Lista de obras - Gail Geller - Dominio Público Uruguay

"Am I cut out for this?" Understanding the experience of doubt among first-year medical students

artículo científico publicado en 2014

"My son is still walking": stages of receptivity to discussions of advance care planning among parents of sons with Duchenne muscular dystrophy

artículo científico publicado en 2006

'Someone should oversee it': patient perspectives on the ethical issues arising with the regulation of probiotics

artículo científico publicado en 2012

A "holistic" model of the healing relationship: what would that require of physicians?

artículo científico publicado en 2006

A Direct Observation Checklist to Measure Respect and Dignity in the ICU.

artículo científico publicado en 2016

Addressing Medical Students' Negative Bias Toward Patients With Obesity Through Ethics Education

article

Adolescent and parent perceptions on youth participation in risk behavior research

artículo científico publicado en 2006

Are practicing and future physicians prepared to obtain informed consent? The case of genetic testing for susceptibility to breast cancer

artículo científico publicado en 1998

Beyond "compliance": the role of institutional culture in promoting research integrity

artículo científico publicado en 2010

Communication predictors and consequences of Complementary and Alternative Medicine (CAM) discussions in oncology visits

artículo científico publicado en 2016

Complementary medicine and genetic medicine: polar disciplines or dynamic partners?

artículo científico publicado en 2005

Conflicts in Learning to Care for Critically Ill Newborns: "It Makes Me Question My Own Morals".

artículo científico publicado en 2015

Distress and burnout among genetic service providers

artículo científico publicado en 2009

Ethical Discourse about the Modification of Food for Therapeutic Purposes: How Patients with Gastrointestinal Diseases View the Good, the Bad, and the Healthy

artículo científico publicado en 2012

Ethical and practical issues associated with aggregating databases

artículo científico publicado en 2008

Ethical challenges in the care of children and families affected by life-limiting neuromuscular diseases

artículo científico publicado en 2012

Ethical considerations in global HIV phylogenetic research

article

Ethical issues in conducting behavioral genetics research: the case of smoking prevention trials among adolescents.

artículo científico publicado en 2002

Experiences of patients with chronic gastrointestinal conditions: in their own words

artículo científico publicado en 2012

Genomics and infectious disease: a call to identify the ethical, legal and social implications for public health and clinical practice

artículo científico publicado en 2014

Health care professionals' perceptions and experiences of respect and dignity in the intensive care unit

artículo científico publicado en 2015

Houseofficers' reactions to media coverage about the sequencing of the human genome

artículo científico publicado en 2003

How patients view probiotics: findings from a multicenter study of patients with inflammatory bowel disease and irritable bowel syndrome

artículo científico publicado en 2012

ICU-RESPECT: An index to assess patient and family experiences of respect in the intensive care unit

artículo científico publicado en 2016

Implications of the human genome initiative for the primary care physician

artículo científico publicado en 1991

Improving Clinician Attitudes of Respect and Trust for Persons With Sickle Cell Disease

artículo científico publicado en 2015

Informed consent for enrolling minors in genetic susceptibility research: a qualitative study of at-risk children's and parents' views about children's role in decision-making

artículo científico publicado en 2003

Institutional Responsibility and the Flawed Genomic Biomarkers at Duke University: A Missed Opportunity for Transparency and Accountability

artículo científico publicado en 2016

Listening in on difficult conversations: an observational, multi-center investigation of real-time conversations in medical oncology

artículo científico publicado en 2013

Looking Back, Looking Forward: The Ethical Framing of Complementary and Alternative Medicine in Oncology Over the Last 20 Years

artículo científico publicado en 2018

Mapping the human genome: an assessment of media coverage and public reaction

artículo científico publicado en 2002

Measuring patient respect in the intensive care unit: Validation of the ICU-RESPECT instrument.

