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Ida Sim

Showing results (51-60 of 115) with videos related to

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Lancet (London, England)|May 23, 2006
Clinical trial registration: transparency is the watchwordIda Sim, An-Wen Chan, A Metin Gülmezoglu, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|December 5, 2013
Tools for Identifying Reliable Evidence and Implementing it in Everyday Clinical CareAaron M Cohen, Dina Demner-Fushman, Alfonso Iorio, et al.
Journal of Biomedical Informatics|October 25, 2022
Ontology-based categorization of clinical studies by their conditionsHao Liu, Simona Carini, Zhehuan Chen, et al.
Trials|February 19, 2021
COVID-19 trials: declarations of data sharing intentions at trial registration and at publicationRebecca Li, Megan von Isenburg, Marcia Levenstein, et al.
BMJ (Clinical Research Ed.)|April 23, 2005
Principles for international registration of protocol information and results from human trials of health related interventions: Ottawa statement (part 1)Karmela Krleza-Jerić, An-Wen Chan, Kay Dickersin, et al.
Revista Panamericana De Salud Publica = Pan American Journal of Public Health|September 14, 2006
[Principles of the international registry of protocols and clinical trial results based on health interventions in human beings: Ottawa Declaration (part 1)]Karmela Krleza-Jerić, An-Wen Chan, Kay Dickersin, et al.
Science (New York, N.Y.)|February 7, 2009
Keeping raw data in contextIda Sim, Christopher G Chute, Harold Lehmann, et al.
BMJ Open|October 30, 2020
Timely access to trial data in the context of a pandemic: the time is nowRebecca Li, Julie Wood, Amrutha Baskaran, et al.
Journal of Biomedical Informatics|January 29, 2016
Multivariate analysis of the population representativeness of related clinical studiesZhe He, Patrick Ryan, Julia Hoxha, et al.
BMC Medicine|July 18, 2019
Why we need a small data paradigmEric B Hekler, Predrag Klasnja, Guillaume Chevance, et al.
Pageof 12

Showing results (51-60 of 115) with videos related to

Sort By:
Pageof 12
Lancet (London, England)|May 23, 2006
Clinical trial registration: transparency is the watchwordIda Sim, An-Wen Chan, A Metin Gülmezoglu, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|December 5, 2013
Tools for Identifying Reliable Evidence and Implementing it in Everyday Clinical CareAaron M Cohen, Dina Demner-Fushman, Alfonso Iorio, et al.
Journal of Biomedical Informatics|October 25, 2022
Ontology-based categorization of clinical studies by their conditionsHao Liu, Simona Carini, Zhehuan Chen, et al.
Trials|February 19, 2021
COVID-19 trials: declarations of data sharing intentions at trial registration and at publicationRebecca Li, Megan von Isenburg, Marcia Levenstein, et al.
BMJ (Clinical Research Ed.)|April 23, 2005
Principles for international registration of protocol information and results from human trials of health related interventions: Ottawa statement (part 1)Karmela Krleza-Jerić, An-Wen Chan, Kay Dickersin, et al.
Revista Panamericana De Salud Publica = Pan American Journal of Public Health|September 14, 2006
[Principles of the international registry of protocols and clinical trial results based on health interventions in human beings: Ottawa Declaration (part 1)]Karmela Krleza-Jerić, An-Wen Chan, Kay Dickersin, et al.
Science (New York, N.Y.)|February 7, 2009
Keeping raw data in contextIda Sim, Christopher G Chute, Harold Lehmann, et al.
BMJ Open|October 30, 2020
Timely access to trial data in the context of a pandemic: the time is nowRebecca Li, Julie Wood, Amrutha Baskaran, et al.
Journal of Biomedical Informatics|January 29, 2016
Multivariate analysis of the population representativeness of related clinical studiesZhe He, Patrick Ryan, Julia Hoxha, et al.
BMC Medicine|July 18, 2019
Why we need a small data paradigmEric B Hekler, Predrag Klasnja, Guillaume Chevance, et al.
Pageof 12