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Neuromuscular Disorders : NMD|November 13, 2018
Isokinetic assessment of trunk muscles in facioscapulohumeral muscular dystrophy type 1 patientsJulien Esnault, Besma Missaoui, Samy Bendaya, et al.
Neurogenetics|December 4, 2003
New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian familiesNacim Louhichi, Chahnez Triki, Susana Quijano-Roy, et al.
Annals of Neurology|December 21, 2005
SEPN1: associated with congenital fiber-type disproportion and insulin resistanceNigel F Clarke, Warren Kidson, Susana Quijano-Roy, et al.
Brain : a Journal of Neurology|June 22, 2014
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophySophie Nicole, Amina Chaouch, Torberg Torbergsen, et al.
Annals of Neurology|September 25, 2004
Electromyography guides toward subgroups of mutations in muscle channelopathiesEmmanuel Fournier, Marianne Arzel, Damien Sternberg, et al.
Neuromuscular Disorders : NMD|April 9, 2008
Left ventricular non-compaction in a patient with myotonic dystrophy type 2Karim Wahbi, Christophe Meune, Guillaume Bassez, et al.
Neuromuscular Disorders : NMD|June 14, 2017
Diaphragmatic dysfunction in SEPN1-related myopathySerena Caggiano, Sonia Khirani, Ivana Dabaj, et al.
Medicine|January 26, 2019
Assessment of diaphragm motion using ultrasonography in a patient with facio-scapulo-humeral dystrophy: A case reportAbdallah Fayssoil, Tanya Stojkovic, Adam Ogna, et al.
Frontiers in Immunology|May 22, 2020
Comparative Analysis of Thymic and Blood Treg in Myasthenia Gravis: Thymic Epithelial Cells Contribute to Thymic Immunoregulatory DefectsFrédérique Truffault, Dani Nazzal, Julien Verdier, et al.
Annals of Neurology|January 27, 2006
Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravisClaire Vandiedonck, Claire Capdevielle, Matthieu Giraud, et al.
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