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Journal of Neurology|July 9, 2023
Diagnosis and management of Becker muscular dystrophy: the French guidelinesArmelle Magot, Karim Wahbi, France Leturcq, et al.
International Journal of Cardiology|July 15, 2010
N-terminal Pro brain natriuretic peptide is a reliable biomarker of reduced myocardial contractility in patients with lamin A/C gene mutationsChristophe Meune, Karim Wahbi, Camille Gobeaux, et al.
Journal of Neuromuscular Diseases|September 29, 2019
The Added Value of Cardiac Magnetic Resonance in Muscular DystrophiesMariana M Lamacie, Jodi Warman-Chardon, Andrew M Crean, et al.
Archives of Cardiovascular Diseases|February 1, 2011
Combination of copeptin and high-sensitivity cardiac troponin T assay in unstable angina and non-ST-segment elevation myocardial infarction: a pilot studyChristophe Meune, Stéphane Zuily, Karim Wahbi, et al.
Journal of Inherited Metabolic Disease|December 28, 2020
Narrative review of glycogen storage disorder type III with a focus on neuromuscular, cardiac and therapeutic aspectsÉdouard Berling, Pascal Laforêt, Karim Wahbi, et al.
Neuromuscular Disorders : NMD|November 11, 2011
Blood glutathione decrease in subjects carrying lamin A/C gene mutations is an early marker of cardiac involvementChristophe Meune, Lara Khouzami, Karim Wahbi, et al.
Journal of Neuromuscular Diseases|March 8, 2021
Laminopathies' Treatments Systematic Review: A Contribution Towards a 'Treatabolome'Antonio Atalaia, Rabah Ben Yaou, Karim Wahbi, et al.
Pediatrics|August 4, 2010
Cardiac findings in congenital muscular dystrophiesJosef Finsterer, Claudio Ramaciotti, Ching H Wang, et al.
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