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cholinesterase-inhibitors
17 studies tagged cholinesterase-inhibitors, dated 1998-05-01 to 2020-01-28. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- An update on the utility and safety of cholinesterase inhibitors for the treatment of Alzheimer's disease 2020-01-28
- Comparative safety and effectiveness of cholinesterase inhibitors and memantine for Alzheimer's disease: a network meta-analysis of 41 randomized controlled trials 2018-12-27
- Donepezil-based multi-functional cholinesterase inhibitors for treatment of Alzheimer's disease 2018-09-13
Studies
17 studies carry this tag.
Date range
1998 to 2020
Top journals
- The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry 2
- Alzheimer's research & therapy 1
- Archives of internal medicine 1
- Biological psychiatry 1
- Current medicinal chemistry 1
16 journals in all.
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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Alzheimer's disease (AD) is the most common cause of major neurocognitive disorders with a prevalence in the US of about 5.7 million in 2018.
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Pharmacological interventions have beneficial effects on cognition, function, and global changes, but not on neuropsychiatric symptoms, through current network meta-analysis.
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38/100
Alzheimer's disease (AD) is one of the most common neurodegenerative disorders in elderly people.
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Intervention- and patient-related factors modify the effect of cholinesterase inhibitors in patients with Alzheimer's disease.
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This survey analyzes two national pharmacovigilance databases in order to determine the major adverse reactions observed with the use of cholinesterase inhibitors in dementia.
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Cholinesterase inhibitor use was associated with a reduced risk of MI and death in a nationwide cohort of subjects diagnosed with Alzheimer's dementia.
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Alzheimer's disease (AD) is the most common cause of memory impairment and dementia in the elderly.
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Alzheimer's disease (AD) is a progressive neurodegenerative disorder of the central nervous system (CNS) which is the most common cause of dementia in the elderly.
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Use of cholinesterase inhibitors is associated with an increased risk of receiving an anticholinergic drug to manage urinary incontinence.
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Huperzine A (HupA), isolated from Chinese herb Huperzia serrata, is a potent, highly specific and reversible inhibitor of acetylcholinesterase.
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62/100
A systematic program of cognitive rehabilitation can result in maintained improvement in performance on specific cognitive and functional tasks in mildly impaired AD patients.
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Cholinesterase inhibitors (ChE-Is) are the standard of therapy for treatment of patients with Alzheimer disease (AD) and are the only class of drugs approved by the Food and Drug Administration (FDA) for treatment of this condition.
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Despite the proven efficacy of acetylcholinesterase inhibitors in Alzheimer's disease, there is a need for new and more effective treatments.
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Alzheimer's disease (AD) is the most common age-related neurodegenerative disease and has become an urgent public health problem in most areas of the world.
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This study was designed to compare the in vitro inhibitory effects on acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) of donepezil and some other cholinesterase (ChE) inhibitors which have been developed for the treatment of Alzheimer's disease.
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Potential therapeutic strategies for AD treatment include palliative treatment with nonspecific neuroprotecting agents, symptomatic treatment with psychotropic drugs for noncognitive symptoms, cognitive treatment with cognition enhancers, substitutive treatment with cholinergic enhancers to improve memory deficits, multifactorial treatment using several drugs in combination and etiopathogenic treatment designed to regulate molecular factors potentially associated with AD pathogenesis.
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This review starts with an historical background of the pharmacological development of tacrine almost fifty years ago (1949).