Darren Shickle

TL;DR: If primary care is to become more involved in the delivery of genetic services in the future, then a major educational effort is required to raise awareness of the potential scope and limitations of new developments.

TL;DR: The nature of the race controversy in the context of biomedical research is reviewed and several challenges to policy action are highlighted, including restrictions resulting from commercial or regulatory considerations, the difficulty in presenting precise terminology in the media, and drifting or ambiguous definitions of key terms.

TL;DR: The philosophy of the right to know and the right not to know, individual rights and genetics - the historical perspective - a comment on Ruth Chadwick's paper, Urban Wiesing sociological perspectives on the right-to-know, Mairi Levitt the meaning of "rights" in the right -to-not-know debate, Ingmar Lustgård as discussed by the authors, is there a need for a genetic privacy law?

TL;DR: A model was constructed and a checklist drawn up that contained the following elements: identifying issues, needs and partners; producing a strategy; securing funding; implementing changes; and monitoring and evaluating a telehealth project.

TL;DR: The large prevalence of sight loss and blindness in the UK population imposes significant costs on public funds, private expenditure, and health, highlighting the need for population-based studies that track the prevalence of Sight-impairing eye conditions and treatment effects over time.