Zobrazeno 1 - 10
of 36
pro vyhledávání: 'Lüllmann-Rauch, Renate'
Autor:
Renate Lüllmann-Rauch, Stefan H. Geist
Publikováno v:
Annals of Anatomy - Anatomischer Anzeiger. 176:3-9
Summary The purpose of this study was to investigate the effects of two lipidosis-inducing drugs (the anorectic drug chlorphentermine and the tricyclic antidepressantimipramine) upon the estrous cycle of rats and upon the morphology of the vaginal an
Autor:
Lüllmann-Rauch, Renate
Publikováno v:
Cell & Tissue Research; 1974, Vol. 149 Issue 4, p587-590, 4p
Publikováno v:
Virchows Archiv B Cell Pathology; Mar1976, Vol. 20 Issue 1, p343-346, 4p
Publikováno v:
Cell & Tissue Research; 1976, Vol. 171 Issue 2, p273-276, 4p
Publikováno v:
Virchows Archiv B Cell Pathology; Jun1983, Vol. 43 Issue 1, p309-316, 8p
Publikováno v:
Virchows Archiv B Cell Pathology; Mar1982, Vol. 39 Issue 1, p59-73, 15p
Lipidosislike renal changes in rats treated with chlorphentermine or with tricyclic antidepressants.
Autor:
Lüllmann-Rauch, Renate
Publikováno v:
Virchows Archiv B Cell Pathology; Jun1975, Vol. 18 Issue 1, p51-60, 10p
Autor:
Renate Lüllmann-Rauch
Publikováno v:
Naunyn-Schmiedeberg's Archives of Pharmacology. 286:165-179
Lymphocytes of rat lymph nodes have previously been revealed as reliable and sensitive indicators of a particular drug side effect, notably a generalized phospholipidosis, inducible by a compound of amphiphilic character (chlorphentermine). The purpo
Experimental myopathy induced by amphiphilic cationic compounds including several psychotropic drugs
Autor:
Renate Lüllmann-Rauch, D. Drenckhahn
Publikováno v:
Neuroscience. 4:549-562
Several amphiphilic cationic compounds with different therapeutic actions, among them several psychotropic drugs, which have previously been described as inducing generalized lipidosis, were examined for their myotoxic effects in rats. Chronic admini
Publikováno v:
CRC Critical Reviews in Toxicology. 4:185-218
This review deals with drug-induced lipidoses and the possible underlying mechanisms. A variety of drugs, widely differing in their main pharmacological actions, but closely resembling each other with respect to particular physiochemical properties,