Klitzman, Robert
Robert Klitzman American psychiatrist and bioethicist
Klitzman, Robert, 1958-
Klitzman, Robert L. 1958-
Klitzman, Robert, (Robert L.), 1958-
Klitzman, Robert, College of Physicians and Surgeons
VIAF ID: 60622686 (Personal)
Permalink: http://viaf.org/viaf/60622686
Preferred Forms
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100 1 _ ‡a Klitzman, Robert
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100 1 _ ‡a Klitzman, Robert
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100 1 _ ‡a Klitzman, Robert
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100 1 _ ‡a Klitzman, Robert
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100 1 _ ‡a Klitzman, Robert L. ‡d 1958-
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100 1 _ ‡a Klitzman, Robert ‡d 1958-
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100 1 _ ‡a Klitzman, Robert, ‡d 1958-
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100 0 _ ‡a Robert Klitzman ‡c American psychiatrist and bioethicist
4xx's: Alternate Name Forms (13)
Works
Title | Sources |
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Am I my genes? : confronting fate and family secrets in the age of genetic testing |
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Being positive : the lives of men and women with HIV |
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Designing babies : how technology is changing the ways we create children |
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Doctor, will you pray for me? : medicine, chaplains, and healing the whole person |
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Double lives, 2007: |
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The ethics police? : the struggle to make human research safe |
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Furueru yama : Kūrū shokujin kyōgyūbyō |
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How good does the science have to be in proposals submitted to Institutional Review Boards? An interview study of Institutional Review Board personnel |
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How Infertility Patients and Providers View and Confront Religious and Spiritual Issues. |
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How local IRBs view central IRBs in the US |
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How old is too old? Challenges faced by clinicians concerning age cutoffs for patients undergoing in vitro fertilization |
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How Single Institutional Review Boards Manage Their Own Conflicts of Interest: Findings From a National Interview Study |
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How US institutional review boards decide when researchers need to translate studies |
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Hwanja ga doen uisadeul |
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Impact of patient education videos on genetic counseling outcomes after exome sequencing |
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Impact of Receiving Secondary Results from Genomic Research: A 12-Month Longitudinal Study. |
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The impact of social contexts in testing for alpha-1 antitrypsin deficiency: the roles of physicians and others |
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The importance of social, cultural, and economic contexts, and empirical research in examining "undue inducement". |
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In a house of dreams and glass, 1995: |
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Incubation period of human prion disease. |
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Intrinsic Healing of the Anterior Cruciate Ligament in an Adolescent. |
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Kamakahi vs ASRM and the future of compensation for human eggs |
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Kuru fieldwork in 1981 ... and beyond |
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Legal Immunity for Physicians During the Covid-19 Pandemic: Needs to Address Legal and Ethical Challenges |
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Linguistic and Cultural Challenges in Communication and Translation in US-Sponsored HIV Prevention Research in Emerging Economies |
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Local IRBs vs. federal agencies: shifting dynamics, systems, and relationships |
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Local Knowledge and Single IRBs for Multisite Studies: Challenges and Solutions |
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MDMA ('ecstasy') use, and its association with high risk behaviors, mental health, and other factors among gay/bisexual men in New York City |
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Mortal secrets : truth and lies in the age of AIDS |
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The Myth of Community Differences as the Cause of Variations Among IRBs |
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The Need for Vigilance in the Marketing of Genomic Tests in Psychiatry |
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Needs to Prepare for "Post-COVID-19 Syndrome" |
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New challenges for electronic health records: confidentiality and access to sensitive health information about parents and adolescents |
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Pain during embryo transfer is independently associated with clinical pregnancy in fresh/frozen assisted reproductive technology cycles |
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Patterns of Communication Between Gay and Lesbian Patients and Their Health Care Providers |
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Predictive testing and clinical trials in Huntington's disease: An ethical analysis |
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Presidents' Health and Medical Confidentiality |
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Presymptomatic Testing of Children for Huntington's Disease. |
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Problems in comprehension of informed consent in rural and peri-urban Mali, West Africa |
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The process of deciding about prophylactic surgery for breast and ovarian cancer: Patient questions, uncertainties, and communication |
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Psychiatrists' views of the genetic bases of mental disorders and behavioral traits and their use of genetic tests |
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Qualifying Confidentiality: Historical and Empirical Issues and Facts |
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Questions, Complexities, and Limitations in Disclosing Individual Genetic Results |
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Recruiting egg donors online: an analysis of in vitro fertilization clinic and agency websites' adherence to American Society for Reproductive Medicine guidelines |
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Reducing the number of fetuses in a pregnancy: providers' and patients' views of challenges |
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Reducing the Single IRB Burden: Streamlining Electronic IRB Systems |
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Reliance agreements and single IRB review of multisite research: Concerns of IRB members and staff |
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The reporting of monetary compensation in research articles |
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Research ethics. To protect human subjects, review what was done, not proposed |
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Research Participants' Preferences for Hypothetical Secondary Results from Genomic Research |
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Researchers' views on return of incidental genomic research results: qualitative and quantitative findings |
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Return of secondary genomic findings vs patient autonomy: implications for medical care |
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Reviewing HIV-Related Research in Emerging Economies: The Role of Government Reviewing Agencies |
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Roles of genetics and blood type in clinical responses to COVID-19: ethical and policy concerns |
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Seeing risk and reward through a patient's eyes |
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Should life insurers have access to genetic test results? |
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Single IRBs in Multisite Trials: Questions Posed by the New NIH Policy. |
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Struggles in Defining and Addressing Requests for "Family Balancing": Ethical Issues Faced by Providers and Patients. |
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Suture-button versus screw fixation of the syndesmosis: a biomechanical analysis. |
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Trembling mountain : a personal account of kuru, cannibals, and mad cow disease |
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Typologies of Altruistic and Financial Motivations for Research Participation |
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Unconventional combinations of prospective parents: ethical challenges faced by IVF providers |
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US IRBs confronting research in the developing world |
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The use of eggs and embryos in stem cell research |
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Views and experiences of IRBs concerning research integrity |
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Views of discrimination among individuals confronting genetic disease |
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Views of internists towards uses of PGD |
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Views of IRBs Concerning their Local Ecologies: Perceptions of Relationships, Systems, and Tensions between IRBs and their Institutions |
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Views of preimplantation genetic diagnosis among psychiatrists and neurologists |
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Views of the process and content of ethical reviews of HIV vaccine trials among members of US institutional review boards and South African research ethics committees |
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Voluntariness of consent to research: a preliminary empirical investigation. |
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When doctors become patients |
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When IRBs Say No to Participating in Research about Single IRBs |
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Whether to Waive Parental Permission in HIV Prevention Research Among Adolescents: Ethical and Legal Considerations |
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"Will they be good enough parents?": Ethical dilemmas, views, and decisions among assisted reproductive technology (ART) providers. |
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A year-long night, 1989: |
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환자가 된 의사들 고장난 신들의 생존에 관한 기록 |
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震える山 : クールー, 食人, 狂牛病 |
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