Zobrazeno 1 - 10
of 16
pro vyhledávání: '"S. I. Gracon"'
Autor:
David S. Knopman, Fraser B. Smith, S. I. Gracon, S. Talwalker, T. M. Hoover, Lon S. Schneider, K. Davis
Publikováno v:
Neurology. 47:166-177
Objective: To assess the possible association between tacrine (Cognex, manufactured by Parke-Davis, Morris Plains, NJ) dose and likelihood of nursing home placement (NHP) or death in patients with AD. Design: A 30-week, randomized, double-blind, plac
Publikováno v:
Dementia and Geriatric Cognitive Disorders. 7:260-266
We studied the effects of 40 and 80 mg/day of tacrine on patients with probable Alzheimer''s disease (AD) in an 8-week, randomized, double-blind, placebo-controlled crossover trial with an enriched-population design. In the initial dose titration pha
Autor:
R. C. Petersen, C. R. Jack, Yuecheng Xu, P. C. O'Brien, S. I. Gracon, Ruth H. Cha, M. Slomkowski, Joel P. Felmlee, Maria Shiung, K. Stewart, T. M. Hoover, D. S. Knopman
To assess the feasibility of using MRI measurements as a surrogate endpoint for disease progression in a therapeutic trial for AD.A total of 362 patients with probable AD from 38 different centers participated in the MRI portion of a 52-week randomiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::409138d4f92d5a57b48ad7f475dd4e85
https://europepmc.org/articles/PMC2745302/
https://europepmc.org/articles/PMC2745302/
Publikováno v:
Dementia (Basel, Switzerland). 7(5)
We studied the effects of 40 and 80 mg/day of tacrine on patients with probable Alzheimer's disease (AD) in an 8-week, randomized, double-blind, placebo-controlled crossover trial with an enriched-population design. In the initial dose titration phas
Publikováno v:
JAMA. 271(13)
To evaluate the efficacy and safety of high-dose tacrine hydrochloride over 30 weeks in patients with probable Alzheimer's disease.A 30-week randomized, double-blind, placebo-controlled, parallel-group trial.Outpatients at 33 US centers.Men and women
Autor:
S. I. Gracon, David S. Knopman
Publikováno v:
Neurology. 44(2)
We examined the performance of patients with probable Alzheimer's disease (AD) who participated in the placebo arm of a 12-week clinical trial. Assessments occurred at baseline and at 4, 6, 10, and 12 weeks after starting study medication. Patients r
Publikováno v:
JAMA. 268(18)
To compare efficacy and safety of tacrine hydrochloride with placebo in patients with probable Alzheimer's disease.A 12-week, double-blind, placebo-controlled, parallel-group study.Outpatients at 23 centers.Men and women with probable Alzheimer's dis
Autor:
N R, Cutler, A J, Sedman, P, Prior, B A, Underwood, A, Selen, L, Balogh, A W, Kinkel, S I, Gracon, E R, Gamzu
Publikováno v:
Psychopharmacology bulletin. 26(2)
Neurochemical studies of Alzheimer's disease (AD) suggest deficiencies in the cholinergic system. We evaluated the steady-state pharmacokinetics of tacrine (Cognex), an oral cholinesterase inhibitor, in 12 patients with AD. Patients sequentially rece
Publikováno v:
Neurology. 49:898-899
Reply from the Authors: Thal and colleagues offer several criticisms involving methodological issues, including the obvious critique of observational cohort studies that the results are those of a "healthy patient" effect "since it is plausible, logi
Publikováno v:
The Lancet. 348:275-276