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Julie De Backer

Showing results (41-50 of 208) with videos related to

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Polskie Archiwum Medycyny Wewnetrznej|December 18, 2013
New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissectionsLaurence Campens, Marjolijn Renard, Bert Callewaert, et al.
Acta Cardiologica|May 3, 2014
Treatment of pre-existing cardiomyopathy during pregnancySofie Gevaert, Michel De Pauw, Fiona Tromp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 18, 2006
A critical analysis of minor cardiovascular criteria in the diagnostic evaluation of patients with Marfan syndromeJulie De Backer, Bart Loeys, Dan Devos, et al.
Aorta (Stamford, Conn.)|January 23, 2016
Genes in Thoracic Aortic Aneurysms and Dissections - Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical PracticeJulie De Backer, Marjolijn Renard, Laurence Campens, et al.
European Journal of Pediatrics|June 23, 2023
Preferences for disease-related information and transitional skills among adolescents with congenital heart disease in the early transitional stageMichèle de Hosson, Katya De Groote, Herlinde Wynendaele, et al.
IEEE Transactions on Bio-Medical Engineering|April 29, 2008
Effect of an abdominal aortic aneurysm on wave reflection in the aortaAbigail Swillens, Lieve Lanoye, Julie De Backer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 6, 2014
Loeys-Dietz syndrome is a specific phenotype and not a concomitant of any mutation in a gene involved in TGF-β signalingReed Pyeritz, Guillaume Jondeau, Rocio Moran, et al.
Acta Cardiologica|June 29, 2017
Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome: a randomized, double-blind clinical trialLaura Muiño-Mosquera, Sylvia De Nobele, Daniel Devos, et al.
IEEE Transactions on Bio-Medical Engineering|April 5, 2023
Fluid-Structure Interaction Modeling of the Aortic Hemodynamics in Adult Zebrafish: A Pilot Study Based on Synchrotron X-Ray TomographyMatthias Van Impe, Lisa Caboor, Violette Deleeuw, et al.
Journal of Pediatric Nursing|April 3, 2021
Needs and Experiences of Adolescents with Congenital Heart Disease and Parents in the Transitional Process: A Qualitative StudyMichèle de Hosson, Peter J J Goossens, Julie De Backer, et al.
Pageof 21

Showing results (41-50 of 208) with videos related to

Sort By:
Pageof 21
Polskie Archiwum Medycyny Wewnetrznej|December 18, 2013
New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissectionsLaurence Campens, Marjolijn Renard, Bert Callewaert, et al.
Acta Cardiologica|May 3, 2014
Treatment of pre-existing cardiomyopathy during pregnancySofie Gevaert, Michel De Pauw, Fiona Tromp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 18, 2006
A critical analysis of minor cardiovascular criteria in the diagnostic evaluation of patients with Marfan syndromeJulie De Backer, Bart Loeys, Dan Devos, et al.
Aorta (Stamford, Conn.)|January 23, 2016
Genes in Thoracic Aortic Aneurysms and Dissections - Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical PracticeJulie De Backer, Marjolijn Renard, Laurence Campens, et al.
European Journal of Pediatrics|June 23, 2023
Preferences for disease-related information and transitional skills among adolescents with congenital heart disease in the early transitional stageMichèle de Hosson, Katya De Groote, Herlinde Wynendaele, et al.
IEEE Transactions on Bio-Medical Engineering|April 29, 2008
Effect of an abdominal aortic aneurysm on wave reflection in the aortaAbigail Swillens, Lieve Lanoye, Julie De Backer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 6, 2014
Loeys-Dietz syndrome is a specific phenotype and not a concomitant of any mutation in a gene involved in TGF-β signalingReed Pyeritz, Guillaume Jondeau, Rocio Moran, et al.
Acta Cardiologica|June 29, 2017
Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome: a randomized, double-blind clinical trialLaura Muiño-Mosquera, Sylvia De Nobele, Daniel Devos, et al.
IEEE Transactions on Bio-Medical Engineering|April 5, 2023
Fluid-Structure Interaction Modeling of the Aortic Hemodynamics in Adult Zebrafish: A Pilot Study Based on Synchrotron X-Ray TomographyMatthias Van Impe, Lisa Caboor, Violette Deleeuw, et al.
Journal of Pediatric Nursing|April 3, 2021
Needs and Experiences of Adolescents with Congenital Heart Disease and Parents in the Transitional Process: A Qualitative StudyMichèle de Hosson, Peter J J Goossens, Julie De Backer, et al.
Pageof 21