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Debray

Showing results (621-630 of 938) with videos related to

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European Journal of Radiology|December 27, 2014
Interstitial lung disease in anti-synthetase syndrome: initial and follow-up CT findingsMarie-Pierre Debray, Raphael Borie, Marie-Pierre Revel, et al.
The European Respiratory Journal|March 17, 2017
Early computed tomography modifications following bronchial thermoplasty in patients with severe asthmaMarie-Pierre Debray, Marie-Christine Dombret, Marina Pretolani, et al.
European Journal of Preventive Cardiology|December 12, 2023
The potential benefit of statin prescription based on prediction of treatment responsiveness in older individuals: an application to the PROSPER randomized controlled trialTri-Long Nguyen, Stella Trompet, John B Brodersen, et al.
Research Synthesis Methods|January 13, 2016
GetReal in network meta-analysis: a review of the methodologyOrestis Efthimiou, Thomas P A Debray, Gert van Valkenhoef, et al.
ERJ Open Research|May 25, 2023
<i>NKX2.1</i> mutation revealed by a lymphoid interstitial pneumonia in an adult with rheumatoid arthritisPierre Le Guen, Raphael Borie, Marie Legendre, et al.
Plos One|January 24, 2013
Detection of alveolar fibrocytes in idiopathic pulmonary fibrosis and systemic sclerosisRaphael Borie, Christophe Quesnel, Sophie Phin, et al.
Pediatric Transplantation|October 26, 2018
Comparative pharmacokinetics of tacrolimus in de novo pediatric transplant recipients randomized to receive immediate- or prolonged-release tacrolimusKarel Vondrak, Anil Dhawan, Francesco Parisi, et al.
Annales De L'Anesthesiologie Francaise|January 1, 1980
[Neonatal hernias of the dome of the diaphragm. Why a gloomy prognosis?]M Cloup, D Pellerin, J C Mselati, et al.
Joint Bone Spine|September 24, 2016
Cystic lung disease in Sjögren's syndrome: An observational studySarah Lechtman, Marie-Pierre Debray, Bruno Crestani, et al.
Journal of Medical Genetics|November 4, 2008
Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15F-G Debray, M Lambert, B Lemieux, et al.
Pageof 94

Showing results (621-630 of 938) with videos related to

Sort By:
Pageof 94
European Journal of Radiology|December 27, 2014
Interstitial lung disease in anti-synthetase syndrome: initial and follow-up CT findingsMarie-Pierre Debray, Raphael Borie, Marie-Pierre Revel, et al.
The European Respiratory Journal|March 17, 2017
Early computed tomography modifications following bronchial thermoplasty in patients with severe asthmaMarie-Pierre Debray, Marie-Christine Dombret, Marina Pretolani, et al.
European Journal of Preventive Cardiology|December 12, 2023
The potential benefit of statin prescription based on prediction of treatment responsiveness in older individuals: an application to the PROSPER randomized controlled trialTri-Long Nguyen, Stella Trompet, John B Brodersen, et al.
Research Synthesis Methods|January 13, 2016
GetReal in network meta-analysis: a review of the methodologyOrestis Efthimiou, Thomas P A Debray, Gert van Valkenhoef, et al.
ERJ Open Research|May 25, 2023
<i>NKX2.1</i> mutation revealed by a lymphoid interstitial pneumonia in an adult with rheumatoid arthritisPierre Le Guen, Raphael Borie, Marie Legendre, et al.
Plos One|January 24, 2013
Detection of alveolar fibrocytes in idiopathic pulmonary fibrosis and systemic sclerosisRaphael Borie, Christophe Quesnel, Sophie Phin, et al.
Pediatric Transplantation|October 26, 2018
Comparative pharmacokinetics of tacrolimus in de novo pediatric transplant recipients randomized to receive immediate- or prolonged-release tacrolimusKarel Vondrak, Anil Dhawan, Francesco Parisi, et al.
Annales De L'Anesthesiologie Francaise|January 1, 1980
[Neonatal hernias of the dome of the diaphragm. Why a gloomy prognosis?]M Cloup, D Pellerin, J C Mselati, et al.
Joint Bone Spine|September 24, 2016
Cystic lung disease in Sjögren's syndrome: An observational studySarah Lechtman, Marie-Pierre Debray, Bruno Crestani, et al.
Journal of Medical Genetics|November 4, 2008
Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15F-G Debray, M Lambert, B Lemieux, et al.
Pageof 94