Frequency and impact of informant replacement in Alzheimer disease research.

about

Study partners perform essential tasks in dementia research and can experience burdens and benefits in this role.Consider the Source: The Implications of Informant Type on Outcome Assessments.Study partners: essential collaborators in discovering treatments for Alzheimer's disease

P2860

Q38834374-8F4D73B0-AEE6-4DCA-9AFB-77C6796ED110 Q43170003-23003453-B391-4939-B4D4-9D3036FBD354 Q59128442-7BC9A991-4F89-4E33-BD8D-C008B5DDFB15

P2860

Frequency and impact of informant replacement in Alzheimer disease research.

Item

http://www.wikidata.org/entity/Q35802122

description

2014 nî lūn-bûn

@nan

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

2014年论文

@zh

2014年论文

@zh-cn

name

Frequency and impact of informant replacement in Alzheimer disease research.

@ast

Frequency and impact of informant replacement in Alzheimer disease research.

@en

type

Item

label

Frequency and impact of informant replacement in Alzheimer disease research.

@ast

Frequency and impact of informant replacement in Alzheimer disease research.

@en

prefLabel

Frequency and impact of informant replacement in Alzheimer disease research.

@ast

Frequency and impact of informant replacement in Alzheimer disease research.

@en

P1476

Frequency and impact of informant replacement in Alzheimer disease research.

@en

P2093

David Elashoff

http://www.w3.org/2001/XMLSchema#string

Joshua D Grill

http://www.w3.org/2001/XMLSchema#string

Yan Zhou

http://www.w3.org/2001/XMLSchema#string

P2860

“Mini-mental state”

The Clinical Dementia Rating (CDR): current version and scoring rules

Modeling of Functional Assessment Questionnaire (FAQ) as continuous bounded data from the ADNI database.

The Uniform Data Set (UDS): clinical and cognitive variables and descriptive data from Alzheimer Disease Centers.

The National Alzheimer's Coordinating Center (NACC) database: the Uniform Data Set.

Neurobehavioral and neuropsychiatric symptoms in Alzheimer's disease: characteristics and treatment.

Issues affecting minority participation in research studies of Alzheimer disease.

An inventory to assess activities of daily living for clinical trials in Alzheimer's disease. The Alzheimer's Disease Cooperative Study.

Why are spousal caregivers more prevalent than nonspousal caregivers as study partners in AD dementia clinical trials?

Recruitment and retention of latino dementia family caregivers in intervention research: issues to face, lessons to learn.

P304

242-248

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1097/WAD.0000000000000078

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Jason Karlawish

P577

2014-12-30T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

25551863

http://www.w3.org/2001/XMLSchema#string

P921

Alzheimer's disease

P932

4486637

http://www.w3.org/2001/XMLSchema#string

Frequency and impact of informant replacement in Alzheimer disease research.

about

P2860

P2860

Frequency and impact of informant replacement in Alzheimer disease research.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932