These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 25756926)

  • 1. [Data linkage - respondents consent without selectivity?].
    Schröder H; Kleudgen M; Steinwede J; March S; Swart E; Stallmann C
    Gesundheitswesen; 2015 Apr; 77(4):e57-62. PubMed ID: 25756926
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Record linkage research and informed consent: who consents?
    Huang N; Shih SF; Chang HY; Chou YJ
    BMC Health Serv Res; 2007 Feb; 7():18. PubMed ID: 17291357
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [The Willingness to Consent to the Linkage of Primary and Secondary Data: An Analysis Based on a Survey of Patients with Primary Breast Cancer in Northrhine Westfalia].
    Scholten N; Pfaff H; Raabe N; Kowalski C
    Gesundheitswesen; 2017 Mar; 79(3):210-218. PubMed ID: 26619218
    [No Abstract]   [Full Text] [Related]  

  • 4. [Procedures according to data protection laws for coupling primary and secondary data in a cohort study: the lidA study].
    March S; Rauch A; Thomas D; Bender S; Swart E
    Gesundheitswesen; 2012 Dec; 74(12):e122-9. PubMed ID: 22297825
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Factors Influencing Consent for Electronic Data Linkage in Urban Latinos.
    Bakken S; Yoon S; Suero-Tejeda N
    Stud Health Technol Inform; 2015; 216():984. PubMed ID: 26262286
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linking primary study data with administrative and claims data in a German cohort study on work, age, health and work participation: is there a consent bias?
    Stallmann C; Swart E; Robra BP; March S
    Public Health; 2017 Sep; 150():9-16. PubMed ID: 28605640
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Linkage of secondary data with cancer registry data on the basis of encrypted personal identifiers - results from a pilot study in North Rhine-Westphalia].
    Kajüter H; Batzler WU; Krieg V; Heidinger O; Hense HW
    Gesundheitswesen; 2012 Aug; 74(8-9):e84-9. PubMed ID: 22836935
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Impact of variations in anonymous record linkage on weight distribution and classification.
    Nasseh D; Stausberg J
    Stud Health Technol Inform; 2013; 192():922. PubMed ID: 23920696
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Individual Data Linkage of Survey Data with Claims Data in Germany-An Overview Based on a Cohort Study.
    March S
    Int J Environ Res Public Health; 2017 Dec; 14(12):. PubMed ID: 29232834
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Consent to data linkage in a large online epidemiological survey of 18-23 year old Australian women in 2012-13.
    Graves A; McLaughlin D; Leung J; Powers J
    BMC Med Res Methodol; 2019 Dec; 19(1):235. PubMed ID: 31829134
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Health services research using linked records: who consents and what is the gain?
    Young AF; Dobson AJ; Byles JE
    Aust N Z J Public Health; 2001 Oct; 25(5):417-20. PubMed ID: 11688619
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A model for consent-based privilege management in personal electronic health records.
    Heinze O; Bergh B
    Stud Health Technol Inform; 2014; 205():413-7. PubMed ID: 25160217
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Large panel-survey data demonstrated country-level and ethnic minority variation in consent for health record linkage.
    Cruise SM; Patterson L; Cardwell CR; O'Reilly D
    J Clin Epidemiol; 2015 Jun; 68(6):684-92. PubMed ID: 25753658
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of four studies in a comparative framework reveals: health linkage consent rates on British cohort studies higher than on UK household panel surveys.
    Knies G; Burton J
    BMC Med Res Methodol; 2014 Nov; 14():125. PubMed ID: 25430545
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Consent and widespread access to personal health information for the delivery of care: a large scale telephone survey of consumers' attitudes using vignettes in New Zealand.
    Whiddett D; Hunter I; McDonald B; Norris T; Waldon J
    BMJ Open; 2016 Aug; 6(8):e011640. PubMed ID: 27554103
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The challenges of linking health insurer claims with electronic medical records.
    West SL; Johnson W; Visscher W; Kluckman M; Qin Y; Larsen A
    Health Informatics J; 2014 Mar; 20(1):22-34. PubMed ID: 24550563
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Young people's views about consenting to data linkage: findings from the PEARL qualitative study.
    Audrey S; Brown L; Campbell R; Boyd A; Macleod J
    BMC Med Res Methodol; 2016 Mar; 16():34. PubMed ID: 27001504
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Patient information, consents and privacy protection scheme for an information system dedicated to pervasive developmental disorders.
    Ben Said M; Robel L; Messiaen C; Craus Y; Jais JP; Golse B; Landais P
    Stud Health Technol Inform; 2014; 205():755-9. PubMed ID: 25160288
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Linking claims data and beneficiary survey information to report on the quality of health care: potential, pitfalls, and perspectives].
    Bitzer EM
    Gesundheitswesen; 2015 Feb; 77(2):e26-31. PubMed ID: 25622208
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Integration of primary and secondary data in the Study of Health in Pomerania and description of clinical outcomes using stroke as an example].
    Schmidt CO; Reber K; Baumeister SE; Schminke U; Völzke H; Chenot JF
    Gesundheitswesen; 2015 Feb; 77(2):e20-5. PubMed ID: 25714194
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.