Items where Author is "Mason, S."
Number of items: 10.
Public
ALLMARK, P. J. and MASON, S.
(2005).
Should desperate volunteers be included in randomised controlled trials?
Journal of Medical Ethics, 32 (9), 548-553.
[Article]
ALLMARK, P. J. and MASON, S.
(2005).
Improving the quality of consent to randomised controlled trials by using continuous consent and clinician training in the consent process.
Journal of Medical Ethics, 32 (8), p. 439.
[Article]
ALLMARK, P. J., MASON, S., GILL, A. B. and MEGONE, C.
(2003).
Obtaining consent for neonatal research.
Archives of disease in childhood: fetal and neonatal edition, 88 (3), F166-F167.
[Article]
None
ALLMARK, P. J., MASON, S. and MEGONE, C.
(2001).
Ethical issues and practical problems in obtaining informed consent for neonatal research.
In: MASON, S. and MEGONE, C., (eds.)
European neonatal research: consent, ethics committees and law.
Aldershot, Ashgate, 3-12.
[Book Section]
ALLMARK, P. J., MASON, S., GILL, A. B. and MEGONE, C.
(2001).
Is it in a neonate's best interest to enter a randomised controlled trial?
Journal of medical ethics, 27 (2), 110-113.
[Article]
DALLA-VORGIA, P., MASON, S., MEGONE, C., ALLMARK, P. J., BRATLID, D., GILL, A. B., MORROGH, P., PLOMER, A. and REITER-THEIL, S.
(2001).
Overview of European legislation on informed consent for neonatal research.
Archives of disease in childhood: fetal and neonatal edition, 84 (1), F70-F73.
[Article]
MEGONE, C., MASON, S. and ALLMARK, P. J.
(2001).
The attitudes of RECs in 11 European countries to informed consent in neonatal research.
In: MASON, S. and MEGONE, C., (eds.)
European neonatal research: consent, ethics committees and law.
Aldershot, Ashgate, 43-62.
[Book Section]
MEGONE, C., MASON, S. and ALLMARK, P. J.
(2001).
The structure, composition and operation of European RECs.
In: MASON, S. and MEGONE, C., (eds.)
European neonatal research: consent, ethics committees and law.
Aldershot, Ashgate, 23-42.
[Book Section]
MEGONE, C., MASON, S. and ALLMARK, P. J.
(2001).
The views of RECs in eight European countries on the process of obtaining informed consent in neonatal research and on the structure and organisation of RECs.
In: MASON, S. and MEGONE, C., (eds.)
European neonatal research: consent, ethics committees and law.
Aldershot, Ashgate, 63-82.
[Book Section]
MASON, S. and ALLMARK, P. J.
(2000).
Obtaining informed consent to neonatal randomised controlled trials: interviews with parents and clinicians in the Euricon study.
The Lancet, 356 (9247), 2045-2051.
[Article]