about
Regulation of research on the decisionally impaired: history and gaps in the current regulatory system.The National Bioethics Advisory Commission: bridging the gaps in human subjects research protection.Comments on the Second Report of the Maryland Attorney General's Research Working Group.Data-sharing and data-withholding in genetics and the life sciences: results of a national survey of technology transfer officers.Protecting vulnerable research subjects: practical realities of institutional review board review and approval.Bioethical malpractice: risk and responsibilities in human research.Research involving children: regulations, review boards and reform.DO ETHICS DEMAND EVALUATION OF PUBLIC HEALTH LAWS? SHIFTING SCIENTIFIC SANDS AND THE CASE OF YOUTH SPORTS-RELATED TRAUMATIC BRAIN INJURY LAWS.Managing conflict in an urban health care setting: what do "experts" know?Common ground: exploring policy approaches to addressing racial disparities from the left and the right.Discrimination based on HIV/AIDS and other health conditions: "disability" as defined under federal and state law.Bragdon v. Abbott: extending the Americans with Disability Act to asymptomatic individuals.Human experimentation in developing countries: improving international practices by identifying vulnerable populations and allocating fair benefits.Old legacies and new paradigms: confusing "research" and "treatment" and its consequences in responding to emergent health threats.The lead-based paint abatement repair and maintenance study in Baltimore: historic framework and study design.Conflict in health care organizations.Autonomy suspended: using female patients to teach intimate exams without their knowledge or consent.Pelvic examinations under anesthesia: an important teaching tool.Adverse impact of predisposition testing on major life activities: lessons from BRCA1/2 testing.Reproductive genetics 1991-2002: a selected annotated legal bibliography of genetic testing, gene transfer and reproductive cloning.Achieving proper balance in research with decisionally-incapacitated subjects: NAMI's perspectives on the working group's proposal.Regulating research with vulnerable populations: litigation gone awry.Proxy consent to participation of the decisionally impaired in medical resesarch--Maryland's policy initiative.Assessment of capacity to give consent to research participation: state-of-the-art and beyond.In harm's way: research subjects who are decisionally impaired.Issues raised by research using persons suffering from dementia who have impaired decisional capacity.Medicate-to-execute: current trends in death penalty jurisprudence and the perils of dual loyalty.Teaching without harming the living: performing minimally invasive procedures on the newly dead.AIDS and adolescents.Biotechnology and human dignity, a necessary and compatible union.The Kennedy Krieger case: judicial anger and the research enterprise.(Women and) children first: applicable to lifeboats? Applicable to human experimentation?Regulation of research with children: the evolution from exclusion to inclusion.Mediating disputes in managed care: resolving conflicts over covered services.Is there a pink slip in my gene? Genetic discrimination in the workplace.Ethical issues in conducting behavioral genetics research: the case of smoking prevention trials among adolescents.The argument against a physician's duty to warn for genetic diseases: the conflicts created by Safer v. Estate of Pack.What should the law say about disclosure of genetic information to relatives?Parental consent for children's participation in biomedical research: the ethical, regulatory, and judicial framework of Grimes v. Kennedy Krieger Institute, IncEuthanasia: a historical overview
P1433
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P1433
description
journal
@en
مجلة
@ar
name
Journal of Health Care Law and Policy
@en
type
label
Journal of Health Care Law and Policy
@en
prefLabel
Journal of Health Care Law and Policy
@en
P1055
P1058
P1476
Journal of Health Care Law and Policy
@en