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Neuromuscular Disorders : NMD|December 19, 2021
Kennedy disease in two sisters with biallelic CAG expansions of the androgen receptor geneKai Ivar Müller, Øivind Nilssen, Maria Nebuchenykh, et al.
Neuromuscular Disorders : NMD|December 17, 2021
Alanine transaminase is predominantly increased in the active phase of anti-HMGCR myopathyAkatsuki Kubota, Jun Shimizu, Atsushi Unuma, et al.
Neuromuscular Disorders : NMD|January 4, 2022
Novel pathogenic ALG2 mutation causing congenital myasthenic syndrome: A case reportChristoffer Ehrstedt, Wei-Wei Liu, Carina Frykholm, et al.
Neuromuscular Disorders : NMD|March 9, 2021
Importance of immunohistochemical evaluation of developmentally regulated myosin heavy chains in human muscle biopsiesC A Sewry, L Feng, D Chambers, et al.
Neuromuscular Disorders : NMD|November 5, 2021
Primary mitochondrial myopathies in childhoodCatarina Olimpio, May Yung Tiet, Rita Horvath
Neuromuscular Disorders : NMD|October 21, 2022
Long term noninvasive ventilation and continuous positive airway pressure in children with neuromuscular diseases in FranceLaura Allaer, Sonia Khirani, Lucie Griffon, et al.
Neuromuscular Disorders : NMD|November 2, 2022
Muscle ultrasound in hereditary muscle diseaseAndrew Hannaford, Steve Vucic, Nens van Alfen, et al.
Neuromuscular Disorders : NMD|October 24, 2022
TEMPORARY REMOVAL: VP.47 Interleukin 31 (IL-31) inhibition as a trigger for an immune-mediated myopathy?M Winkler, K Kappes-Horn, J Reimann
Neuromuscular Disorders : NMD|October 7, 2022
Masseter muscle volume as a disease marker in adult-onset myotonic dystrophy type 1Agata Oliwa, Clarissa Hocking, Mark J Hamilton, et al.
Neuromuscular Disorders : NMD|October 3, 2022
Having an eye for myotonic dystrophy: A qualitative study on experiences and support needs in myotonic dystrophy type 1 patients with a diagnostic delay after early-onset cataractI E A Karnebeek, H T M Boon, A M P Huis, et al.
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