Filtros de búsqueda

Lista de obras de

A Web-Based Platform for Educating Researchers About Bioethics and Biobanking

artículo científico publicado en 2015

ASCO core values

artículo científico publicado en 2006

Academic oncology clinicians’ understanding of biosimilars and information needed before prescribing

Accelerating anticancer drug development - opportunities and trade-offs

scientific article published on 01 December 2018

Access to Children's Oncology Group and Pediatric Brain Tumor Consortium phase 1 clinical trials: Racial/ethnic dissimilarities in participation

artículo científico publicado en 2016

Allocating Scarce Healthcare Resources during Pandemics: Making the Case for Patients with Advanced and Metastatic Cancer

artículo científico publicado en 2020

Another look at the informed consent process: The document and the conversation

scientific article published on 27 October 2015

Balancing ethical goals in challenging individual participant scenarios occurring in a trial conducted with exception from informed consent

artículo científico publicado en 2015

Bioethical considerations of monoclonal B-cell lymphocytosis: donor transfer after haematopoietic stem cell transplantation

artículo científico publicado en 2007

Bioethics Training in Uganda: Report on Research and Clinical Ethics Workshops ⬇️

artículo científico publicado el 1 de marzo de 2011

Bioethics reformation style.

artículo científico publicado en 1994

Broad Consent for Research With Biological Samples: Workshop Conclusions

artículo científico publicado en 2015

Broad Consent for Research on Biospecimens: The Views of Actual Donors at Four U.S. Medical Centers

artículo científico publicado en 2018

Cancer Research Ethics and COVID-19

artículo científico publicado en 2020

Cancer donor preferences for disposition of their biospecimens after biobank closure.

artículo científico publicado en 2017

Caring for Colleagues and Loved Ones With Cancer

artículo científico publicado en 2018

Child and Parent Access to Transplant Information and Involvement in Treatment Decision Making

artículo científico publicado en 2018

Code status discussion: Just have one ⬇️

artículo científico publicado el 5 de abril de 2013

Communicating About Phase I Trials: Objective Disclosures Are Only A First Step ⬇️

artículo científico publicado el 4 de abril de 2012

Communication of randomization in childhood leukemia trials

artículo científico publicado en 2004

Community consultation for prehospital research: experiences of study coordinators and principal investigators

artículo científico publicado en 2014

Consulting communities when patients cannot consent: a multicenter study of community consultation for research in emergency settings

artículo científico publicado en 2014

Description of the types and content of phase 1 clinical trial consent conversations in practice

artículo científico publicado en 2015

Designing an ethical policy for bone marrow donation by minors and others lacking capacity

artículo científico publicado en 2004

Determinants of Patient and Surrogate Experiences With Acute Care Research Consent: A Key Informant Interview Study

scientific article published on 08 November 2019

Development and testing of a tool to assess patient preferences for phase I clinical trial participation

artículo científico publicado en 2014

Discussing molecular testing in oncology care: Comparing patient and physician information preferences

artículo científico publicado en 2017

Discussion of the do-not-resuscitate order: a pilot study of perceptions of patients with refractory cancer

artículo científico publicado en 2002

Does experience matter? Implications for community consultation for research in emergency settings

artículo científico publicado en 2017

Duty and altruism: alternative analyses of the ethics of sibling bone marrow donation

artículo científico publicado en 2006

Emergency Consent: Patients' and Surrogates' Perspectives on Consent for Clinical Trials in Acute Stroke and Myocardial Infarction

Emergency Research: Using Exception from Informed Consent, Evaluation of Community Consultations ⬇️

artículo científico publicado el 1 de enero de 2013

Enrolling subjects by exception from consent versus proxy consent in trauma care research

artículo científico publicado en 2007

Enrollment in research under exception from informed consent: the Patients' Experiences in Emergency Research (PEER) study

artículo científico publicado en 2013

Enrollment of Racial Minorities in Clinical Trials: Old Problem Assumes New Urgency in the Age of Immunotherapy

scientific article published on 01 January 2019

Ethical considerations of using a single minor donor for three bone marrow harvests for three HLA-matched siblings with primary immunodeficiency

artículo científico publicado en 2019

Ethical issues in identifying and recruiting participants for familial genetic research

artículo científico publicado en 2004

Ethics guidelines for research with the recently dead

artículo científico publicado en 2005

Ethics in Eye Banking: Understanding Professional Attitudes Toward Industry Changes

artículo científico publicado en 2020

Evaluation of a decision aid for families considering p53 genetic counseling and testing

artículo científico publicado en 2006

Family Strategies to Support Siblings of Pediatric Hematopoietic Stem Cell Transplant Patients

artículo científico publicado en 2017

From Protocols to Publications: A Study in Selective Reporting of Outcomes in Randomized Trials in Oncology

artículo científico publicado en 2015

HGG-09. DECISION MAKING IN THE FACE OF INCURABLE HIGH GRADE GLIOMAS: A QUALITATIVE ANALYSIS.

artículo científico publicado en 2018

Hereditary nonpolyposis colorectal cancer family members' perceptions about the duty to inform and health professionals' role in disseminating genetic information

artículo científico publicado en 2005

How does the collection of genetic test results affect research participants?

