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Journal of Neuromuscular Diseases|December 28, 2017
Diaphragm: Pathophysiology and Ultrasound Imaging in Neuromuscular DisordersAbdallah Fayssoil, Anthony Behin, Adam Ogna, et al.Circulation. Cardiovascular Genetics|June 15, 2017
Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart RegistryCaroline Chong-Nguyen, Karim Wahbi, Vincent Algalarrondo, et al.Nature|August 10, 2007
An IRF8-binding promoter variant and AIRE control CHRNA1 promiscuous expression in thymusMatthieu Giraud, Richard Taubert, Claire Vandiedonck, et al.Muscle & Nerve|February 7, 2017
The quality of life in genetic neuromuscular disease questionnaire: Rasch validation of the French versionAntoine Dany, Amandine Rapin, Brice Lavrard, et al.Genetic Testing and Molecular Biomarkers|June 21, 2018
Genetic Mutations and Demographic, Clinical, and Morphological Aspects of Myofibrillar Myopathy in a French CohortAlzira Alves de Siqueira Carvalho, Emmanuele Lacene, Guy Brochier, et al.Brain Communications|May 25, 2022
Unravelling the impact of frontal lobe impairment for social dysfunction in myotonic dystrophy type 1Alexandre Morin, Aurelie Funkiewiez, Alexandre Routier, et al.Human Mutation|January 16, 2007
Conspicuous involvement of desmin tail mutations in diverse cardiac and skeletal myopathiesHarald Bär, Bertrand Goudeau, Sarah Wälde, et al.Plos One|March 6, 2014
Th1 response and systemic treg deficiency in inclusion body myositisYves Allenbach, Wahiba Chaara, Michelle Rosenzwajg, et al.Scientific Reports|August 28, 2023
New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani-Lenz syndromeMarion Masingue, Olivia Cattaneo, Nicolas Wolff, et al.Plos One|April 25, 2019
Diaphragm sniff ultrasound: Normal values, relationship with sniff nasal pressure and accuracy for predicting respiratory involvement in patients with neuromuscular disordersAbdallah Fayssoil, Lee S Nguyen, Adam Ogna, et al.Pageof 21