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Results: 1-9 |
Results: 9
Prophylactic therapy with enoxaparin during L-asparaginase treatment in children with acute lymphoblastic leukemia
Authors: Elhasid, R Lanir, N Sharon, R Ben Arush, MW Levin, C Postovsky, S Ben Barak, A Brenner, B
Citation: R. Elhasid et al., Prophylactic therapy with enoxaparin during L-asparaginase treatment in children with acute lymphoblastic leukemia, BL COAG FIB, 12(5), 2001, pp. 367-370
Acquired activated protein C resistance is common in cancer patients and is associated with venous thromboembolism
Authors: Haim, N Lanir, N Hoffman, R Haim, A Tsalik, M Brenner, B
Citation: N. Haim et al., Acquired activated protein C resistance is common in cancer patients and is associated with venous thromboembolism, AM J MED, 110(2), 2001, pp. 91-96
The effect of thrombophylaxis on pregnancy outcome in patients with recurrent pregnancy loss associated with factor V Leiden mutation
Authors: Younis, JS Ohel, G Brenner, B Haddad, S Lanir, N Ben-Ami, M
Citation: Js. Younis et al., The effect of thrombophylaxis on pregnancy outcome in patients with recurrent pregnancy loss associated with factor V Leiden mutation, BR J OBST G, 107(3), 2000, pp. 415-419
Activated protein C resistance and factor V Leiden mutation can be associated with first- as well as second-trimester recurrent pregnancy loss
Authors: Younis, JS Brenner, B Ohel, G Tal, J Lanir, N Ben-Ami, M
Citation: Js. Younis et al., Activated protein C resistance and factor V Leiden mutation can be associated with first- as well as second-trimester recurrent pregnancy loss, AM J REPROD, 43(1), 2000, pp. 31-35
Molecular analysis of the genotype-phenotype relationship in factor VII deficiency
Authors: Millar, DS Kemball-Cook, G McVey, JH Tuddenham, EGD Mumford, AD Attock, GB Reverter, JC Lanir, N Parapia, LA Reynaud, J Meili, E von Felton, A Martinowitz, U Prangnell, DR Krawczak, M Cooper, DN
Citation: Ds. Millar et al., Molecular analysis of the genotype-phenotype relationship in factor VII deficiency, HUM GENET, 107(4), 2000, pp. 327-342
Multiple retinal arteriolar occlusions associated with coexisting primary antiphospholipid syndrome and factor V Leiden mutation
Authors: Dori, D Beiran, I Gelfand, Y Lanir, N Scharf, J Miller, B Brenner, B
Citation: D. Dori et al., Multiple retinal arteriolar occlusions associated with coexisting primary antiphospholipid syndrome and factor V Leiden mutation, AM J OPHTH, 129(1), 2000, pp. 106-108
Budd-Chiari syndrome associated with factor V Leiden mutation: A report of6 patients
Authors: Hoffman, R Nimer, A Lanir, N Brenner, B Baruch, Y
Citation: R. Hoffman et al., Budd-Chiari syndrome associated with factor V Leiden mutation: A report of6 patients, LIVER TR S, 5(2), 1999, pp. 96-100
Thrombophilic polymorphisms are common in women with fetal loss without apparent cause
Authors: Brenner, B Sarig, G Weiner, Z Younis, J Blumenfeld, Z Lanir, N
Citation: B. Brenner et al., Thrombophilic polymorphisms are common in women with fetal loss without apparent cause, THROMB HAEM, 82(1), 1999, pp. 6-9
A missense mutation in gamma-glutamyl carboxylase gene causes combined deficiency of all vitamin K-dependent blood coagulation factors
Authors: Brenner, B Sanchez-Vega, B Wu, SM Lanir, N Stafford, DV Solera, J
Citation: B. Brenner et al., A missense mutation in gamma-glutamyl carboxylase gene causes combined deficiency of all vitamin K-dependent blood coagulation factors, BLOOD, 92(12), 1998, pp. 4554-4559
Risultati: 1-9 |