All Stories

  1. Adolescent consent to treatment for gender dysphoria in England and Wales
  2. Human stem cell-based embryo models: innovation, ethics, and policy
  3. Last resort as a justification for compulsory nasogastric tube feeding of adults with anorexia nervosa
  4. What’s in a name? Abbasi and Another v Newcastle upon Tyne Hospitals NHS Foundation Trust ; Haastrup v King’s College Hospital NHS Foundation Trust [2025] UKS...
  5. Fifty years of the Congenital Disabilities (Civil Liability) Act 1976: A spent statute?
  6. Legal decisions on longstanding severe eating disorders
  7. Evolving judicial approaches to longstanding anorexia nervosa
  8. Afterword
  9. Advocating distinct regulatory paths for embryos and embryo-like structures
  10. How should we decide how to treat the child: harm versus best interests in cases of disagreement
  11. Book review: Medicine, Patients and the Law Medicine, Patients and the Law, BrazierMargaretCaveEmmaHeywoodRob, eds., 7th ed. (Manchester: Manchester University Press, 2023), 696 pp., 39.50 (GBP), ISBN 978 1 5261 5717 1
  12. The Warnock Report on Human Fertilisation and Embryology (1984)
  13. Skeleton Keys to Hospital Doors: Adolescent Adults who Refuse Life‐Sustaining Medical Treatment
  14. Should states restrict recipient choice amongst relevant and available COVID-19 vaccines?
  15. Involving parents in paediatric clinical ethics committee deliberations: a current controversy
  16. Clinical ethics support services during the COVID-19 pandemic in the UK: a cross-sectional survey
  17. Challenging misconceptions about clinical ethics support during COVID-19 and beyond: a legal update and future considerations
  18. Confirmation of the High Court’s Power to Override a Child’s Treatment Decision: A NHS Trust v X (In the matter of X (A Child) (No 2)) [2021] EWHC 65 (Fam)
  19. Valid consent to medical treatment
  20. Informing patients: The Bolam legacy
  21. COVID-19 Super-spreaders: Definitional Quandaries and Implications
  22. Selecting Treatment Options and Choosing Between them: Delineating Patient and Professional Autonomy in Shared Decision-Making
  23. Think of the Children: Liability for Non-Disclosure of Information Post-Montgomery
  24. EU Clinical Trials Regulation 2014: Fetter or facilitator?
  25. Who Knows Best (Interests)? The Case of Charlie Gard
  26. Editorial
  27. Debating the future of mandatory vaccination
  28. Mandated vaccination
  29. Montgomery, consent and the therapeutic exception
  30. Vulnerable patients
  31. Pioneering Healthcare Law
  32. Confidentiality
  33. Human rights, capacity and mental health
  34. Vaccination refusal
  35. Adolescent consent to medical treatment
  36. Competence and authority: adolescent treatment refusals for physical and mental health conditions
  37. Adolescent treatment refusal
  38. Fascilitating clinical research on vulnerable populations
  39. Adolescent Consent and Confi dentiality in the UK
  40. Why we wrote… Medicine, Patients and the Law
  41. Research ethics
  42. Reforming the ethical review system: balancing the rights and interests of research participants with the duty to facilitate good research
  43. Drink and Drugs in Pregnancy: Can the Law Prevent Avoidable Harm to the Future Child?
  44. Milgram and Tuskegee — Paradigm Research Projects in Bioethics
  45. New governance arrangements for research ethics committees: is facilitating research achieved at the cost of participants' interest
  46. Data protection legislation: interpretation and barriers to research
  47. Adolescent Consent to Medical Treatment