Zobrazeno 1 - 10
of 138
pro vyhledávání: '"E E Ohnhaus"'
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 108:905-908
The toxic shock syndrome was observed in two young men (16 and 22 years). In one it occurred after a purulent scraping wound of the skin, in the other two days after an operation with seemingly normal wound conditions. All findings returned to normal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07263b845865fbce37b7d1250dc54d2a
https://doi.org/10.1055/s-2008-1069665
https://doi.org/10.1055/s-2008-1069665
Autor:
Michael Mayersohn, K. Stoeckel, Theodor W. Guentert, E. E. Ohnhaus, J. P. Pfefen, C. Andressen, M. P. Schoerlin, Felix J. Frey
Publikováno v:
Acta Psychiatrica Scandinavica. 82:94-97
Three different studies were conducted to assess the pharmacokinetics of moclobemide in subjects with conditions complicating dose determination. The first examined the absorption and disposition of moclobemide in an elderly population and compared t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a07f8690a557a3a4b8fab932e7d9e418
https://doi.org/10.1111/j.1600-0447.1990.tb05346.x
https://doi.org/10.1111/j.1600-0447.1990.tb05346.x
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 24(10)
The calcium channel blocker nifedipine is metabolized by cytochrome P450 3A4, which is present in liver and mucosa of the small bowel. Cytochrome P450 3A4 is inducible by the tuberculostatic rifampin in liver and the small bowel. The contribution of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4453705ef957390fd5839f65d7436736
https://pubmed.ncbi.nlm.nih.gov/9311630
https://pubmed.ncbi.nlm.nih.gov/9311630
Publikováno v:
International journal of clinical pharmacology, therapy, and toxicology. 28(9)
The pharmacokinetics of nitrazepam and temazepam were investigated in 16 healthy volunteers before and after seven days of the administration of rifampin 600 mg/d and/or probenecid 500 mg/d. In order to determine the endoplasmatic reticulum enzyme fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e5079be6b5ff969d81cb68f073135073
https://pubmed.ncbi.nlm.nih.gov/2228325
https://pubmed.ncbi.nlm.nih.gov/2228325
Publikováno v:
The Journal of Clinical Pharmacology. 23:171-177
The pharmacokinetics of atenolol were investigated following single intravenous (25 mg) and oral administration (100 mg) of atenolol in 13 patients with chronic liver disease and normal renal function and in 12 normal healthy volunteers. Four of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::142f1bca2f6ec824f8721b0b0b830c11
https://doi.org/10.1002/j.1552-4604.1983.tb02721.x
https://doi.org/10.1002/j.1552-4604.1983.tb02721.x
Publikováno v:
Clinical Pharmacology & Therapeutics. 25:591-597
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e9c34242d03f4bb0daac351e1112532
https://doi.org/10.1002/cpt1979255part1591
https://doi.org/10.1002/cpt1979255part1591
Publikováno v:
European Journal of Clinical Pharmacology. 22:423-428
Increased metabolism of pindolol in renal impairment has previously been suggested by pharmacokinetic calculations. The present study was a pharmacokinetic and metabolic investigation in 7 patients with severe renal impairment (endogeneous creatinine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c65734ef9475a3268faaf29ef32eacf
https://doi.org/10.1007/bf00542547
https://doi.org/10.1007/bf00542547
Publikováno v:
Clinical Pharmacokinetics. 13:110-117
The pharmacokinetics of bisoprolol were investigated following oral administration of 10mg once daily for 7 days in 8 healthy subjects, in 14 patients with different degrees of renal impairment and in 18 patients with liver disease. In healthy subjec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ba4ed4bc902f9fba138bfc3cde234cf
https://doi.org/10.2165/00003088-198713020-00003
https://doi.org/10.2165/00003088-198713020-00003
Publikováno v:
Therapeutic Drug Monitoring. 11:411-414
The pharmacokinetic interaction between the gastrointestinal motility-stimulating substance cisapride and the H2-antagonist cimetidine was examined in 8 healthy volunteers (25 +/- 2 years of age). Steady-state kinetics of both substances were investi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20e5958bb0ec790ea5617faceb8a343f
https://doi.org/10.1097/00007691-198907000-00007
https://doi.org/10.1097/00007691-198907000-00007
Publikováno v:
Rinsho yakuri/Japanese Journal of Clinical Pharmacology and Therapeutics. 19:767-772
Although there are some reports which state that phenacetin is unlikely to be theprimary causative agent in analgesic nephropathy (Prescott, 1982), 80% of the 285phenacetin abusers observed in our clinic between 1962 and 1979 were suffering fromchron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc13c9a1f172a58bf88ff063e8e09c5d
https://doi.org/10.3999/jscpt.19.767
https://doi.org/10.3999/jscpt.19.767