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Deborah A Zarin

Showing results (41-50 of 67) with videos related to

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The New England Journal of Medicine|September 17, 2016
Trial Reporting in ClinicalTrials.gov - The Final RuleDeborah A Zarin, Tony Tse, Rebecca J Williams, et al.
Med (New York, N.Y.)|April 15, 2023
How to limit uninformative trials: Results from a Delphi working groupLuke Gelinas, Nora Hutchinson, Deborah A Zarin, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|July 21, 2010
Registration of observational studies: is it time?Rebecca J Williams, Tony Tse, William R Harlan, et al.
Archives of Surgery (Chicago, Ill. : 1960)|March 4, 2003
Hyperbaric oxygen for treating wounds: a systematic review of the literatureChenchen Wang, Steven Schwaitzberg, Elise Berliner, et al.
The American Journal of Bioethics : AJOB|November 27, 2018
Universal Funder Responsibilities That Advance Social ValueBarbara E Bierer, David H Strauss, Sarah A White, et al.
Annals of Internal Medicine|June 14, 2016
ClinicalTrials.gov and Drugs@FDA: A Comparison of Results Reporting for New Drug Approval TrialsLisa M Schwartz, Steven Woloshin, Eugene Zheng, et al.
JAMA|March 30, 2023
Comparison of Availability of Trial Results in ClinicalTrials.gov and PubMed by Data Source and Funder TypeJulianne T Nelson, Tony Tse, Yvonne Puplampu-Dove, et al.
JAMA Network Open|November 18, 2021
Characterization of Informed Consent Forms Posted on ClinicalTrials.govTony Tse, Sarah White, Luke Gelinas, et al.
JAMA Internal Medicine|March 14, 2018
Results Reporting for Trials With the Same Sponsor, Drug, and Condition in ClinicalTrials.gov and Peer-Reviewed PublicationsKevin M Fain, Thiyagu Rajakannan, Tony Tse, et al.
Journal of Clinical and Translational Science|September 25, 2023
Characterization of key information sections in informed consent forms posted on ClinicalTrials.govLuke Gelinas, Walker Morrell, Tony Tse, et al.
Pageof 7

Showing results (41-50 of 67) with videos related to

Sort By:
Pageof 7
The New England Journal of Medicine|September 17, 2016
Trial Reporting in ClinicalTrials.gov - The Final RuleDeborah A Zarin, Tony Tse, Rebecca J Williams, et al.
Med (New York, N.Y.)|April 15, 2023
How to limit uninformative trials: Results from a Delphi working groupLuke Gelinas, Nora Hutchinson, Deborah A Zarin, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|July 21, 2010
Registration of observational studies: is it time?Rebecca J Williams, Tony Tse, William R Harlan, et al.
Archives of Surgery (Chicago, Ill. : 1960)|March 4, 2003
Hyperbaric oxygen for treating wounds: a systematic review of the literatureChenchen Wang, Steven Schwaitzberg, Elise Berliner, et al.
The American Journal of Bioethics : AJOB|November 27, 2018
Universal Funder Responsibilities That Advance Social ValueBarbara E Bierer, David H Strauss, Sarah A White, et al.
Annals of Internal Medicine|June 14, 2016
ClinicalTrials.gov and Drugs@FDA: A Comparison of Results Reporting for New Drug Approval TrialsLisa M Schwartz, Steven Woloshin, Eugene Zheng, et al.
JAMA|March 30, 2023
Comparison of Availability of Trial Results in ClinicalTrials.gov and PubMed by Data Source and Funder TypeJulianne T Nelson, Tony Tse, Yvonne Puplampu-Dove, et al.
JAMA Network Open|November 18, 2021
Characterization of Informed Consent Forms Posted on ClinicalTrials.govTony Tse, Sarah White, Luke Gelinas, et al.
JAMA Internal Medicine|March 14, 2018
Results Reporting for Trials With the Same Sponsor, Drug, and Condition in ClinicalTrials.gov and Peer-Reviewed PublicationsKevin M Fain, Thiyagu Rajakannan, Tony Tse, et al.
Journal of Clinical and Translational Science|September 25, 2023
Characterization of key information sections in informed consent forms posted on ClinicalTrials.govLuke Gelinas, Walker Morrell, Tony Tse, et al.
Pageof 7