Similar articles

• Cohort profile: updating the cohort profile for the MRC National Survey of Health and Development: a new clinic-based data collection for ageing research.

  Kuh D, Pierce M, Adams J, Deanfield J, Ekelund U, Friberg P, Ghosh AK, Harwood N, Hughes A, Macfarlane PW, Mishra G, Pellerin D, Wong A, Stephen AM, Richards M, Hardy R; NSHD scientific and data collection team. Kuh D, et al. Int J Epidemiol. 2011 Feb;40(1):e1-9. doi: 10.1093/ije/dyq231. Int J Epidemiol. 2011. PMID: 21345808 Free PMC article. No abstract available.
• United Kingdom Primary Sjogren's Syndrome Registry--a united effort to tackle an orphan rheumatic disease.

  Ng WF, Bowman SJ, Griffiths B; UKPSSR study group. Ng WF, et al. Rheumatology (Oxford). 2011 Jan;50(1):32-9. doi: 10.1093/rheumatology/keq240. Epub 2010 Aug 6. Rheumatology (Oxford). 2011. PMID: 20693261 Review.
• Data security is crucial for Japanese science.

  Tsuboi E, Kawahara N, Mitsuishi T, Oshima A, Yonemoto S. Tsuboi E, et al. Nature. 2002 Jun 13;417(6890):689. doi: 10.1038/417689a. Nature. 2002. PMID: 12066154 No abstract available.
• Ethical and social aspects of genetics and neuroscience: the Wellcome proposals.

  Alderson P. Alderson P. Bull Med Ethics. 1998 Mar;No. 136:20-1. Bull Med Ethics. 1998. PMID: 11657530 No abstract available.
• Molecular genetic research on IQ: can it be done? Should it be done?

  Daniels J, McGuffin P, Owen M. Daniels J, et al. J Biosoc Sci. 1996 Oct;28(4):491-507. doi: 10.1017/s0021932000022550. J Biosoc Sci. 1996. PMID: 8973006 Review. No abstract available.