Literature DB >> 12208889

Cancer registries: should informed consent be required?

John Illman.   

Abstract

Entities:  

Mesh:

Year:  2002        PMID: 12208889     DOI: 10.1093/jnci/94.17.1269

Source DB:  PubMed          Journal:  J Natl Cancer Inst        ISSN: 0027-8874            Impact factor:   13.506


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  3 in total

Review 1.  Implications of data protection legislation for family history.

Authors:  Anneke Lucassen; Michael Parker; Robert Wheeler
Journal:  BMJ       Date:  2006-02-04

2.  Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons.

Authors:  Amy L McGuire; Mary A Majumder; Angela G Villanueva; Jessica Bardill; Juli M Bollinger; Eric Boerwinkle; Tania Bubela; Patricia A Deverka; Barbara J Evans; Nanibaa' A Garrison; David Glazer; Melissa M Goldstein; Henry T Greely; Scott D Kahn; Bartha M Knoppers; Barbara A Koenig; J Mark Lambright; John E Mattison; Christopher O'Donnell; Arti K Rai; Laura L Rodriguez; Tania Simoncelli; Sharon F Terry; Adrian M Thorogood; Michael S Watson; John T Wilbanks; Robert Cook-Deegan
Journal:  J Law Med Ethics       Date:  2019-03       Impact factor: 1.718

Review 3.  Developing National Cancer Registration in Developing Countries - Case Study of the Nigerian National System of Cancer Registries.

Authors:  Elima E Jedy-Agba; Emmanuel A Oga; Michael Odutola; Yusuf M Abdullahi; Abiodun Popoola; Peter Achara; Enoch Afolayan; Adekunbiola Aina Fehintola Banjo; Ima-Obong Ekanem; Olagoke Erinomo; Emmanuel Ezeome; Festus Igbinoba; Christopher Obiorah; Olufemi Ogunbiyi; Abidemi Omonisi; Clement Osime; Cornelius Ukah; Patience Osinubi; Ramatu Hassan; William Blattner; Patrick Dakum; Clement A Adebamowo
Journal:  Front Public Health       Date:  2015-07-30
  3 in total

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