Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Pascal Amédro"'
Autor:
Gregoire De La Villeon, Arthur Gavotto, Nam Ledong, Charlene Bredy, Sophie Guillaumont, Jonathan Man, Fares Gouzi, Maurice Hayot, Thibault Mura, Pascal Amedro, Stefan Matecki
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 8, Iss , Pp 100346- (2022)
Aim: Exercise capacity is altered in congenital heart diseases (CHD) with potentially impaired pulmonary perfusion adaptation during exercise, such as in single ventricle or in significant pulmonary regurgitation. This study aimed to evaluate the val
Externí odkaz:
https://doaj.org/article/e2e859df022944ad9bc9a3eb55d7a086
Autor:
Monia Souidi, Jessica Resta, Haikel Dridi, Yvonne Sleiman, Steve Reiken, Karina Formoso, Sarah Colombani, Pascal Amédro, Pierre Meyer, Azzouz Charrabi, Marie Vincenti, Yang Liu, Rajesh Kumar Soni, Frank Lezoualc'h, D.V.M. Stéphane Blot, François Rivier, Olivier Cazorla, Angelo Parini, Andrew R. Marks, Jeanne Mialet‐Perez, Alain Lacampagne, Albano C. Meli
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 15, Iss 2, Pp 536-551 (2024)
Abstract Background Duchenne muscular dystrophy (DMD) is an X‐linked disorder characterized by progressive muscle weakness due to the absence of functional dystrophin. DMD patients also develop dilated cardiomyopathy (DCM). We have previously shown
Externí odkaz:
https://doaj.org/article/86cf946208c7405482fdfb4f8454571b
Autor:
Lamia Goual, Elisa Bounasri, Marie Vincenti, Pascal Amédro, Romain Desprat, Florence Bernex, Jean-Marc Lemaitre, Jean-Luc Pasquié, Alain Lacampagne, Jérôme Thireau, Albano C. Meli
Publikováno v:
Stem Cell Research, Vol 72, Iss , Pp 103192- (2023)
Type 2 Long QT Syndrome (LQT2) is a rare genetic heart rhythm disorder causing life-threatening arrhythmias. We derived induced pluripotent stem cell (iPSC) lines from two patients with LQT2, aged 18 and 6, both carrying a heterozygous missense mutat
Externí odkaz:
https://doaj.org/article/16c770daa94b42f79ad7aa71345f5a15
Autor:
Sarah Colombani, Albin A. Bernardin, Marie Vincenti, Pascal Amédro, Romain Desprat, Florence Bernex, Jean-Marc Lemaitre, Jean-Luc Pasquié, Alain Lacampagne, Albano C. Meli
Publikováno v:
Stem Cell Research, Vol 60, Iss , Pp 102727- (2022)
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) is a genetic disorder characterized by ventricular tachycardia, that can cause the heart to stop beating leading to death. The prevalence is 1/10.000 and in approximately 60% of cases, the
Externí odkaz:
https://doaj.org/article/0e799d59ef3a4cc287ab84150a14e068
Autor:
Monia Souidi, Pascal Amédro, Pierre Meyer, Romain Desprat, Jean-Marc Lemaître, François Rivier, Alain Lacampagne, Albano C. Meli
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102094- (2020)
Duchenne Muscular Dystrophy (DMD) is a X-linked degenerative pathology with a prevalence of 1/3600–6000 boys due to the absence of functional dystrophin in muscles. This muscular disease leads to skeletal muscle damages, respiratory failure and in
Externí odkaz:
https://doaj.org/article/e27431ff0bcd438bbf860c396382d7e4
Cardiac rehabilitation in children and adolescents with long QT syndrome: the RYTHMO’FIT pilot study
Autor:
Luc Souilla, Sophie Guillaumont, Annie Auer, Gael Metzler, Anne Requirand, Marie Vincenti, Gregoire De La Villeon, Jean-Luc Pasquie, Denis Mottet, Pascal Amedro
Publikováno v:
BMC Sports Science, Medicine and Rehabilitation, Vol 16, Iss 1, Pp 1-13 (2024)
Abstract Background To assess the feasibility, acceptability, safety, and short-term benefits of a tailored cardiac rehabilitation program for children and adolescents with long QT syndrome (LQTS). Methods Eight participants, aged between 6 and 18, w
Externí odkaz:
https://doaj.org/article/f4be3ce2a29545c1adef46c77b626f39
Autor:
Thomas Edouard, Marie-Christine Picot, Fernanda Bajanca, Helena Huguet, Aitor Guitarte, Maud Langeois, Bertrand Chesneau, Philippe Khau Van Kien, Eric Garrigue, Yves Dulac, Pascal Amedro
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background This cross-sectional controlled study aims to assess health-related quality of life (HRQoL) of children and adolescents with a molecular diagnosis of Marfan syndrome (MFS) or related disorders and to evaluate the factors associate
Externí odkaz:
https://doaj.org/article/3fdcf20d63e3405d901d1338b04c6ed7
Autor:
Pascal Amedro, Stefan Matecki, Taissa Pereira dos Santos, Sophie Guillaumont, Jonathan Rhodes, Suellen Moli Yin, Alfred Hager, Julia Hock, Gregoire De La Villeon, Johan Moreau, Anne Requirand, Luc Souilla, Marie Vincenti, Marie-Christine Picot, Helena Huguet, Thibault Mura, Arthur Gavotto
Publikováno v:
Sports Medicine - Open, Vol 9, Iss 1, Pp 1-12 (2023)
Abstract Background The evaluation of health status by cardiopulmonary exercise test (CPET) has shown increasing interest in the paediatric population. Our group recently established reference Z-score values for paediatric cycle ergometer VO2max, app
Externí odkaz:
https://doaj.org/article/0c69d83531254c12b380ab0bf153c985
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background We report the occurrence of a severe pulmonary hypertension (PH) in a neonate affected by a left congenital diaphragmatic hernia (CDH). PH in this patient was associated with an abnormal origin of the right pulmonary artery from t
Externí odkaz:
https://doaj.org/article/2ee0ec60df3a4633887d93ee0a02c754
Autor:
Reaksmei Ly, Clément Karsenty, Pascal Amedro, Sarah Cohen, Olivia Domanski, Francois Godart, Jelena Radojevic, Guy Vaksmann, Nicole Naccache, Anissa Boubrit, Vincent Bataille, Sébastien Hascoet, Magalie Ladouceur
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 8 (2023)
Background Quality of Life (QoL) is a prognostic factor in heart failure (HF) of patients with acquired cardiac disease. The aim of this study was to determine the predictive value of QoL on outcomes in adults with congenital heart disease (ACHD) and
Externí odkaz:
https://doaj.org/article/f5297bbb897b400485abbcf2b022da37