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Neuromuscular Disorders : NMD|October 27, 2019
Fatigue in primary genetic mitochondrial disease: No rest for the wearySumit Parikh, Rachel Galioto, Brittany Lapin, et al.
Neuromuscular Disorders : NMD|April 16, 2020
Beyond ambulation: Measuring physical activity in youth with Duchenne muscular dystrophyMary Killian, Maciej S Buchowski, Thomas Donnelly, et al.
Neuromuscular Disorders : NMD|May 4, 2020
Severe congenital myasthenic syndrome associated with novel biallelic mutation of the CHRND geneCarmen Bonanno, Carmelo Rodolico, Ana Töpf, et al.
Neuromuscular Disorders : NMD|April 22, 2020
The Association of methylprednisolone dosing to cessation of myotonia in a patient with myotonic dystrophy type 1Magda Horáková, Tomáš Horák, Josef Bednařík, et al.
Neuromuscular Disorders : NMD|April 19, 2020
No effect of oral sucrose or IV glucose during exercise in phosphorylase b kinase deficiencyA G Andersen, M C Ørngreen, D E T Raaschou-Pedersen, et al.
Neuromuscular Disorders : NMD|August 29, 2021
Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variantsYun Jeong Lee, Soo Yeon Kim, Man Jin Kim, et al.
Neuromuscular Disorders : NMD|October 21, 2019
Longitudinal natural history in young boys with Duchenne muscular dystrophyGiorgia Coratti, Claudia Brogna, Giulia Norcia, et al.
Neuromuscular Disorders : NMD|July 20, 2015
Hereditary neuropathy with liability to pressure palsies in childhood: Case series and literature updateNicolas Chrestian, Hugh McMillan, Chantal Poulin, et al.
Neuromuscular Disorders : NMD|September 4, 2025
An observational longitudinal study of congenital myasthenic syndromesHayley Ramjattan, Leighann Henehan, Sithara Ramdas, et al.
Neuromuscular Disorders : NMD|June 2, 2015
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature reviewPaolo Emilio Alboini, Valentina Damato, Raffaele Iorio, et al.
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