Who Is Responsible for Promoting Equity in Rare Disease Research?

American Journal of Bioethics 23 (7):83-85 (2023)
  Copy   BIBTEX

Abstract

Stories of rare disease advocacy can elicit strong but ambivalent responses. It’s moving to read about the heroic efforts of parents “becoming drug developers to find a cure for their children’s ra...

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 92,497

External links

Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

Similar books and articles

Rare Disease, Advocacy, and Caregiver Burnout.Gretchen Agans - 2023 - American Journal of Bioethics 23 (7):91-94.
Reliance on Advocacy is the Symptom Not the Disease.Lynette Hammond Gerido - 2023 - American Journal of Bioethics 23 (7):86-88.
Rare Disease Research.Francesc Palau & Carmen Ayuso - 2023 - In Erick Valdés & Juan Alberto Lecaros (eds.), Handbook of Bioethical Decisions. Volume I: Decisions at the Bench. Springer Verlag. pp. 123-143.
Regulatory options for gender equity in health research.Belinda Bennett & Isabel Karpin - 2008 - International Journal of Feminist Approaches to Bioethics 1 (2):80-99.
Orphan Tests.Leslie G. Biesecker - 1996 - Cambridge Quarterly of Healthcare Ethics 5 (2):300.
Child Bereavement and Rare Diseases.Solange do Carmo Bowoniuk Wiegand & Caroline Filla Rosaneli - 2019 - Revista Iberoamericana de Bioética 10 (10):1-11.

Analytics

Added to PP
2023-06-22

Downloads
12 (#1,092,565)

6 months
7 (#441,920)

Historical graph of downloads
How can I increase my downloads?