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Guy Vaksmann

Showing results (21-30 of 33) with videos related to

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Journal of Personalized Medicine|July 2, 2021
A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic ResponseMalorie Blancard, Zahia Touat-Hamici, Yuriana Aguilar-Sanchez, et al.
European Journal of Human Genetics : EJHG|December 16, 2018
Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variantsClémence Vanlerberghe, Anne-Sophie Jourdain, Jamal Ghoumid, et al.
Cardiology in the Young|June 17, 2014
ELN gene triplication responsible for familial supravalvular aortic aneurysmAnne-Sophie Guemann, Joris Andrieux, Florence Petit, et al.
Archives of Cardiovascular Diseases|May 31, 2024
Evaluation of new predictive scores for sudden cardiac death in childhood hypertrophic cardiomyopathy in a French cohortPierre-Alexandre Fontanges, Christelle Marquie, Ali Houeijeh, 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.
Respiratory Medicine and Research|May 11, 2026
The preponderance of genetic variations in paediatric pulmonary hypertensionJulien Grynblat, Mélanie Eyries, Marine Ambar-Akkaoui, et al.
European Journal of Cardiovascular Nursing|August 12, 2025
Health-Reported Quality of Life in Patients with A Systemic Right Ventricle: The QUALISYSTEMIC StudyPaul Padovani, Oscar Werner, Helena Huguet, et al.
American Journal of Human Genetics|June 5, 2013
Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosisJohn A Martignetti, Lifeng Tian, Dong Li, et al.
Archives of Cardiovascular Diseases|May 8, 2025
Anatomical insights and management strategies for haemodynamically significant pressure-restrictive perimembranous ventricular septal defects: Findings from the French nationwide FRANCISCO cohortAnnabel Sudaka, Jean-Benoit Thambo, Guy Vaksmann, et al.
Journal of Medical Genetics|June 25, 2025
Shprintzen-Goldberg syndrome: follow-up of the cardiovascular features in an international cohort of 29 patients with SGSYordi-Michaël Bouhatous, Pauline Arnaud, Guillaume Jondeau, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Journal of Personalized Medicine|July 2, 2021
A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic ResponseMalorie Blancard, Zahia Touat-Hamici, Yuriana Aguilar-Sanchez, et al.
European Journal of Human Genetics : EJHG|December 16, 2018
Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variantsClémence Vanlerberghe, Anne-Sophie Jourdain, Jamal Ghoumid, et al.
Cardiology in the Young|June 17, 2014
ELN gene triplication responsible for familial supravalvular aortic aneurysmAnne-Sophie Guemann, Joris Andrieux, Florence Petit, et al.
Archives of Cardiovascular Diseases|May 31, 2024
Evaluation of new predictive scores for sudden cardiac death in childhood hypertrophic cardiomyopathy in a French cohortPierre-Alexandre Fontanges, Christelle Marquie, Ali Houeijeh, 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.
Respiratory Medicine and Research|May 11, 2026
The preponderance of genetic variations in paediatric pulmonary hypertensionJulien Grynblat, Mélanie Eyries, Marine Ambar-Akkaoui, et al.
European Journal of Cardiovascular Nursing|August 12, 2025
Health-Reported Quality of Life in Patients with A Systemic Right Ventricle: The QUALISYSTEMIC StudyPaul Padovani, Oscar Werner, Helena Huguet, et al.
American Journal of Human Genetics|June 5, 2013
Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosisJohn A Martignetti, Lifeng Tian, Dong Li, et al.
Archives of Cardiovascular Diseases|May 8, 2025
Anatomical insights and management strategies for haemodynamically significant pressure-restrictive perimembranous ventricular septal defects: Findings from the French nationwide FRANCISCO cohortAnnabel Sudaka, Jean-Benoit Thambo, Guy Vaksmann, et al.
Journal of Medical Genetics|June 25, 2025
Shprintzen-Goldberg syndrome: follow-up of the cardiovascular features in an international cohort of 29 patients with SGSYordi-Michaël Bouhatous, Pauline Arnaud, Guillaume Jondeau, et al.
Pageof 4