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Results: 1-3 |
Results: 3
Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies
Authors: Tirado, I Mateo, J Soria, JM Oliver, A Borrell, M Coll, I Vallve, C Souto, JC Martinez-Sanchez, E Fontcuberta, J
Citation: I. Tirado et al., Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies, HAEMATOLOG, 86(11), 2001, pp. 1200-1208
A boy with venous thrombosis, homozygous for factor V Leiden, prothrombin G20210A and MTHFR C667T mutations, but belonging to an asymptomatic family
Authors: Soria, JM Quintana, R Vallve, C Iruin, G Cortes, C Fontcuberta, J
Citation: Jm. Soria et al., A boy with venous thrombosis, homozygous for factor V Leiden, prothrombin G20210A and MTHFR C667T mutations, but belonging to an asymptomatic family, HAEMATOLOG, 85(11), 2000, pp. 1230-1232
Topical heparin for the treatment of acute superficial phlebitis secondaryto indwelling intravenous catheter - A double-blind, randomized, placebo-controlled trial
Authors: Vilardell, M Sabat, D Arnaiz, JA Bleda, MJ Castel, JM Laporte, JR Vallve, C
Citation: M. Vilardell et al., Topical heparin for the treatment of acute superficial phlebitis secondaryto indwelling intravenous catheter - A double-blind, randomized, placebo-controlled trial, EUR J CL PH, 54(12), 1999, pp. 917-921
Risultati: 1-3 |