artículo científico publicado en 2007

Impact of individual clinical outcomes on trial participants' perspectives on enrollment in emergency research without consent

artículo científico publicado en 2016

Involving children with cancer in decision-making about research participation

artículo científico publicado en 2006

Issues, both ethical and practical, in the development and conduct of chemoprevention trials

artículo científico publicado en 2004

Learning from experience: a systematic review of community consultation acceptance data

artículo científico publicado en 2014

Partnering With Patients to Bridge Gaps in Consent for Acute Care Research

scientific article published on 01 June 2020

Patient and Surrogate Postenrollment Perspectives on Research Using the Exception From Informed Consent: An Integrated Survey

scientific article published on 20 May 2020

Patient and Surrogate Views of Community Consultation for Emergency Research

artículo científico publicado en 2017

Patient perspectives on compensation for biospecimen donation.

artículo científico publicado en 2018

Patient, caregiver and physician perspectives on participating in a thoracic rapid tissue donation program.

artículo científico publicado en 2017

Patients' perceptions of complementary and alternative medicine in head and neck cancer: a qualitative, pilot study with clinical implications

artículo científico publicado en 2013

Patients' perspectives of enrollment in research without consent: the patients' experiences in emergency research-progesterone for the treatment of traumatic brain injury study

artículo científico publicado en 2015

Phase I participants' views of quality of life and trial participation burdens

artículo científico publicado en 2007

Potential Benefits to Families, Children, and Adolescents Enrolled in Longitudinal Qualitative Research

artículo científico publicado en 2018

Provider Recommendations for Phase I Clinical Trials Within a Shared Decision-Making Model in Phase I Cancer Clinical Trial Discussions

scientific article published on 19 May 2020

Psychological functioning in persons considering genetic counseling and testing for Li-Fraumeni syndrome.

artículo científico publicado en 2008

Racial/ethnic diversity in children's oncology clinical trials: ten years later

artículo científico publicado en 2009

Real-world effectiveness of systemic agents approved for advanced non-small cell lung cancer: a SEER-Medicare analysis.

artículo científico publicado en 2013

Recommendations for the return of research results to study participants and guardians: a report from the Children's Oncology Group

artículo científico publicado en 2012

Referral Patterns and Clinical Outcomes for Transplant-Eligible Lymphoma and Myeloma Patients Evaluated at an Urban County Hospital

artículo científico publicado en 2016

Reframing Consent for Clinical Research: A Function-Based Approach

artículo científico publicado en 2017

Reply to Helping patients to understand terrifying news: Addressing the inner lives of physicians and extending beyond what we know

scientific article published on 19 February 2020

Research biopsies in phase I studies: views and perspectives of participants and investigators ⬇️

artículo científico publicado el 1 de marzo de 2012

Research on stored biological samples: views of African American and White American cancer patients

artículo científico publicado en 2006

Response to Open Peer Commentaries on "Partnering with Patients to Bridge Gaps in Consent for Acute Care Research"

scientific article published on 01 August 2020

Revisiting ethical guidelines for research with terminal wean and brain-dead participants.

artículo científico publicado en 2003

Shared decision-making in pediatric allogeneic blood and marrow transplantation: what if there is no decision to make?

artículo científico publicado en 2012

Smoking and Ethics: What Are the Duties of Oncologists? ⬇️

artículo científico publicado el 24 de agosto de 2010

Spreading it around: money for researcher and research participants.

artículo científico publicado en 2004

Stakeholder perceptions of thoracic rapid tissue donation: An exploratory study.

artículo científico publicado en 2013

Steps toward mapping the human vasculature by phage display.

artículo científico publicado en 2002

Study of the media's potential influence on prospective research participants' understanding of and motivations for participation in a high-profile phase I trial

artículo científico publicado en 2002

The Impact of Genetic Counseling Educational Tools on Patients' Knowledge of Molecular Testing Terminology

scientific article published on 07 May 2019

The ethical justification for minor sibling bone marrow donation: a case study

artículo científico publicado en 2008

The future of institutional review boards

artículo científico publicado en 2004

The newly and nearly dead

artículo científico publicado en 2003

The poster child for the need for central review of research protocols: the Children's Oncology Group.

artículo científico publicado en 2004

The vagaries of informed consent: experiences in oncologic care

artículo científico publicado el 1 de enero de 1995

Themes reported by families as important when proceeding with pediatric hematopoietic stem cell transplantation

artículo científico

Therapeutic misconception, misestimation, and optimism in participants enrolled in phase 1 trials.

artículo científico publicado en 2012

Unmet needs of siblings of pediatric stem cell transplant recipients

artículo científico publicado en 2014

Using Metaphors to Explain Molecular Testing to Cancer Patients

artículo científico publicado en 2017

Vascular ligand-receptor mapping by direct combinatorial selection in cancer patients

artículo científico publicado en 2011

Videos improve patient understanding of misunderstood chemotherapy terminology

scientific article published on 16 August 2019

Who should go first in trials with scarce agents? The views of potential participants

artículo científico publicado en 2007

Why many oncologists fail to share accurate prognoses: They care deeply for their patients

scientific article published on 27 November 2019

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda