Larnkjaer, A., and Johanson, K. (2000) Vascular effects of heparin molecular weight fractions and
LMWH on the release of TFPI from human endothelial cells. Blood
16(11), 59, 3928.
|
| |
| 18. |
Kaiser, B., Hoppensteadt, D., and Fareed, J. (2000) Tissue factor pathway inhibitor for cardiovascular disorders. Emerging Drugs
5(1), 73–87.
|
| |
| 19. |
Verstraete, M. (1990) Pharmacotherapeutic aspects of unfractionated and low molecular weight heparins. Drugs
40, 498–530.
|
| |
| 20. |
Lindblad, B. (1988) Prophylaxis of postoperative thromboembolism with low dose heparin alone or in combination with dihydroergotamine.
A review. Acta Chir. Scand. Suppl.
543, 31–42.
|
| |
| 21. |
Hull, R., Delmore, T, Carter, C, Hirsh, J., Genton, E., Gent, M., et al. (1982) Adjusted subcutaneous heparin versus warfarin
sodium in the long-term treatment of venous thrombosis. N. Engl. J. Med.
306, 189–194.
|
| |
| 22. |
Hull, R. D., Raskob, G E., Hirsh, J., Jay, R. M., Leclerc, J. R., Geerts, W. H., et al. (1986) Continuous intravenous heparin
compared with intermittent subcutaneous heparin in the initial treatment of proximal-vein thrombosis. N. Engl. J. Med.
315, 1109–1114.
|
| |
| 23. |
Cruickshank, M. K., Levine, M. N., Hirsh, J., Roberts, R., and Siguenza, M. (1991) A standard heparin nomogram for the management
of heparin therapy [see comments]. Arch. Intern. Med.
151, 333–337.
|
| |
| 24. |
Hull, R. D., Raskob, G. E., Rosenbloom, D., Lemaire, J., Pineo, G. F, Baylis, B., et al. (1992) Optimal therapeutic level
of heparin therapy in patients with venous thrombosis. Arch. Intern. Med.
152, 1589–1595.
|
| |
| 25. |
Goldhaber, S. Z. (1996) Thrombolytic therapy for venous thromboembolism, in Disorders of Thrombosis (Hull, R. and Pineo, G. F., eds.), W.B. Saunders Co, pp. 321–328.
|
| |
| 26. |
Gueret, P., Dubourg, O., Ferrier, A., Farcot, J. C, Rigaud, M., and Bourdarias, J. P. (1986) Effects of full-dose heparin
anticoagulation on the development of left ventricular thrombosis in acute transmural myocardial infarction. J. Am. Coll. Cardiol.
8, 419–426.
|
| |
| 27. |
Neri Serneri, G. G, Gensini, G. F, Poggesi, L., Trotta, F, Modesti, P. A., Boddi, M., et al. (1990) Effect of heparin, aspirin,
or alteplase in reduction of myocardial ischaemia in refractory unstable angina (published erratum appears in Lancet 1990
Apr 7;335[8693]:868). Lancet
335, 615–618.
|
| |
| 28. |
Bounameaux, H., Verhaeghe, R., and Verstraete, M. (1986) Thromboembolism and antithrombotic therapy in peripheral arterial
disease. J. Am. Coll. Cardiol.
8, 98B–103B.
|
| |
| 29. |
Matzsch, T., Bergqvist, D., Hedner, U., Nilsson, B., and Ostergaard, P. (1986) Heparin-induced osteoporosis in rats. Thromb. Haemostasis
56, 293–294.
|
| |
| 30. |
Salzman, E. W., Rosenberg, R. D., Smith, M. H., Lindon, J. N., and Favreau, L. (1980) Effect of heparin and heparin fractions
on platelet aggregation. J. Clin. Invest.
65, 64–73.
|
| |
| 31. |
Friedel, H. A. and Balfour, J. A. (1994) Tinzaparin. A review of its pharmacology and clinical potential in the prevention
and treatment of thromboembolic disorders. Drugs
48, 638–660.
|
| |
| 32. |
Padilla, A., Gray, E., Pepper, D. S., and Barrowcliffe, T. W. (1992) Inhibition of thrombin generation by heparin and low
molecular weight (LMW) heparins in the absence and presence of platelet factor 4 (PF4). Br. J. Haematol.
82, 406–413.
|
| |
| 33. |
Fareed, J., Jeske, W., Hoppensteadt, D., Clarizio, R., and Walenga, J. M. (1998) Low-molecular-weight heparins: pharmacological
profile and product differentiation. Am. J. Cardiol.
82, 3L–10L.
|
| |
| 34. |
Boneu, B., Caranobe, C, Cadroy, Y., Dol, F., Gabaig, A. M., Dupouy, D., et al. (1988) Pharmacokinetic studies of standard
unfractionated heparin, and low molecular weight heparins in the rabbit. Semin. Thromb. Hemost.
14, 18–27.
|
| |
| 35. |
Sutor, A. H., Massicotte, P., Leaker, M., Andrew, M. (1997) Heparin therapy in pediatric patients. Semin. Thromb. Hemost.
23, 303–319.
|
| |
| 36. |
Fareedman, M. D. (1996) Low molecular weight heparins: an emerging new class of glycosaminoglycan antithrombotic. J. Clin. Pharmacol.
31, 298–306. Circulation
93, 2212–2245.
|
| |
| 37. |
Fareed, J., Walenga, J. M., Hoppensteadt, D., Huan, X., and Nonn, R. (1989) Biochemical and pharmacological in-equivalence
of low molecular weight heparins. Ann. NY Acad. Sci.
556, 333–353.
|
| |
| 38. |
Lindahl, A. K., Abildgaard, U., and Stokke, G. (1990) Release of extrinsic pathway inhibitor after heparin injection: increased
response in cancer patients. Thromb. Res.
59, 651–656.
|
| |
| 39. |
Larnkjaer, A., Ostergaard, P. B., and Flodgaard, H. J. (1994) Binding of low molecular weight heparin (Tinzaparin sodium)
to bovine endothelial cells in vitro. Thromb. Res.
75, 185–194.
|
| |
| 40. |
Ostergaard, P., Nordfang, O., Petersen, L. C., Valentin, S., and Kristensen, H. (1993) Is tissue factor pathway inhibitor
involved in the antithrombotic effect of heparins? Biochemical considerations. Haemostasis
23 (Suppl. 1), 107–111.
|
| |
| 41. |
Hull, R. D., Raskob, G E., Rosenbloom, D., Pineo, G., Lerner, R. G, Gafni, A., et al. (1997) Treatment of proximal vein thrombosis
with subcutaneous low-molecular-weight heparin vs. intravenous heparin. Arch. Intern. Med.
157, 289–294.
|
| |