Zobrazeno 1 - 6
of 6
pro vyhledávání: '"M. W. Lunnon"'
Publikováno v:
Cerebrovascular Diseases. 8:31-37
Background: 619C89 is a use-dependent sodium channel blocker which reduces hemispheric infarction volume by up to 60% after permanent middle cerebral artery occlusion in rats. Intravenous doses of up to 1 mg/kg have been well tolerated by healthy you
Autor:
I. J. Fraser, Keith W. Muir, John Posner, M. W. Lunnon, S. F. Hobbiger, Z. Hussein, Kennedy R. Lees
Publikováno v:
British Journal of Clinical Pharmacology. 41:505-511
1. This was a multi-centre, placebo controlled, randomized, dose-escalating design study in which five dosing regimens of 619C89/placebo were evaluated in 48 stroke patients. Loading infusions of 0.5, 1, 1.5, 2 and 2.5 mg kg-1 over 1 h were followed
Autor:
M. W. Lunnon, D. W. Davies, H. P. Keller, J. Erwin, N. M. G. Debbas, G.S. Butrous, A. J. Camm, Anthony W. Nathan
Publikováno v:
European heart journal. 9(5)
DPI201-106 is a new positive inotropic agent. The cardiac electrophysiology of 16 patients was studied before and during DPI 201-106 administration (loading dose of intravenous DPI 201-106, 1.8 mg kg-1 h-1 administered over 10 min, followed by a main
Publikováno v:
Chemischer Informationsdienst. 9
Publikováno v:
European heart journal. 9(5)
DPI 201-106 is a novel compound unrelated to other cardioactive agents and has been shown to have an inotropic effect in animal preparations. The drug was given by intravenous infusion (20 mg over 10 min) to 10 patients with moderate cardiac failure
Autor:
M. W. LUNNON, J. MACMILLAN
Publikováno v:
Chemischer Informationsdienst. 9