Zobrazeno 1 - 10
of 109
pro vyhledávání: '"G.R. Peters"'
Autor:
NÁDIA F. GARCIA, CAMILA DE MORAES, MACÁRIO A. REBELO, SAVANAH MARIA G.R. PETERS, FÁBIO M.P. DE CASTRO, ENRICO F. PUGGINA
Publikováno v:
Anais da Academia Brasileira de Ciências, Vol 94, Iss suppl 3 (2022)
Abstract Strength training (ST) with blood flow restriction (BFR) is known to promote increases in hypertrophy and strength sometimes similar to traditional ST despite the effects of the arterial BFR on muscle adaptations and safety are not well esta
Externí odkaz:
https://doaj.org/article/269e03ec1f6c4f82b0d111211dc094e4
Publikováno v:
European Journal of Clinical Pharmacology. 50:139-145
Objective: Tirilazad mesylate is a membrane lipid peroxidation inhibitor being evaluated for the treatment of patients with subarachnoid haemorrhage (SAH); phenobarbital may be administered to these patients for seizure prophylaxis. Therefore, the ef
Publikováno v:
Human Psychopharmacology: Clinical and Experimental. 10:97-104
The effect on digit-symbol substitution (DSST) of duration and extent of exposure to midazolam was studied in seven healthy male volunteers. Individual pharmacokinetic and pharmacodynamic parameters were estimated after a 7·5 mg intravenous bolus do
Publikováno v:
Clinical Pharmacology and Therapeutics. 56:389-397
The pharmacokinetic interaction between phenytoin and tirilazad was studied in 12 healthy men who received 200 mg phenytoin orally every 8 hours for 11 doses and 100 mg for the remaining 5 doses in one period of a two-way crossover study. In both per
Publikováno v:
The Journal of Clinical Pharmacology. 34:837-841
The potential interaction between tirilazad mesylate, a membrane lipid peroxidation inhibitor, and nimodipine, a calcium-channel antagonist, was assessed in 12 healthy male volunteers. Subjects received 60 mg nimodipine orally, 2.0 mg/kg tirilazad me
Autor:
John D Harry, Joseph C. Fleishaker, G.R. Peters, Penelope Ward, D Mark Wright, Laura K. Hulst
Publikováno v:
Clinical Pharmacology and Therapeutics. 55:378-384
Tirilazad mesylate pharmacokinetics were assessed in 12 young and 12 elderly volunteers (six men and six women per age group). Subjects received single 10-minute intravenous infusions of 1.5 mg/kg and 3.0 mg/kg tirilazad mesylate. Plasma tirilazad me
Publikováno v:
Pharmaceutical Research. 11:341-344
Publikováno v:
Journal of clinical pharmacology. 37(6)
Pramipexole is a dopamine receptor agonist that has proved effective in the treatment of Parkinson's disease. The pharmacokinetic properties of pramipexole at steady-state concentrations were studied in 16 healthy men and women at four dose levels th
Publikováno v:
European journal of clinical pharmacology. 50(4)
The pharmacokinetics of tirilazad mesylate and an active reduced metabolite, U89678, were studied in 7 volunteers with mild cirrhosis of the liver, and seven age, sex, weight and smoking status matched healthy normal volunteers. Subjects received a s
Publikováno v:
American journal of therapeutics. 2(8)
The pharmacokinetics of tirilazad were assessed in men ages 40--60 years, women