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Brain Death Death

Analytical, Diagnostic and Therapeutic Techniques and Equipment29

Nontherapeutic Human Experimentation Human Experimentation Therapeutic Human Experimentation Patient Selection Clinical Trials as Topic Questionnaires Research Design Posthumous Conception Randomized Controlled Trials as Topic AIDS Serodiagnosis Prospective Studies Embryo Disposition Surgical Procedures, Operative Control Groups Medical Records Risk Assessment Surgical Procedures, Elective Records as Topic Pilot Projects Clinical Trials, Phase I as Topic Data Collection Cross-Sectional Studies Interviews as Topic Focus Groups Autopsy Resuscitation Stem Cell Research Feasibility Studies Treatment Outcome

Psychiatry and Psychology28

Mental Competency Disclosure Comprehension Personal Autonomy Refusal to Participate Confidentiality Paternalism Decision Making Researcher-Subject Relations Morals Truth Disclosure Treatment Refusal Physician-Patient Relations Duty to Warn Communication Attitude Parents Ethics Trust Attitude to Health Professional-Family Relations Family Health Knowledge, Attitudes, Practice Attitude of Health Personnel Focus Groups Altruism Dissent and Disputes Duty to Recontact

Disciplines and Occupations11

Nontherapeutic Human Experimentation Human Experimentation Therapeutic Human Experimentation Genetic Research Biomedical Research Research Design Emergency Medicine Research Stem Cell Research General Surgery Qualitative Research

Anthropology, Education, Sociology and Social Phenomena42

Informed Consent Consent Forms Presumed Consent Parental Consent Third-Party Consent Mental Competency Informed Consent By Minors Disclosure Personal Autonomy Confidentiality Child Advocacy Patient Rights Judicial Role Patient Advocacy Public Opinion Truth Disclosure Patient Education as Topic Privacy Treatment Refusal Duty to Warn Access to Information Government Regulation Jurisprudence Liability, Legal Malpractice Parents Family Human Rights Genetic Privacy Coercion Freedom Parental Notification Internationality Defensive Medicine Therapeutic Misconception Advance Directives Compensation and Redress Autopsy Organizational Policy Duty to Recontact Federal Government Human Body

Technology, Industry, Agriculture2

Multimedia Audiovisual Aids

Humanities24

Ethics, Research Personal Autonomy Ethics, Medical Ethics Committees, Research Beneficence Ethics, Clinical Bioethical Issues Morals Moral Obligations Ethics Committees Ethical Review Bioethics Helsinki Declaration Conflict of Interest Ethics Social Responsibility Ethics, Professional Codes of Ethics Principle-Based Ethics Therapeutic Misconception Empiricism Therapeutic Equipoise Philosophy, Medical Human Body

Information Science13

Disclosure Questionnaires Access to Information Communication Documentation Medical Records Multimedia Audiovisual Aids Records as Topic Information Dissemination Data Collection Interviews as Topic Focus Groups

Named Groups13

Minors Research Subjects Legal Guardians Mentally Ill Persons Persons Research Personnel Tissue Donors Parents Vulnerable Populations Proxy Patients Pregnant Women Nurse Anesthetists

Health Care76

Informed Consent Consent Forms Presumed Consent Parental Consent Third-Party Consent Mental Competency Informed Consent By Minors Ethics, Research Personal Autonomy Biological Specimen Banks Ethics, Medical Ethics Committees, Research Confidentiality Child Advocacy Patient Rights Ethics, Clinical Patient Advocacy Tissue and Organ Procurement Tissue Banks Patient Selection Patient Participation Patient Education as Topic Clinical Trials as Topic Privacy Questionnaires Treatment Refusal Physician-Patient Relations Ethics Committees Ethical Review Duty to Warn Bioethics Helsinki Declaration Government Regulation Selection Bias Professional Staff Committees Conflict of Interest Jurisprudence Liability, Legal Malpractice Ethics Patient Identification Systems Randomized Controlled Trials as Topic Attitude to Health Voluntary Programs Health Knowledge, Attitudes, Practice Human Rights Genetic Privacy Prospective Studies Ethics, Professional Freedom Medical Records Legislation, Medical Risk Assessment Patient Satisfaction Codes of Ethics Defensive Medicine Guidelines as Topic Records as Topic Pilot Projects Clinical Trials, Phase I as Topic Data Collection Patient Acceptance of Health Care Attitude of Health Personnel Cross-Sectional Studies Interviews as Topic Advance Directives Focus Groups Nurse Anesthetists Compensation and Redress Organizational Policy Duty to Recontact Feasibility Studies Federal Government Practice Guidelines as Topic Treatment Outcome Educational Status

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Diseases Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Technology, Industry, Agriculture Humanities Information Science Named Groups Health Care Geographicals

Informed Consent Consent Forms Presumed Consent Parental Consent Third-Party Consent Mental Competency Minors Research Subjects Informed Consent By Minors Nontherapeutic Human Experimentation Human Experimentation Ethics, Research Disclosure Comprehension Personal Autonomy Biological Specimen Banks Therapeutic Human Experimentation Ethics, Medical Ethics Committees, Research Refusal to Participate Confidentiality Genetic Research Child Advocacy Patient Rights Beneficence Biomedical Research Judicial Role Paternalism Legal Guardians Ethics, Clinical Patient Advocacy Tissue and Organ Procurement Tissue Banks Decision Making Patient Selection Public Opinion Patient Participation Researcher-Subject Relations Bioethical Issues Morals Truth Disclosure Patient Education as Topic Moral Obligations Clinical Trials as Topic Privacy Questionnaires Treatment Refusal Research Design Physician-Patient Relations Mentally Ill Persons Ethics Committees Ethical Review Great Britain Duty to Warn Persons Bioethics Helsinki Declaration Access to Information Government Regulation Selection Bias Professional Staff Committees Conflict of Interest Jurisprudence Research Personnel Tissue Donors Communication Liability, Legal Attitude Malpractice Posthumous Conception Parents Vulnerable Populations Ethics Emergency Medicine Patient Identification Systems Trust Documentation United States Randomized Controlled Trials as Topic Attitude to Health Social Responsibility Voluntary Programs Professional-Family Relations Family Proxy Health Knowledge, Attitudes, Practice Human Rights AIDS Serodiagnosis Genetic Privacy Prospective Studies Brain Death Ethics, Professional Research Coercion Embryo Disposition Surgical Procedures, Operative Freedom Control Groups Patients Medical Records

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