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Archives of Cardiovascular Diseases
|
November 19, 2019
Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndrome
Sebastien 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 rate
Maya 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 syndrome
Antoine 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 study
Alban-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 dissections
Mathieu Barbier, Marie-Sylvie Gross, Mélodie Aubart, et al.
European Heart Journal
|
May 4, 2015
Marfan Sartan: a randomized, double-blind, placebo-controlled trial
Olivier 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 block
Alban-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 Trial
Johan Moreau, Caroline Neyraud, Helena Huguet, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 88) with videos related to
Sort By:
Page
of 9
Archives of Cardiovascular Diseases
|
November 19, 2019
Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndrome
Sebastien 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 rate
Maya 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 syndrome
Antoine 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 study
Alban-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 dissections
Mathieu Barbier, Marie-Sylvie Gross, Mélodie Aubart, et al.
European Heart Journal
|
May 4, 2015
Marfan Sartan: a randomized, double-blind, placebo-controlled trial
Olivier 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 block
Alban-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 Trial
Johan Moreau, Caroline Neyraud, Helena Huguet, et al.
Page
of 9