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Franz Koenig

Showing results (31-40 of 64) with videos related to

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Statistics in Medicine|May 19, 2025
Closed MCP-Mod for Pairwise Comparisons of Several Doses With a ControlFranz Koenig, Sergey Krasnozhon, Bjoern Bornkamp, et al.
Hepatology (Baltimore, Md.)|September 27, 2003
Survival in patients undergoing transjugular intrahepatic portosystemic shunt: ePTFE-covered stentgrafts versus bare stentsBernhard Angermayr, Manfred Cejna, Franz Koenig, et al.
Trials|June 15, 2023
On the use of non-concurrent controls in platform trials: a scoping reviewMarta Bofill Roig, Cora Burgwinkel, Ursula Garczarek, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|May 25, 2019
Composite Outcome Improves Feasibility of Clinical Trials in Peritoneal DialysisMichael Boehm, Julia Niewczas, Harald Herkner, et al.
Biometrical Journal. Biometrische Zeitschrift|June 20, 2014
Sharing clinical trial data on patient level: opportunities and challengesFranz Koenig, Jim Slattery, Trish Groves, et al.
Paediatric Anaesthesia|January 20, 2011
Role of modeling and simulation in pediatric investigation plansEfthymios Manolis, Tariq Eldirdiry Osman, Ralf Herold, et al.
Trials|October 4, 2014
Adaptive clinical trial designs for European marketing authorization: a survey of scientific advice letters from the European Medicines AgencyAmelie Elsäßer, Jan Regnstrom, Thorsten Vetter, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|August 1, 2007
An integrated MELD model including serum sodium and age improves the prediction of early mortality in patients with cirrhosisAngelo Luca, Berhard Angermayr, Guido Bertolini, et al.
European Journal of Clinical Pharmacology|November 26, 2009
Factors associated with success of market authorisation applications for pharmaceutical drugs submitted to the European Medicines AgencyJan Regnstrom, Franz Koenig, Bo Aronsson, et al.
Drug Discovery Today|October 28, 2017
Marketing authorisation of orphan medicines in Europe from 2000 to 2013Matthias P Hofer, Hanna Hedman, Maria Mavris, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Statistics in Medicine|May 19, 2025
Closed MCP-Mod for Pairwise Comparisons of Several Doses With a ControlFranz Koenig, Sergey Krasnozhon, Bjoern Bornkamp, et al.
Hepatology (Baltimore, Md.)|September 27, 2003
Survival in patients undergoing transjugular intrahepatic portosystemic shunt: ePTFE-covered stentgrafts versus bare stentsBernhard Angermayr, Manfred Cejna, Franz Koenig, et al.
Trials|June 15, 2023
On the use of non-concurrent controls in platform trials: a scoping reviewMarta Bofill Roig, Cora Burgwinkel, Ursula Garczarek, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|May 25, 2019
Composite Outcome Improves Feasibility of Clinical Trials in Peritoneal DialysisMichael Boehm, Julia Niewczas, Harald Herkner, et al.
Biometrical Journal. Biometrische Zeitschrift|June 20, 2014
Sharing clinical trial data on patient level: opportunities and challengesFranz Koenig, Jim Slattery, Trish Groves, et al.
Paediatric Anaesthesia|January 20, 2011
Role of modeling and simulation in pediatric investigation plansEfthymios Manolis, Tariq Eldirdiry Osman, Ralf Herold, et al.
Trials|October 4, 2014
Adaptive clinical trial designs for European marketing authorization: a survey of scientific advice letters from the European Medicines AgencyAmelie Elsäßer, Jan Regnstrom, Thorsten Vetter, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|August 1, 2007
An integrated MELD model including serum sodium and age improves the prediction of early mortality in patients with cirrhosisAngelo Luca, Berhard Angermayr, Guido Bertolini, et al.
European Journal of Clinical Pharmacology|November 26, 2009
Factors associated with success of market authorisation applications for pharmaceutical drugs submitted to the European Medicines AgencyJan Regnstrom, Franz Koenig, Bo Aronsson, et al.
Drug Discovery Today|October 28, 2017
Marketing authorisation of orphan medicines in Europe from 2000 to 2013Matthias P Hofer, Hanna Hedman, Maria Mavris, et al.
Pageof 7