Paul Stuart Appelbaum American psychiatrist
Appelbaum, Paul S.
Appelbaum, Paul S., 1951-
Appelbaum, P. S.
Appelbaum, Paul S., 19..-....
אפלבאום, פול ס.
VIAF ID: 22202541 (Personal)
Permalink: http://viaf.org/viaf/22202541
Preferred Forms
- 200 _ | ‡a Appelbaum ‡b Paul S.
- 100 1 _ ‡a Appelbaum, P. S.
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- 100 1 _ ‡a Appelbaum, Paul S
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- 100 1 _ ‡a Appelbaum, Paul S.
- 100 1 _ ‡a Appelbaum, Paul S.
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- 100 1 _ ‡a Appelbaum, Paul S. ‡d 1951-
- 100 1 _ ‡a Appelbaum, Paul S. ‡d 1951-
- 100 1 _ ‡a Appelbaum, Paul S., ‡d 19..-....
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- 100 0 _ ‡a Paul Stuart Appelbaum ‡c American psychiatrist
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4xx's: Alternate Name Forms (14)
5xx's: Related Names (1)
Works
Title | Sources |
---|---|
Almost a revolution mental health law and the limits of change | |
Assessing competence to consent to treatment : a guide for physicians and other health professionals | |
Clinical handbook of psychiatry and the law | |
The genetics of intelligence : ethics and the conduct of trustworthy research | |
Infōmudo konsento | |
Informed consent | |
Informing Social Security's process for financial capability determination | |
Kenkyu ni doisuru noryoku o sokuteisuru : Rinsho kenkyusha no tame no gaidorain. | |
Letter: Soviet Jewish physicians | |
Looking for the psychosocial impacts of genomic information | |
MacArthur competence assessment tool for treatment (MacCAT-T), 1998: | |
MacCAT-CR | |
n81119367 | |
Participants' Perceptions of Deep Brain Stimulation Research for Treatment-Resistant Depression: Risks, Benefits, and Therapeutic Misconception | |
Passive Monitoring of Mental Health Status in the Criminal Forensic Population | |
Patients' competence to consent to neurobiological research. | |
Patients' rights: the action moves to state courts. | |
Patterns of violent behavior among schizophrenic inpatients | |
Persistence and stability of delusions over time. | |
Personal Control Over Decisions to Participate in Research by Persons With Histories of Both Substance Use Disorders and Criminal Justice Supervision. | |
Physician-Assisted Death for Psychiatric Patients - Misguided Public Policy. | |
Placebo controls are not good science. | |
Policy statement on voting by persons with dementia residing in long-term care facilities | |
Preimplantation genetic diagnosis on in vitro fertilization clinic websites: presentations of risks, benefits and other information | |
Present at the creation: mental health law in eastern Europe and the former Soviet Union | |
Preservation of the capacity to appoint a proxy decision maker: implications for dementia research | |
Presidential Address: Re-Envisioning a Mental Health System for the United States | |
Prevalence and correlates of adequate performance on a measure of abilities related to decisional capacity: differences among three standards for the MacCAT-CR in patients with schizophrenia | |
Prevalence and phenomenology of violent ideation and behavior among 200 young people at clinical high-risk for psychosis: an emerging model of violence and psychotic illness | |
Privacy in psychiatric treatment: threats and responses | |
Privilege in the Federal Courts: should there be a "dangerous patient exception"? | |
Protecting privacy while facilitating research | |
Protecting staff from assaults by patients: OSHA steps in | |
Reducing therapeutic misconception: A randomized intervention trial in hypothetical clinical trials. | |
Reflections on the Goldwater Rule | |
Relationships between medicine and industry: approaches to the problem of conflicts of interest | |
Reliance agreements and single IRB review of multisite research: Concerns of IRB members and staff | |
The reporting of monetary compensation in research articles | |
Research ethics. To protect human subjects, review what was done, not proposed | |
Research Participants' Preferences for Hypothetical Secondary Results from Genomic Research | |
Researchers' access to patient records: an analysis of the ethical problems | |
Researchers' views on return of incidental genomic research results: qualitative and quantitative findings | |
Resource Document on Access to Firearms by People with Mental Disorders | |
Response to Faulkner et al | |
Response to the presidential address--the systematic defunding of psychiatric care: a crisis at our doorstep. | |
Responsibility for Suicide or Violence on Campus | |
Restoration of Firearm Rights in New York | |
Rethinking the conduct of psychiatric research | |
Return of secondary genomic findings vs patient autonomy: implications for medical care | |
Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network | |
The right to refuse treatment: the real issue is quality of care | |
The right to refuse treatment with antipsychotic medications: retrospect and prospect | |
Rights protection and advocacy: the need to do more with less. | |
The rising tide of patients' rights advocacy. | |
Risk-benefit decision making for treatment of depression during pregnancy | |
The role of the mental health professional in court | |
Sexual relationships between physicians and patients. | |
Should life insurers have access to genetic test results? | |
Should Mental Disorders Be a Basis for Physician-Assisted Death? | |
The silent majority: who speaks at IRB meetings? | |
Social media's challenges for psychiatry | |
Special section on APA's model commitment law: an introduction Key provision of APA's model law. | |
Standardizing return of participant results | |
Standards for civil commitment: a critical review of empirical research. | |
Starving in the midst of plenty: the mental health care crisis in America. | |
Statutes regulating patient-therapist sex. | |
The Subject Advocate: Protecting the Interests of Participants with Fluctuating Decisionmaking Capacity | |
Substance use, symptom, and employment outcomes of persons with a workplace mandate for chemical dependency treatment | |
Trauma and memory : clinical and legal controversies | |
Treatment-related decision-making capacity in middle-aged and older patients with psychosis: a preliminary study using the MacCAT-T and HCAT. | |
Unconscious conflict of interest: a Jewish perspective | |
Understanding Factors Associated with Uptake of BRCA1/2 Genetic Testing among Orthodox Jewish Women in the USA Using a Mixed-Methods Approach | |
Unrealistic optimism in early-phase oncology trials | |
Use of genetic tests among neurologists and psychiatrists: knowledge, attitudes, behaviors, and needs for training | |
Use of intervention strategies by assertive community treatment teams to promote patients' engagement. | |
Use of leverage over patients' money to promote adherence to psychiatric treatment | |
Violent Acts and Being the Target of Violence Among People With Mental Illness-The Data and Their Limits | |
Violent thoughts and violent behavior following hospitalization for mental disorder. | |
Voluntariness of consent to research: a conceptual model. | |
インフォームド・コンセント : 臨床の現場での法律と倫理 | |
研究に同意する能力を測定する : 臨床研究者のためのガイドライン |