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Neuromuscular Disorders : NMD|May 21, 2024
Retrospective analysis of efgartigimod use in patients with double-seronegative generalized myasthenia gravis: a case seriesKazuhiro Horiuchi, Shuntaro Nakamura, Kazuki Yamada, et al.
Neuromuscular Disorders : NMD|April 16, 2024
Mycophenolate and methotrexate are better tolerated than azathioprine in myasthenia gravisKatherine C Dodd, Rohan Ahmed, Philip Ambrose, et al.
Neuromuscular Disorders : NMD|November 25, 2025
287th ENMC international workshop: Harmonization and federated analysis of myotonic dystrophy registries to model heterogeneous disease trajectories. Hoofddorp, the Netherlands, 28-30 March 2025Leandre A la Fontaine, Daniël van As, Guillaume Bassez, et al.
Neuromuscular Disorders : NMD|November 25, 2025
Mills' syndrome and myasthenia gravis: a case reportJonathan Morena, James Hiana, Ryan Naum, et al.
Neuromuscular Disorders : NMD|December 22, 2024
Desmoid tumour: a rare cause of congenital unilateral calf enlargement mimicking calf hypertrophyMaha Elseed, James N Sampson, Tuomo Polvikoski, et al.
Neuromuscular Disorders : NMD|February 5, 2025
Italian survey on evolving SMA care with disease-modifying therapies: a consensus workshop on nutrition, swallowing, respiratory and rehabilitation careStefania Corti, Valeria Sansone, Ilaria Bitetti, et al.
Neuromuscular Disorders : NMD|December 27, 2023
Cost-effectiveness of spinal muscular atrophy newborn screening based on real-world data in BelgiumTamara Dangouloff, Praveen Thokala, Matthew D Stevenson, et al.
Neuromuscular Disorders : NMD|December 29, 2023
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month studyGiorgia Coratti, Marika Pane, Claudia Brogna, et al.
Neuromuscular Disorders : NMD|December 27, 2023
Raised CK and acute kidney injury following intense exercise in three patients with a history of exercise intolerance due to homozygous mutations in SLC2A9Ros Quinlivan, Elaine Murphy, Shpresa Pula, et al.
Neuromuscular Disorders : NMD|December 13, 2023
Description of clinical and genetic features of 122 patients included in the Spanish Pompe registryRafael Jenaro Martinez-Marin, David Reyes-Leiva, Andrés Nascimento, et al.
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