artículo científico publicado en 2018

Observations of respect and dignity in the intensive care unit

artículo científico publicado en 2015

Opinions about new reproductive genetic technologies: hopes and fears for our genetic future

artículo científico publicado en 2005

Parents' and children's attitudes toward the enrollment of minors in genetic susceptibility research: implications for informed consent

artículo científico publicado en 2003

Patient and family perspectives on respect and dignity in the intensive care unit

artículo científico publicado en 2015

Perspectives on obesity and its treatment: health care providers and the general public in rural West Virginia and urban Baltimore

artículo científico publicado en 2013

Physicians' propensity to offer genetic testing for Alzheimer's disease: results from a survey

artículo científico publicado en 2002

Public expectations for return of results from large-cohort genetic research

artículo científico publicado en 2008

Public perspectives on informed consent for biobanking

Relationships hold the key to trustworthy and productive translational science: recommendations for expanding community engagement in biomedical research

artículo científico publicado en 2013

Relevant content for a patient-reported outcomes questionnaire for use in oncology clinical practice: Putting doctors and patients on the same page

artículo científico publicado en 2010

Roundtable: the politics of genetic testing

artículo científico publicado en 1996

Science communication reconsidered

article

Scientists' and science writers' experiences reporting genetic discoveries: toward an ethic of trust in science journalism

artículo científico publicado en 2005

The Practice of Respect in the Intensive Care Unit

artículo científico publicado en 2018

The essential role of medical ethics education in achieving professionalism: the Romanell Report

artículo científico publicado en 2015

The moral nature of patient-centeredness: is it "just the right thing to do"?

artículo científico publicado en 2005

The role and impact of personal faith and religion among genetic service providers

artículo científico publicado en 2009

Tolerance for ambiguity: an ethics-based criterion for medical student selection

artículo científico publicado en 2013

Toward a model informed consent process for BRCA1 testing: a qualitative assessment of women's attitudes

artículo científico publicado en 1997

Toward an optimal healing environment in pediatric rehabilitation.

artículo científico publicado en 2004

Transforming the culture of biomedical research from compliance to trustworthiness: insights from nonmedical sectors

artículo científico publicado en 2009

Transitioning to breast cancer survivorship: perspectives of patients, cancer specialists, and primary care providers

artículo científico publicado en 2009

Trustworthy Research Institutions: The Challenging Case of Studying the Genetics of Intelligence

artículo científico publicado en 2015

Understanding treatment with respect and dignity in the intensive care unit

artículo científico publicado en 2015

Use of Placebo in Supplementation Studies-Vitamin D Research Illustrates an Ethical Quandary.

artículo científico publicado en 2018

Viewpoint: the importance of worldviews for medical education.

artículo científico publicado en 2007

Was a decision made? An assessment of patient-clinician discordance in medical oncology encounters

artículo científico publicado en 2015

Weight-based stigma and physician bias

artículo científico publicado en 2010

What do clinicians derive from partnering with their patients? A reliable and valid measure of "personal meaning in patient care"

scientific article published on 15 May 2008

What does 'respect' mean? Exploring the moral obligation of health professionals to respect patients

artículo científico publicado en 2007

What keeps you up at night? Genetics professionals' distressing experiences in patient care

artículo científico publicado en 2010

What patients with addiction disorders need from their primary care physicians: A qualitative study

artículo científico publicado en 2015

Lista de obras de Gail Geller

"Am I cut out for this?" Understanding the experience of doubt among first-year medical students

"My son is still walking": stages of receptivity to discussions of advance care planning among parents of sons with Duchenne muscular dystrophy

'Someone should oversee it': patient perspectives on the ethical issues arising with the regulation of probiotics

A "holistic" model of the healing relationship: what would that require of physicians?

A Direct Observation Checklist to Measure Respect and Dignity in the ICU.

Addressing Medical Students' Negative Bias Toward Patients With Obesity Through Ethics Education

Adolescent and parent perceptions on youth participation in risk behavior research

Are practicing and future physicians prepared to obtain informed consent? The case of genetic testing for susceptibility to breast cancer

Beyond "compliance": the role of institutional culture in promoting research integrity

Communication predictors and consequences of Complementary and Alternative Medicine (CAM) discussions in oncology visits

Complementary medicine and genetic medicine: polar disciplines or dynamic partners?

Conflicts in Learning to Care for Critically Ill Newborns: "It Makes Me Question My Own Morals".

