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Thomas P Gross

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

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Circulation|February 16, 2006
Postmarket surveillance for drug-eluting coronary stents: a comprehensive approachDonald S Baim, Roxana Mehran, Dean J Kereiakes, et al.
JAMA|April 28, 2006
Pacemaker and ICD generator malfunctions: analysis of Food and Drug Administration annual reportsWilliam H Maisel, Megan Moynahan, Bram D Zuckerman, et al.
Pharmacoepidemiology and Drug Safety|January 21, 2012
The US Food and Drug Administration's Sentinel Initiative: expanding the horizons of medical product safetyMelissa A Robb, Judith A Racoosin, Rachel E Sherman, et al.
JAMA|November 11, 2010
Automated surveillance to detect postprocedure safety signals of approved cardiovascular devicesFrederic S Resnic, Thomas P Gross, Danica Marinac-Dabic, et al.
The Journal of Bone and Joint Surgery. American Volume|November 10, 2012
Risk of revision for fixed versus mobile-bearing primary total knee replacementsRobert S Namba, Maria C S Inacio, Elizabeth W Paxton, et al.
BMC Medical Informatics and Decision Making|December 16, 2011
Evaluation of an automated safety surveillance system using risk adjusted sequential probability ratio testingMichael E Matheny, Sharon-Lise T Normand, Thomas P Gross, et al.
JAMA Internal Medicine|February 20, 2013
Sex and risk of hip implant failure: assessing total hip arthroplasty outcomes in the United StatesMaria C S Inacio, Christopher F Ake, Elizabeth W Paxton, et al.
The Annals of Thoracic Surgery|July 28, 2012
Long-term outcomes after transmyocardial revascularizationDale R Tavris, James Matthew Brennan, Art Sedrakyan, et al.
Medical Care|February 15, 2013
Feasibility of proactive medical device surveillance: the VA Clinical Assessment Reporting and Tracking (CART) programThomas T Tsai, Tamara L Box, Hans Gethoffer, et al.
American Heart Journal|July 29, 2008
Postmarket evaluation of breakthrough technologiesSunil V Rao, Robert M Califf, Judith M Kramer, et al.
Pageof 5

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

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Circulation|February 16, 2006
Postmarket surveillance for drug-eluting coronary stents: a comprehensive approachDonald S Baim, Roxana Mehran, Dean J Kereiakes, et al.
JAMA|April 28, 2006
Pacemaker and ICD generator malfunctions: analysis of Food and Drug Administration annual reportsWilliam H Maisel, Megan Moynahan, Bram D Zuckerman, et al.
Pharmacoepidemiology and Drug Safety|January 21, 2012
The US Food and Drug Administration's Sentinel Initiative: expanding the horizons of medical product safetyMelissa A Robb, Judith A Racoosin, Rachel E Sherman, et al.
JAMA|November 11, 2010
Automated surveillance to detect postprocedure safety signals of approved cardiovascular devicesFrederic S Resnic, Thomas P Gross, Danica Marinac-Dabic, et al.
The Journal of Bone and Joint Surgery. American Volume|November 10, 2012
Risk of revision for fixed versus mobile-bearing primary total knee replacementsRobert S Namba, Maria C S Inacio, Elizabeth W Paxton, et al.
BMC Medical Informatics and Decision Making|December 16, 2011
Evaluation of an automated safety surveillance system using risk adjusted sequential probability ratio testingMichael E Matheny, Sharon-Lise T Normand, Thomas P Gross, et al.
JAMA Internal Medicine|February 20, 2013
Sex and risk of hip implant failure: assessing total hip arthroplasty outcomes in the United StatesMaria C S Inacio, Christopher F Ake, Elizabeth W Paxton, et al.
The Annals of Thoracic Surgery|July 28, 2012
Long-term outcomes after transmyocardial revascularizationDale R Tavris, James Matthew Brennan, Art Sedrakyan, et al.
Medical Care|February 15, 2013
Feasibility of proactive medical device surveillance: the VA Clinical Assessment Reporting and Tracking (CART) programThomas T Tsai, Tamara L Box, Hans Gethoffer, et al.
American Heart Journal|July 29, 2008
Postmarket evaluation of breakthrough technologiesSunil V Rao, Robert M Califf, Judith M Kramer, et al.
Pageof 5