Authors:
Briasoulis, E
Judson, I
Pavlidis, N
Beale, P
Wanders, J
Groot, Y
Veerman, G
Schuessler, M
Niebch, G
Siamopoulos, K
Tzamakou, E
Rammou, D
Wolf, L
Walker, R
Hanauske, A
Citation: E. Briasoulis et al., Phase I trial of 6-hour infusion of glufosfamide, a new alkylating agent with potentially enhanced selectivity for tumors that overexpress transmembrane glucose transporters: A study of the European Organization for Researchand Treatment of Cancer Early Clinical Studies Group, J CL ONCOL, 18(20), 2000, pp. 3535-3544
Authors:
Nagaraja, NV
Pechstein, B
Erb, K
Klipping, C
Hermann, R
Niebch, G
Derendorf, H
Citation: Nv. Nagaraja et al., Pharmacokinetic and pharmacodynamic modeling of cetrorelix, an LH-RH antagonist, after subcutaneous administration in healthy premenopausal women, CLIN PHARM, 68(6), 2000, pp. 617-625
Authors:
Breithaupt-Grogler, K
Niebch, G
Schneider, E
Erb, K
Hermann, R
Blume, HH
Schug, BS
Belz, GG
Citation: K. Breithaupt-grogler et al., Dose-proportionality of oral thioctic acid - coincidence of assessments via pooled plasma and individual data, EUR J PH SC, 8(1), 1999, pp. 57-65
Authors:
Duijkers, IJM
Klipping, C
Willemsen, WNP
Krone, D
Schneider, E
Niebch, G
Hermann, R
Citation: Ijm. Duijkers et al., Single and multiple dose pharmacokinetics and pharmacodynamics of the gonadotrophin-releasing hormone antagonist Cetrorelix in healthy female volunteers, HUM REPR, 13(9), 1998, pp. 2392-2398