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A Largent

Showing results (21-30 of 178) with videos related to

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The Hastings Center Report|May 24, 2012
Which orphans will find a home? The rule of rescue in resource allocation for rare diseasesEmily A Largent, Steven D Pearson
Journal of Medical Ethics|October 14, 2020
Compensating for research risk: permissible but not obligatoryHolly Fernandez Lynch, Emily A Largent
JAMA Neurology|February 19, 2024
Diagnosing Preclinical and Prodromal Neurodegenerative Diseases-The Clinical Is PoliticalClaire M Erickson, Emily A Largent
Clinical Trials (London, England)|December 21, 2018
Making the case for completion bonuses in clinical trialsEmily A Largent, Holly Fernandez Lynch
JAMA Neurology|January 4, 2022
Bringing Alzheimer Disease Testing and Results Disclosure Into the 21st Century Cures ActEmily A Largent, Angela R Bradbury
Perspectives in Biology and Medicine|November 29, 2021
The Legality and Ethics of Mandating COVID-19 VaccinationEmily A Largent, Franklin G Miller
Yale Journal of Health Policy, Law, and Ethics|December 19, 2017
Paying Research Participants: Regulatory Uncertainty, Conceptual Confusion, and a Path ForwardEmily A Largent, Holly Fernandez Lynch
The Journal of Infectious Diseases|May 30, 2020
Paying Participants in COVID-19 TrialsEmily A Largent, Holly Fernandez Lynch
BMJ (Clinical Research Ed.)|June 8, 2023
Considering tomorrow's patients in today's drug approvalsHolly Fernandez Lynch, Emily A Largent
The Hastings Center Report|April 11, 2021
Public Attitudes toward Consent When Research Is Integrated into Care-Any "Ought" from All the "Is"?Stephanie R Morain, Emily A Largent
Pageof 18

Showing results (21-30 of 178) with videos related to

Sort By:
Pageof 18
The Hastings Center Report|May 24, 2012
Which orphans will find a home? The rule of rescue in resource allocation for rare diseasesEmily A Largent, Steven D Pearson
Journal of Medical Ethics|October 14, 2020
Compensating for research risk: permissible but not obligatoryHolly Fernandez Lynch, Emily A Largent
JAMA Neurology|February 19, 2024
Diagnosing Preclinical and Prodromal Neurodegenerative Diseases-The Clinical Is PoliticalClaire M Erickson, Emily A Largent
Clinical Trials (London, England)|December 21, 2018
Making the case for completion bonuses in clinical trialsEmily A Largent, Holly Fernandez Lynch
JAMA Neurology|January 4, 2022
Bringing Alzheimer Disease Testing and Results Disclosure Into the 21st Century Cures ActEmily A Largent, Angela R Bradbury
Perspectives in Biology and Medicine|November 29, 2021
The Legality and Ethics of Mandating COVID-19 VaccinationEmily A Largent, Franklin G Miller
Yale Journal of Health Policy, Law, and Ethics|December 19, 2017
Paying Research Participants: Regulatory Uncertainty, Conceptual Confusion, and a Path ForwardEmily A Largent, Holly Fernandez Lynch
The Journal of Infectious Diseases|May 30, 2020
Paying Participants in COVID-19 TrialsEmily A Largent, Holly Fernandez Lynch
BMJ (Clinical Research Ed.)|June 8, 2023
Considering tomorrow's patients in today's drug approvalsHolly Fernandez Lynch, Emily A Largent
The Hastings Center Report|April 11, 2021
Public Attitudes toward Consent When Research Is Integrated into Care-Any "Ought" from All the "Is"?Stephanie R Morain, Emily A Largent
Pageof 18