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JAMA Internal Medicine
|
September 28, 2020
Assessment of Data Sources That Support US Food and Drug Administration Medical Devices Safety Communications
Noam Tau, Daniel Shepshelovich
Oncotarget
|
August 21, 2018
Expedited approval of cancer drugs without randomized controlled trials: Too good to be true?
Daniel Shepshelovich, Eitan Amir
JAMA Internal Medicine
|
December 20, 2021
Emergency Use Authorizations of COVID-19-Related Medical Products
Itay Moshkovits, Daniel Shepshelovich
Human Vaccines & Immunotherapeutics
|
December 3, 2020
Vaccine safety - is the SARS-CoV-2 vaccine any different?
Noam Tau, Dafna Yahav, Daniel Shepshelovich
Harefuah
|
September 9, 2005
[Accelerated atherosclerosis in rheumatoid arthritis]
Daniel Shepshelovich, Yaniv Sherer, Yehuda Shoenfeld
The Israel Medical Association Journal : IMAJ
|
November 27, 2022
Predicting Which Patients Are at Risk for Clinical Deterioration in COVID-19: A Review of the Current Models in Use
Michael Shapiro, Yarden Yavne, Daniel Shepshelovich
Leukemia & Lymphoma
|
May 26, 2020
Changes in primary outcome and sample size measures after initiation of accrual among trials supporting approval of drugs for hematological malignancies by the US food and drug administration
Irina Amitai, Pia Raanani, Daniel Shepshelovich
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
April 28, 2020
Assessment of Data Supporting the Efficacy of New Antibiotics for Treating Infections Caused by Multidrug-resistant Bacteria
Dafna Yahav, Noam Tau, Daniel Shepshelovich
Annals of Internal Medicine
|
July 28, 2020
Postmarketing Safety of Vaccines Approved by the U.S. Food and Drug Administration : A Cohort Study
Noam Tau, Dafna Yahav, Daniel Shepshelovich
Infectious Diseases and Therapy
|
February 17, 2021
Cost Analysis of New Antibiotics to Treat Multidrug-Resistant Bacterial Infections: Mind the Gap
Dafna Yahav, Daniel Shepshelovich, Noam Tau
Page
of 10
Search research articles
Search
Showing results (1-10 of 93) with videos related to
Sort By:
Page
of 10
JAMA Internal Medicine
|
September 28, 2020
Assessment of Data Sources That Support US Food and Drug Administration Medical Devices Safety Communications
Noam Tau, Daniel Shepshelovich
Oncotarget
|
August 21, 2018
Expedited approval of cancer drugs without randomized controlled trials: Too good to be true?
Daniel Shepshelovich, Eitan Amir
JAMA Internal Medicine
|
December 20, 2021
Emergency Use Authorizations of COVID-19-Related Medical Products
Itay Moshkovits, Daniel Shepshelovich
Human Vaccines & Immunotherapeutics
|
December 3, 2020
Vaccine safety - is the SARS-CoV-2 vaccine any different?
Noam Tau, Dafna Yahav, Daniel Shepshelovich
Harefuah
|
September 9, 2005
[Accelerated atherosclerosis in rheumatoid arthritis]
Daniel Shepshelovich, Yaniv Sherer, Yehuda Shoenfeld
The Israel Medical Association Journal : IMAJ
|
November 27, 2022
Predicting Which Patients Are at Risk for Clinical Deterioration in COVID-19: A Review of the Current Models in Use
Michael Shapiro, Yarden Yavne, Daniel Shepshelovich
Leukemia & Lymphoma
|
May 26, 2020
Changes in primary outcome and sample size measures after initiation of accrual among trials supporting approval of drugs for hematological malignancies by the US food and drug administration
Irina Amitai, Pia Raanani, Daniel Shepshelovich
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
April 28, 2020
Assessment of Data Supporting the Efficacy of New Antibiotics for Treating Infections Caused by Multidrug-resistant Bacteria
Dafna Yahav, Noam Tau, Daniel Shepshelovich
Annals of Internal Medicine
|
July 28, 2020
Postmarketing Safety of Vaccines Approved by the U.S. Food and Drug Administration : A Cohort Study
Noam Tau, Dafna Yahav, Daniel Shepshelovich
Infectious Diseases and Therapy
|
February 17, 2021
Cost Analysis of New Antibiotics to Treat Multidrug-Resistant Bacterial Infections: Mind the Gap
Dafna Yahav, Daniel Shepshelovich, Noam Tau
Page
of 10