Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Yves Dulac

Showing results (71-80 of 88) with videos related to

Pageof 9
Sort By:
Archives of Cardiovascular Diseases|November 19, 2019
Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndromeSebastien Hascoet, Thomas Edouard, Julie Plaisancie, et al.
Archives of Cardiovascular Diseases|March 12, 2022
Radiation dose during catheter ablation in children using a low fluoroscopy frame rateMaya Riche, Sylvie Monfraix, Sebastien Balduyck, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 12, 2019
Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD)Pauline Arnaud, Nadine Hanna, Louise Benarroch, et al.
Heart Rhythm|February 28, 2016
Impact of clinical and genetic findings on the management of young patients with Brugada syndromeAntoine Andorin, Elijah R Behr, Isabelle Denjoy, et al.
European Heart Journal|September 17, 2011
Characteristics and long-term outcome of non-immune isolated atrioventricular block diagnosed in utero or early childhood: a multicentre studyAlban-Elouen Baruteau, Swanny Fouchard, Albin Behaghel, et al.
American Journal of Human Genetics|December 1, 2014
MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissectionsMathieu Barbier, Marie-Sylvie Gross, Mélodie Aubart, et al.
European Heart Journal|May 4, 2015
Marfan Sartan: a randomized, double-blind, placebo-controlled trialOlivier Milleron, Florence Arnoult, Jacques Ropers, et al.
Circulation|August 18, 2012
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular blockAlban-Elouen Baruteau, Albin Behaghel, Swanny Fouchard, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 29, 2006
[Recommendations for the medical management of aortic complications of Marfan's syndrome]Guillaume Jondeau, Martine Barthelet, Clarisse Baumann, et al.
European Journal of Cardiovascular Nursing|April 29, 2026
Remote Sophrology in Congenital Heart Disease: The SOPHROCARE Randomized Controlled TrialJohan Moreau, Caroline Neyraud, Helena Huguet, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
Archives of Cardiovascular Diseases|November 19, 2019
Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndromeSebastien Hascoet, Thomas Edouard, Julie Plaisancie, et al.
Archives of Cardiovascular Diseases|March 12, 2022
Radiation dose during catheter ablation in children using a low fluoroscopy frame rateMaya Riche, Sylvie Monfraix, Sebastien Balduyck, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 12, 2019
Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD)Pauline Arnaud, Nadine Hanna, Louise Benarroch, et al.
Heart Rhythm|February 28, 2016
Impact of clinical and genetic findings on the management of young patients with Brugada syndromeAntoine Andorin, Elijah R Behr, Isabelle Denjoy, et al.
European Heart Journal|September 17, 2011
Characteristics and long-term outcome of non-immune isolated atrioventricular block diagnosed in utero or early childhood: a multicentre studyAlban-Elouen Baruteau, Swanny Fouchard, Albin Behaghel, et al.
American Journal of Human Genetics|December 1, 2014
MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissectionsMathieu Barbier, Marie-Sylvie Gross, Mélodie Aubart, et al.
European Heart Journal|May 4, 2015
Marfan Sartan: a randomized, double-blind, placebo-controlled trialOlivier Milleron, Florence Arnoult, Jacques Ropers, et al.
Circulation|August 18, 2012
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular blockAlban-Elouen Baruteau, Albin Behaghel, Swanny Fouchard, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 29, 2006
[Recommendations for the medical management of aortic complications of Marfan's syndrome]Guillaume Jondeau, Martine Barthelet, Clarisse Baumann, et al.
European Journal of Cardiovascular Nursing|April 29, 2026
Remote Sophrology in Congenital Heart Disease: The SOPHROCARE Randomized Controlled TrialJohan Moreau, Caroline Neyraud, Helena Huguet, et al.
Pageof 9