Distress and burnout among genetic service providers

Ethical Discourse about the Modification of Food for Therapeutic Purposes: How Patients with Gastrointestinal Diseases View the Good, the Bad, and the Healthy

Ethical and practical issues associated with aggregating databases

Ethical challenges in the care of children and families affected by life-limiting neuromuscular diseases

Ethical considerations in global HIV phylogenetic research

Ethical issues in conducting behavioral genetics research: the case of smoking prevention trials among adolescents.

Experiences of patients with chronic gastrointestinal conditions: in their own words

Genomics and infectious disease: a call to identify the ethical, legal and social implications for public health and clinical practice

Health care professionals' perceptions and experiences of respect and dignity in the intensive care unit

Houseofficers' reactions to media coverage about the sequencing of the human genome

How patients view probiotics: findings from a multicenter study of patients with inflammatory bowel disease and irritable bowel syndrome

ICU-RESPECT: An index to assess patient and family experiences of respect in the intensive care unit

Implications of the human genome initiative for the primary care physician

Improving Clinician Attitudes of Respect and Trust for Persons With Sickle Cell Disease

Informed consent for enrolling minors in genetic susceptibility research: a qualitative study of at-risk children's and parents' views about children's role in decision-making

Institutional Responsibility and the Flawed Genomic Biomarkers at Duke University: A Missed Opportunity for Transparency and Accountability

Listening in on difficult conversations: an observational, multi-center investigation of real-time conversations in medical oncology

Looking Back, Looking Forward: The Ethical Framing of Complementary and Alternative Medicine in Oncology Over the Last 20 Years

Mapping the human genome: an assessment of media coverage and public reaction

Measuring patient respect in the intensive care unit: Validation of the ICU-RESPECT instrument.

Observations of respect and dignity in the intensive care unit

Opinions about new reproductive genetic technologies: hopes and fears for our genetic future

Parents' and children's attitudes toward the enrollment of minors in genetic susceptibility research: implications for informed consent

Patient and family perspectives on respect and dignity in the intensive care unit

Perspectives on obesity and its treatment: health care providers and the general public in rural West Virginia and urban Baltimore

Physicians' propensity to offer genetic testing for Alzheimer's disease: results from a survey

Public expectations for return of results from large-cohort genetic research

Public perspectives on informed consent for biobanking

Relationships hold the key to trustworthy and productive translational science: recommendations for expanding community engagement in biomedical research

Relevant content for a patient-reported outcomes questionnaire for use in oncology clinical practice: Putting doctors and patients on the same page

Roundtable: the politics of genetic testing

Science communication reconsidered

Scientists' and science writers' experiences reporting genetic discoveries: toward an ethic of trust in science journalism

The Practice of Respect in the Intensive Care Unit

The essential role of medical ethics education in achieving professionalism: the Romanell Report

The moral nature of patient-centeredness: is it "just the right thing to do"?

The role and impact of personal faith and religion among genetic service providers

Tolerance for ambiguity: an ethics-based criterion for medical student selection

Toward a model informed consent process for BRCA1 testing: a qualitative assessment of women's attitudes

Toward an optimal healing environment in pediatric rehabilitation.

Transforming the culture of biomedical research from compliance to trustworthiness: insights from nonmedical sectors

Transitioning to breast cancer survivorship: perspectives of patients, cancer specialists, and primary care providers

Trustworthy Research Institutions: The Challenging Case of Studying the Genetics of Intelligence

Understanding treatment with respect and dignity in the intensive care unit

Use of Placebo in Supplementation Studies-Vitamin D Research Illustrates an Ethical Quandary.

Viewpoint: the importance of worldviews for medical education.

Was a decision made? An assessment of patient-clinician discordance in medical oncology encounters

Weight-based stigma and physician bias

What do clinicians derive from partnering with their patients? A reliable and valid measure of "personal meaning in patient care"

What does 'respect' mean? Exploring the moral obligation of health professionals to respect patients

What keeps you up at night? Genetics professionals' distressing experiences in patient care

What patients with addiction disorders need from their primary care physicians: A qualitative study