Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Mats Ehrnebo"'
Autor:
Filip Bergquist, Mats Ehrnebo, Dag Nyholm, Anders Johansson, Fredrik Lundin, Per Odin, Per Svenningsson, Fredrik Hansson, Leif Bring, Elias Eriksson, Nil Dizdar
Background and ObjectivesIntestinal levodopa/carbidopa gel infusion (LCIG) is superior to oral treatment in advanced Parkinson disease. The primary objective of this trial was to investigate whether continuous subcutaneous or intravenous infusion wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19e71ca890f43fd24020a2b629ab6c1e
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-188600
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-188600
Autor:
Cecilia Gomes-Trolin, Tommy Lewander, Dag Nyholm, Sten-Magnus Aquilonius, Tobias Bäckström, Georgios Panagiotidis, Christer Nyström, Mats Ehrnebo
Publikováno v:
Clinical Neuropharmacology. 35:111-117
Objectives To compare bioavailability and pharmacokinetics of single doses of 3 different levodopa formulations given orally in healthy volunteers. Two marketed formulations, standard levodopa/carbidopa, 100/25 mg (LC-100), and dispersible levodopa/b
Autor:
Stavros Gravas, Mats Ehrnebo, Pilar Laguna, Lennart Wagrell, Jean J.M.C.H. de la Rosette, Anders Mattiasson
Publikováno v:
Journal of urology, 174(3), 1002-1006. Elsevier Inc.
PURPOSE: We compared ProstaLund Feedback Treatment (PLFT) to transurethral prostate resection (TURP) in terms of efficacy and safety in a pooled analysis of 3 clinical studies with 1-year followup. MATERIALS AND METHODS: Overall raw data on 183 patie
Publikováno v:
Clinical Pharmacology & Therapeutics. 23:329-337
Fluoride (3 mg) was administered as a continous intravenous infusion during 30 min to 6 healthy subjects. Plasma concentrations and urinary excretion of fluoride in these experiments were compared with those obtained following oral administration of
Autor:
Mats Ehrnebo, Jan Ekstrand
Publikováno v:
Caries Research. 14:96-102
The bioavailability of fluoride (F) from NaF and Na2PO3F dentifrices was studied in detail in young volunteers. The method used was based on a comparison of plasma and urinary data obtained following intravenous administration of a single 3-mg dose F
Publikováno v:
Clinical Pharmacology & Therapeutics. 16:424-429
The binding of pentazocine to human whole blood, plasma, and blood cells was investigated in 20 normal subjects and 22 patients by means of equilibrium dialysis. Plasma protein binding was 56% to 66% in the control sub;ects and 48% to 75% in the pati
Publikováno v:
Clinical Pharmacology & Therapeutics. 22:888-892
The bioavailability of oral pentazocine was studied in 5 healthy volunteers. Plasma concentrations were determined from 30 min up to 6 hr following oral administration (two 50-mg tablets) and, at other occasions, after intravenous injection of 30 mg
Publikováno v:
European Journal of Clinical Pharmacology. 18:189-194
Five healthy subjects were each given fluoride 3.0 mg (F) as sodium fluoride tablets on two occasions - during production of acid urine, induced by giving NH4Cl, and during production of alkaline urine obtained by giving NaHCO3. Frequent plasma and u
Publikováno v:
Psychopharmacology. 76:44-47
Sulpiride (100 mg) was administered intravenously and orally to healthy human subjects. Serum concentrations of sulpiride and prolactin were followed for 36 h. Both routes of drug administration resulted in a pronounced and sustained increase in seru
Publikováno v:
Journal of pharmacokinetics and biopharmaceutics. 7(5)
Five healthy fasting male subjects were each given single doses of intravenous ampicillin (471 mg), oral ampicillin tablets (495 mg), oral bacampicillin hydrochloride tablets (562 mg ampicillin equivalent), and oral pivampicillin hydrochloride capsul