Joint replacement recipients' views about health information privacy. - Wikidata - wikimedia - TriplyDB

Joint replacement recipients' views about health information privacy.

Joint replacement recipients' views about health information privacy.

http://www.wikidata.org/entity/Q37333564

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Joint replacement recipients' views about health information privacy.

http://www.wikidata.org/entity/Q37333564

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article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

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scientific article published on October 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Joint replacement recipients' views about health information privacy.

@en

Joint replacement recipients' views about health information privacy.

@nl

type

label

Joint replacement recipients' views about health information privacy.

@en

Joint replacement recipients' views about health information privacy.

@nl

prefLabel

Joint replacement recipients' views about health information privacy.

@en

Joint replacement recipients' views about health information privacy.

@nl

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Health Expectations

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Joint replacement recipients' views about health information privacy.

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Amanda L Terry

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

Bert M Chesworth

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

Mark Speechley

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Paul Stolee

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Robert B Bourne

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

P2860

The gender gap: differences in political attitudes and social dominance orientation

Views on health information sharing and privacy from primary care practices using electronic medical records

Consent for use of personal information for health research: do people with potentially stigmatizing health conditions and the general public differ in their opinions?

What proportion of patients refuse consent to data collection from their records for research purposes?

Patients' consent preferences for research uses of information in electronic medical records: interview and survey data.

Learning from experience: privacy and the secondary use of data in health research.

Consent, confidentiality, and the Data Protection Act.

National survey of British public's views on use of identifiable medical data by the National Cancer Registry.

Variation in recruitment across sites in a consent-based clinical data registry: lessons from the Canadian Stroke Network

Community attitudes to the collection and use of identifiable data for health research--is it an invasion of privacy?

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1519-1529

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scholarly article

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10.1111/HEX.12142

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5

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18

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2013-10-01T00:00:00Z

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24112312

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