Research article summary (published 11 Jun 2006):

What do people at risk for Alzheimer disease think about surrogate consent for research?

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Author information

Author/s: Schenk, Dale B (DB); Gilman, Sid (S);

Journal and publication information

Publication Type: Comment; Letter

Journal: Neurology (Neurology), published in United States. (Language: eng)

Reference: 2006-Jun; vol 66 (issue 11) : pp 1785-6

Dates: Created 2006/06/13; Completed 2006/07/05; Revised 2007/11/15;

PMID: 16769971, status: MEDLINE (last retrieval date: 12/26/2008)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

Comments and Corrections

CommentOn: Neurology. 2005 Nov 8;65(9):1395-401. (PMID: 16275826)

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Aged Aged, 80 and over Alzheimer Disease - physiopathology; prevention & control; therapy Attitude Caregivers - ethics; standards Clinical Protocols - standards Clinical Trials as Topic - ethics; standards Decision Making Female Humans

Humans Informed Consent - standards Male Mental Competency - standards Patient Selection - ethics Personal Autonomy Questionnaires Risk Factors Therapeutic Human Experimentation - ethics Third-Party Consent - ethics

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