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Autor:
Ben W.J. Mol, H.P. van Geijn, Johannes J. Duvekot, Hans Wolf, Johannes Erwich, R. de Heus, L. Harmark, Myriam Hanssens, Wilfried Gyselaers, Gerard H. A. Visser, C.D. van Holsbeke, F.F.A.M. Schobben
Publikováno v:
The BMJ
British Medical Journal, 338. BMJ Publishing Group
Heus, R, Mol, B W, Erwich, J J, van Geijn, H, Gyselaers, W J, Hanssens, M, Harmark, L, van Holsbeke, C D, Duvekot, J J, Schobben, F F, de Wolf, H & Visser, G H A 2009, ' Adverse drug reactions to tocolytic treatment for preterm labour: prospective cohort study ', British Medical Journal, vol. 338, no. b744, pp. 758-760 .
BMJ (Clinical research ed.), 338. British Medical Association
British Medical Journal, 338(b744), 758-760
British Medical Journal, 338(52):744. BMJ PUBLISHING GROUP
British Medical Journal, 338. BMJ Publishing Group
Heus, R, Mol, B W, Erwich, J J, van Geijn, H, Gyselaers, W J, Hanssens, M, Harmark, L, van Holsbeke, C D, Duvekot, J J, Schobben, F F, de Wolf, H & Visser, G H A 2009, ' Adverse drug reactions to tocolytic treatment for preterm labour: prospective cohort study ', British Medical Journal, vol. 338, no. b744, pp. 758-760 .
BMJ (Clinical research ed.), 338. British Medical Association
British Medical Journal, 338(b744), 758-760
British Medical Journal, 338(52):744. BMJ PUBLISHING GROUP
Objective To evaluate the incidence of serious maternal complications after the use of various tocolytic drugs for the treatment of preterm labour in routine clinical situations.Design Prospective cohort study.Setting 28 hospitals in the Netherlands