Neuromuscular Disorders Volume 40 p1-52 (July 2024) Todas las revistas Ir al última publicación Office-based respiratory assessment in patients with generalized myasthenia gravis Monica Alcantara,Carolina Barnett-Tapia,Vera Bril,...Eduardo Ng,Clodagh Ryan,Hans Katzberg Further expanding the phenotype of anti-Ku antibody associated disease in children and adolescents Ezgi Deniz Batu,Seher Sener,Göknur Haliloglu, Diclehan Orhan,Üstün Aydingöz, Seza Özen Main features and disease outcome of congenital myotonic dystrophy - experience from a single tertiary center Slavica Ostojic, Gordana Kovacevic, Giovanni Meola,...Katarina Pejic, Snežana Ristic, Stojan Peric Resistance training in women with myotonic dystrophy type 1: a multisystemic therapeutic avenue Laura Girard-Côté, Benjamin Gallais, Cynthia Gagnon,...Gilles Gouspillou, Vincent Marcangeli, Elise Duchesne Different neuropsychological and brain volumetric profiles in a pair of identical twins with myotonic dystrophy type 1 indicate a non-genetic modulation of clinical phenotype Laura Serra, Antonio Petrucci, Michela Bruschini,...Corrado Campisi, Carlo Caltagirone, Marco Bozzali Severe gastrointestinal problems in Duchenne muscular dystrophy: A case series AM Blokhuis, KMAJ Tytgat, JT Groothuis, SLS Houwen-van Opstal Ver seleccionados