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pro vyhledávání: '"Robert E. Ober"'
Autor:
Robert E. Ober
Publikováno v:
The New England journal of medicine. 235(24)
Publikováno v:
Journal of Pharmaceutical Sciences. 72:236-239
A procedure of direct injection of whole plasma for the analysis of theophylline by an automated multidimensional high-performance liquid chromatographic (HPLC) technique is described. The procedure requires as little as 30 microliters of plasma samp
Publikováno v:
Toxicological Sciences. 4:972-976
Publikováno v:
The Journal of Clinical Pharmacology. 21:401-404
The absorption, biotransformation, and pharmacokinetics of the antiinflammatory drug salicylsalicylic acid (SSA) were studied. Healthy adult males received 1000 mg SSA and 1300 mg aspirin according to a crossover design either as a single oral dose (
Publikováno v:
Fundamental and Applied Toxicology. 4:972-976
After a single intravenous dose of ammonium [14C]perfluorooctanoate [( 14C]PFO, 13.3 mg/kg) or of potassium [14C]perfluorooctanesulfonate [( 14C]PFOS, 3.4 mg/kg) to rats, cholestyramine fed daily as a 4% mixture in feed was shown to increase the tota
Autor:
Robert E. Ober
Publikováno v:
Drug metabolism reviews. 10(2)
Autor:
Lester I. Harrison, Robert E. Ober, Chad S Hansen, Howard L. Miller, Dietrich Schuppan, Mary L. Funk, Stephen R. Rohlflng
Publikováno v:
The Journal of antimicrobial chemotherapy. 15(3)
Plasma and urine concentrations of flumequine and its microbiologically active metabolite, 7-hydroxyflumequine, were determined in healthy subjects following single oral doses of 400, 800, and 1200 mg of flumequine, and following multiple oral doses
Autor:
Robert E. Ober, Gordon J. Conard
Publikováno v:
The American journal of cardiology. 53(5)
After oral administration in healthy human subjects, flecainide absorption is prompt (average peak level at 3 to 4 hours) and nearly complete (at least 90%); flecainide does not appear to undergo consequential presystemic biotransformation. Oral abso
Publikováno v:
Advances in Tracer Methodology ISBN: 9781468486216
The antibiotic paromomycin is a basic, water-soluble compound with a general structure similar to that of neomycin and kanamycin [1]. Failure to obtain radiochemically pure paromomycin following exposure to tritium gas by the Wilzbach technique [2] p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a00fa2864c76b4caa612a9733d57582
https://doi.org/10.1007/978-1-4684-8619-3_12
https://doi.org/10.1007/978-1-4684-8619-3_12