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Damien Bonnet

Showing results (401-410 of 461) with videos related to

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The European Respiratory Journal|March 21, 2024
Pulmonary vascular phenotype identified in patients with <i>GDF2</i> (<i>BMP9</i>) or <i>BMP10</i> variants: an international multicentre studyJulien Grynblat, Harm Jan Bogaard, Mélanie Eyries, et al.
Journal of the American College of Cardiology|April 1, 2017
Autosomal Recessive Cardiomyopathy Presenting as Acute MyocarditisSerkan Belkaya, Amy R Kontorovich, Minji Byun, et al.
The Journal of Pediatrics|September 18, 2010
Isolated congenital asplenia: a French nationwide retrospective survey of 20 casesNizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, et al.
Archives of Cardiovascular Diseases|April 13, 2021
Catheter ablation in adults with congenital heart disease: A 15-year perspective from a tertiary centreVictor Waldmann, Denis Amet, Alexandre Zhao, et al.
Orphanet Journal of Rare Diseases|May 10, 2013
Natural history of Barth syndrome: a national cohort study of 22 patientsCharlotte Rigaud, Anne-Sophie Lebre, Renaud Touraine, et al.
Journal of the American Heart Association|July 9, 2024
Pulmonary Hypertension Induced by Right Pulmonary Artery Occlusion: Hemodynamic Consequences of <i>Bmpr2</i> MutationAlban Todesco, Julien Grynblat, Kouamé Kan Firmin Akoumia, et al.
The European Respiratory Journal|May 26, 2022
An emerging phenotype of pulmonary arterial hypertension patients carrying <i>SOX17</i> variantsDavid Montani, Benoit Lechartier, Barbara Girerd, et al.
The Journal of Rheumatology|May 2, 2022
Health Outcomes of 215 Mothers of Children With Autoimmune Congenital Heart Block: Analysis of the French Neonatal Lupus Syndrome RegistryImene Miniaoui, Nathalie Morel, Kateri Lévesque, et al.
The European Respiratory Journal|February 22, 2020
Phenotype and outcome of pulmonary arterial hypertension patients carrying a <i>TBX4</i> mutationPierre Thoré, Barbara Girerd, Xavier Jaïs, et al.
Respiratory Medicine and Research|May 11, 2026
The preponderance of genetic variations in paediatric pulmonary hypertensionJulien Grynblat, Mélanie Eyries, Marine Ambar-Akkaoui, et al.
Pageof 47

Showing results (401-410 of 461) with videos related to

Sort By:
Pageof 47
The European Respiratory Journal|March 21, 2024
Pulmonary vascular phenotype identified in patients with <i>GDF2</i> (<i>BMP9</i>) or <i>BMP10</i> variants: an international multicentre studyJulien Grynblat, Harm Jan Bogaard, Mélanie Eyries, et al.
Journal of the American College of Cardiology|April 1, 2017
Autosomal Recessive Cardiomyopathy Presenting as Acute MyocarditisSerkan Belkaya, Amy R Kontorovich, Minji Byun, et al.
The Journal of Pediatrics|September 18, 2010
Isolated congenital asplenia: a French nationwide retrospective survey of 20 casesNizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, et al.
Archives of Cardiovascular Diseases|April 13, 2021
Catheter ablation in adults with congenital heart disease: A 15-year perspective from a tertiary centreVictor Waldmann, Denis Amet, Alexandre Zhao, et al.
Orphanet Journal of Rare Diseases|May 10, 2013
Natural history of Barth syndrome: a national cohort study of 22 patientsCharlotte Rigaud, Anne-Sophie Lebre, Renaud Touraine, et al.
Journal of the American Heart Association|July 9, 2024
Pulmonary Hypertension Induced by Right Pulmonary Artery Occlusion: Hemodynamic Consequences of <i>Bmpr2</i> MutationAlban Todesco, Julien Grynblat, Kouamé Kan Firmin Akoumia, et al.
The European Respiratory Journal|May 26, 2022
An emerging phenotype of pulmonary arterial hypertension patients carrying <i>SOX17</i> variantsDavid Montani, Benoit Lechartier, Barbara Girerd, et al.
The Journal of Rheumatology|May 2, 2022
Health Outcomes of 215 Mothers of Children With Autoimmune Congenital Heart Block: Analysis of the French Neonatal Lupus Syndrome RegistryImene Miniaoui, Nathalie Morel, Kateri Lévesque, et al.
The European Respiratory Journal|February 22, 2020
Phenotype and outcome of pulmonary arterial hypertension patients carrying a <i>TBX4</i> mutationPierre Thoré, Barbara Girerd, Xavier Jaïs, et al.
Respiratory Medicine and Research|May 11, 2026
The preponderance of genetic variations in paediatric pulmonary hypertensionJulien Grynblat, Mélanie Eyries, Marine Ambar-Akkaoui, et al.
Pageof 47