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Muscle & Nerve|March 27, 2015
Whole-body muscle magnetic resonance imaging in SEPN1-related myopathy shows a homogeneous and recognizable patternKarolina Hankiewicz, Robert Y Carlier, Leila Lazaro, et al.European Heart Journal|July 31, 2015
Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseasesKarim Wahbi, Wulfran Bougouin, Anthony Béhin, et al.JAMA Neurology|February 8, 2021
Comparison of Corticosteroid Tapering Regimens in Myasthenia Gravis: A Randomized Clinical TrialTarek Sharshar, Raphaël Porcher, Sophie Demeret, et al.Neuromuscular Disorders : NMD|July 13, 2010
Investigating glycogenosis type III patients with multi-parametric functional NMR imaging and spectroscopyClaire Wary, Aleksandra Nadaj-Pakleza, Pascal Laforêt, et al.Journal of Inherited Metabolic Disease|October 26, 2019
Incidence and predictors of total mortality in 267 adults presenting with mitochondrial diseasesConstantinos Papadopoulos, Karim Wahbi, Anthony Behin, et al.Brain : a Journal of Neurology|February 4, 2006
Shared blood and muscle CD8+ T-cell expansions in inclusion body myositisDalia Dimitri, Olivier Benveniste, Odile Dubourg, et al.Journal of Inherited Metabolic Disease|November 26, 2019
A high prevalence of arterial hypertension in patients with mitochondrial diseasesCaroline Chong-Nguyen, Caroline Stalens, Yves Goursot, et al.Neuromuscular Disorders : NMD|January 24, 2015
Abnormal sodium current properties contribute to cardiac electrical and contractile dysfunction in a mouse model of myotonic dystrophy type 1Vincent Algalarrondo, Karim Wahbi, Frédéric Sebag, et al.The American Journal of Pathology|April 17, 2010
DNAJB2 expression in normal and diseased human and mouse skeletal muscleKristl G Claeys, Magdalena Sozanska, Jean-Jacques Martin, et al.Annals of Clinical and Translational Neurology|April 16, 2016
Natural history of LGMD2A for delineating outcome measures in clinical trialsIsabelle Richard, Jean-Yves Hogrel, Daniel Stockholm, et al.Pageof 26