Zobrazeno 1 - 10
of 12
pro vyhledávání: '"J. D. Nagel"'
Publikováno v:
Cancer Chemotherapy and Pharmacology. 29:480-484
The pharmacokinetics of intraperitoneally (i.p.) injected mitoxantrone was determined in plasma and peritoneal dialysate taken from five patients presenting with cancer confined to the peritoneal cavity over a sampling period of 1 week. The drug was
Publikováno v:
Cancer Chemotherapy and Pharmacology. 27:121-124
A new tumour model that is particularly suitable for testing intraperitoneal chemotherapy is described. Single tumours were induced to grow in the mesentery of rats by the implantation of small pieces taken from subcutaneous tumours. Tumour growth wa
Publikováno v:
Klinische Padiatrie. 209(6)
Mitochondrial disease are a heterogeneous group, combining multiple symptoms resulting from defects in various organs. Thus identification of a particular mitochondrial disease due to clinical symptoms is not possible. However, simple biochemical tes
Autor:
J D, Nagel
Publikováno v:
Maryland medical journal (Baltimore, Md. : 1985). 40(5)
Publikováno v:
Cancer chemotherapy and pharmacology. 29(2)
The clinical pharmacokinetics of mitoxantrone in hyperthermic, isolated perfusion of the leg were studied in five patients exhibiting solitary, localized malignant melanoma. Mitoxantrone was given as four 1-min infusions at 15-min intervals into the
Publikováno v:
Selective cancer therapeutics. 6(2)
Tumor growth was studied in a peritoneal tumor model in the rat after intravenous and intraperitoneal administration of doxorubicin (4 mg/kg), mitoxantrone (2.5 mg/kg) and cisplatin (4 mg/kg) and after intraperitoneal administration of carboplatin (2
Autor:
A. U. Bandhoe, A. C. A. Paalman, W. J. M. Underberg, J. H. Beijnen, O. Bekers, M. Otagiri, A. Bult, Gert Beuman, Jacques van der Heijden, Jenny Janss, P. R. J. Ceelen, G. G. L. M. Feenstra-Bielders, D. J. Groeneveld, D. de Boer, M. J. A. Rutten, E. G. de Jong, R. A. A. Maes, J. M. van Rossum, G. de Groot, R. Kopps, T. J. F. Savelkoul, P. van Vloten, E. G. de Jonag, R. van Ooyen, J. Kiffers, I. F. I. de Kroon, P. N. J. Langendijk, P. N. F. C. de Goede, M. De Smet, C. Musch, A. Peeters, L. Buydens, D. L. Massart, K. De Turck, Th. Cachet, J. Hoogmartens, M. Delrue, P. Lannoo, B. F. H. Drenth, F. J. Beckeringh, J. Bosman, K. G. Feitsma, A. van Nijhuisvan Dam, R. J. Driebergen, J. A. van Gorp, K. Ensing, A. Farlam, G. J. de Jong, R. W. Frel, U. A. Th. Brinkman, T. K. Gerding, V. J. M. van de Grampel, N. R. Niemeijer, R. A. de Zeeuw, P. G. Tepper, A. S. Horn, J. J. Halvax, G. Wiese, W. P. van Bennekom, Rik Hindriks, Lutgarde Buydens, Anne Peeters, Marina de Smet, Luc Massart, Aric Blokland, Jan Vink, S. Keizers, W. M. A. Niessen, E. R. Verhey, G. F. LaVos, U. R. Tjaden, J. van der Greef, J. A. Ooms, G. S. J. Haak, G. Grooten, G. Pattyn, P. Sandra, F. David, A. T. van Oosterom, E. A. de Bruijn, A. V. Pouwelse, D. de Jong, N. G. F. M. Lammers, J. H. M. van den Berg, I. Quintens, E. Roets, H. J. E. M. Reeuwijk, H. Lingeman, H. J. Keizer, H. Rosing, F. Elferink, F. J. van de Vaart, P. H. A. M. Kloeg, André Sauter, D. S. Stegehuis, N. J. Reinhoud, O. M. Steijger, J. J. L. Hilhorst, J. J. M. Holthuis, U. K. Underberg-Chitoe, P. L. Meenhorst, G. Van den Mooter, R. Hauchecorne, C. Vinckier, A. van der Horst, H. J. M. Martens, F. A. L. van der Horst, M. H. Post, L. A. van Ginkel, P. W. Zoontjes, H. van Blitterswijk, R. W. Stephany, R. van Gijn, C. H. Bakker, C. H. W. Koks, S. Rodenhuis, M. A. J. van Opstal, F. A. L. van den Horst, P. Krabbenborg, O. van Tellingen, H. R. v. d. Woude, C. J. T. van Beers, W. J. Nooyen, F. J. Varossieau, G. Los, J. D. Nagel, J. G. McVie, R. N. Veen, J. T. Op 't Land, D. E. M. M. Vendrig, J. Teeuwsen, F. C. A. M. Verlaar, T. J. H. M. Trum, J. P. de Kleijn, R. Vervoort, M. Vrieling, F. Maris, H. Hindriks, A. Walhagen, L. -E. Edholm, C. E. M. Heeremans, R. A. M. van der Hoeven
Publikováno v:
Pharmaceutisch Weekblad. 11:A1-A14
Publikováno v:
Laboratory animals. 23(3)
A new method of sampling ascitic fluid from rats over a period of at least 8 h in a reliable and easy way is described. The objective was to determine drug concentrations in ascitic fluid after intraperitoneal chemotherapy. Two silicon tubes were imp
Publikováno v:
Clinicalexperimental metastasis. 7(4)
Injection of 1 x 10(6) CC531 colonic carcinoma cells into the mesenteric lymph nodes of Wag/Rij rats resulted in the growth of tumors within the lymph nodes. These were apparent after 3 days, whereas lung and liver metastases were not observed until
Autor:
J D, NAGEL
Publikováno v:
New York state journal of medicine. 54(2)