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Marjolijn Renard

Showing results (11-20 of 37) with videos related to

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Current Pharmaceutical Design|August 27, 2015
Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and DissectionsJulie De Backer, Marjolijn Renard, Laurence Campens, et al.
Frontiers in Pharmacology|September 28, 2020
MEK1/2 Inhibition in Murine Heart and Aorta After Oral Administration of Refametinib Supplemented Drinking WaterFelke Steijns, Nathalie Bracke, Marjolijn Renard, et al.
Plos One|May 15, 2018
Correction: Sex, pregnancy and aortic disease in Marfan syndromeMarjolijn Renard, Laura Muiño-Mosquera, Elise C Manalo, et al.
Pediatric Research|June 5, 2015
Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humansLaurence Campens, Marjolijn Renard, Bram Trachet, et al.
Plos One|July 15, 2017
Sex, pregnancy and aortic disease in Marfan syndromeMarjolijn Renard, Laura Muiño-Mosquera, Elise C Manalo, et al.
Sensors (Basel, Switzerland)|July 16, 2020
Ambulatory Electrocardiographic Monitoring and Ectopic Beat Detection in Conscious MiceFelke Steijns, Máté I Tóth, Anthony Demolder, et al.
International Journal of Molecular Sciences|September 29, 2020
Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan SyndromeFelke Steijns, Marjolijn Renard, Marine Vanhomwegen, et al.
Clinical Dysmorphology|March 24, 2010
Short stature, severe aortic root dilation, skin hyperextensibility, extreme joint laxity and craniofacial dysmorphic features: a probable new syndromeElke Verstraeten, Sofie Symoens, Marjolijn Renard, et al.
Circulation. Genomic and Precision Medicine|June 8, 2018
Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines for the Interpretation of Sequenced Variants in the <i>FBN1</i> Gene for Marfan Syndrome: Proposal for a Disease- and Gene-Specific GuidelineLaura Muiño-Mosquera, Felke Steijns, Tjorven Audenaert, et al.
International Journal of Cardiology|January 18, 2011
The Ghent Marfan Trial--a randomized, double-blind placebo controlled trial with losartan in Marfan patients treated with β-blockersKatarina Möberg, Sylvia De Nobele, Dan Devos, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Current Pharmaceutical Design|August 27, 2015
Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and DissectionsJulie De Backer, Marjolijn Renard, Laurence Campens, et al.
Frontiers in Pharmacology|September 28, 2020
MEK1/2 Inhibition in Murine Heart and Aorta After Oral Administration of Refametinib Supplemented Drinking WaterFelke Steijns, Nathalie Bracke, Marjolijn Renard, et al.
Plos One|May 15, 2018
Correction: Sex, pregnancy and aortic disease in Marfan syndromeMarjolijn Renard, Laura Muiño-Mosquera, Elise C Manalo, et al.
Pediatric Research|June 5, 2015
Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humansLaurence Campens, Marjolijn Renard, Bram Trachet, et al.
Plos One|July 15, 2017
Sex, pregnancy and aortic disease in Marfan syndromeMarjolijn Renard, Laura Muiño-Mosquera, Elise C Manalo, et al.
Sensors (Basel, Switzerland)|July 16, 2020
Ambulatory Electrocardiographic Monitoring and Ectopic Beat Detection in Conscious MiceFelke Steijns, Máté I Tóth, Anthony Demolder, et al.
International Journal of Molecular Sciences|September 29, 2020
Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan SyndromeFelke Steijns, Marjolijn Renard, Marine Vanhomwegen, et al.
Clinical Dysmorphology|March 24, 2010
Short stature, severe aortic root dilation, skin hyperextensibility, extreme joint laxity and craniofacial dysmorphic features: a probable new syndromeElke Verstraeten, Sofie Symoens, Marjolijn Renard, et al.
Circulation. Genomic and Precision Medicine|June 8, 2018
Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines for the Interpretation of Sequenced Variants in the <i>FBN1</i> Gene for Marfan Syndrome: Proposal for a Disease- and Gene-Specific GuidelineLaura Muiño-Mosquera, Felke Steijns, Tjorven Audenaert, et al.
International Journal of Cardiology|January 18, 2011
The Ghent Marfan Trial--a randomized, double-blind placebo controlled trial with losartan in Marfan patients treated with β-blockersKatarina Möberg, Sylvia De Nobele, Dan Devos, et al.
Pageof 4