Neuromuscular Disorders Volume 42 p 1-52 (September 2024) Todas las revistas Granulomatous myositis: characteristics and outcome from a monocentric retrospective cohort study Hippolyte Lequain,Nathalie Streichenberger,Laure Gallay,...Yvan Jamilloux,Pascal Leblanc,Pascal Sève Improving Heckmatt muscle ultrasound grading scale through Rasch analysis Juerd Wijntjes, Christiaan Saris, Jonne Doorduin, Nens van Alfen, Baziel van Engelen, Karlien Mul Population-based incidence rates of 15 neuromuscular disorders: a nationwide capture-recapture study in the Netherlands Johanna C.W. Deenen,Corinne G.C. Horlings,Nicol C. Voermans,...Jan J.G.M. Verschuuren,André L.M. Verbeek,Baziel G.M. van Engelen Defining the landscape of TIA1 and SQSTM1 digenic myopathy Paula Panos-Basterra,Julian Theuriet,Aleksandra Nadaj-Pakleza,...Antoine Pegat,Tanya Stojkovic,Gorka Fernández-Eulate Ophthalmoparesis as an unusual manifestation of anti-3-hydroxy-3-methyl-glutaryl-coenzyme A reductase antibody-associated myopathies Brendan Putko,Alan Pestronk,Gregory P. Van Stavern,Cecile L. Phan,Grayson Beecher,Teerin Liewluck Risk-benefit profile of onasemnogene abeparvovec in older and heavier children with spinal muscular atrophy type 1 Rebecca Finnegan,Adnan Manzur,Pinki Munot,...Giovanni Baranello,Francesco Muntoni,Mariacristina Scoto Three novel missense variants in two families with JAG2-associated limb-girdle muscular dystrophy Lein Dofash,Krishnan Lyengar,Nolette Pereira,...Matthew Lynch,Mark Davis,Gianina Ravenscroft Ver seleccionados