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Damien Bonnet

Showing results (391-400 of 461) with videos related to

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Plos One|September 17, 2025
Diagnostic Reference Levels in pediatric interventional cardiology: A multicenter study by the French cohort in HARMONIC projectBouchra Habib Geryes, Soline Bondet De La Bernardie, Sébastien Hascoet, et al.
Pediatric Cardiology|August 23, 2025
What Makes an Effective Chief of Pediatric Cardiology: Insights from Chiefs of Programs GloballyMichael E Kim, Lars Idorn, Sandra S Mattos, et al.
Archives of Disease in Childhood|November 13, 2025
Cause of death in children with heart disease: a cohort studyNeil Derridj, Daphné Madec, Olivier Raisky, et al.
ESC Heart Failure|March 10, 2020
Efficacy of phosphodiesterase type 5 inhibitors in univentricular congenital heart disease: the SV-INHIBITION study designPascal Amedro, Arthur Gavotto, Hamouda Abassi, et al.
Blood|June 12, 2004
Human blood IgM "memory" B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoireSandra Weller, Moritz C Braun, Bruce K Tan, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 11, 2025
Late outcomes of congenital and childhood non-immune, isolated atrioventricular block: a French nationwide retrospective cohort studyFlorence Mycinski, Victor Waldmann, Florence Kyndt, et al.
Circulation. Cardiovascular Genetics|December 9, 2015
Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the AortaMarta Sanchez-Castro, Hadja Eldjouzi, Eric Charpentier, et al.
Pediatric Research|December 8, 2010
Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 yearChantal Stheneur, Laurence Faivre, Gwenaëlle Collod-Béroud, et al.
Nature Genetics|August 5, 2008
ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulationCarine Le Goff, Fanny Morice-Picard, Nathalie Dagoneau, et al.
The European Respiratory Journal|December 11, 2025
Pulmonary hypertension in patients with Noonan syndromeJulien Grynblat, Mathieu Farges, Pascal Magro, et al.
Pageof 47

Showing results (391-400 of 461) with videos related to

Sort By:
Pageof 47
Plos One|September 17, 2025
Diagnostic Reference Levels in pediatric interventional cardiology: A multicenter study by the French cohort in HARMONIC projectBouchra Habib Geryes, Soline Bondet De La Bernardie, Sébastien Hascoet, et al.
Pediatric Cardiology|August 23, 2025
What Makes an Effective Chief of Pediatric Cardiology: Insights from Chiefs of Programs GloballyMichael E Kim, Lars Idorn, Sandra S Mattos, et al.
Archives of Disease in Childhood|November 13, 2025
Cause of death in children with heart disease: a cohort studyNeil Derridj, Daphné Madec, Olivier Raisky, et al.
ESC Heart Failure|March 10, 2020
Efficacy of phosphodiesterase type 5 inhibitors in univentricular congenital heart disease: the SV-INHIBITION study designPascal Amedro, Arthur Gavotto, Hamouda Abassi, et al.
Blood|June 12, 2004
Human blood IgM "memory" B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoireSandra Weller, Moritz C Braun, Bruce K Tan, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 11, 2025
Late outcomes of congenital and childhood non-immune, isolated atrioventricular block: a French nationwide retrospective cohort studyFlorence Mycinski, Victor Waldmann, Florence Kyndt, et al.
Circulation. Cardiovascular Genetics|December 9, 2015
Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the AortaMarta Sanchez-Castro, Hadja Eldjouzi, Eric Charpentier, et al.
Pediatric Research|December 8, 2010
Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 yearChantal Stheneur, Laurence Faivre, Gwenaëlle Collod-Béroud, et al.
Nature Genetics|August 5, 2008
ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulationCarine Le Goff, Fanny Morice-Picard, Nathalie Dagoneau, et al.
The European Respiratory Journal|December 11, 2025
Pulmonary hypertension in patients with Noonan syndromeJulien Grynblat, Mathieu Farges, Pascal Magro, et al.
Pageof 47