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Neuromuscular Disorders : NMD|August 18, 2026
Identification of a novel likely pathogenic MT-TS2 variant in a patient with mitochondrial myopathy, retinitis pigmentosa and sensorineural hearing lossMadalena Couto, Mafalda Delgado Soares, Pedro Coelho, et al.
Neuromuscular Disorders : NMD|September 8, 2026
Integrating EMG and plasma biomarkers to characterize neuromuscular remodeling in sarcopeniaRizwan Qaisar, Mashal Javed, Imran Muhammad Khan, et al.
Neuromuscular Disorders : NMD|September 11, 2026
Noninfectious meningitis related to nusinersen: a pharmacovigilance analysis using the WHO databaseLeonie Kriz, Bettina Schreiner, Veronika Kana, et al.
Neuromuscular Disorders : NMD|September 11, 2026
Congenital myasthenic syndromes in Türkiye: genetic and clinical spectrum revisited in a nationwide pediatric cohortCanan Üstün, İpek Polat, Gülten Öztürk, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Nitric oxide: biologic effects on muscle and role in muscle diseasesH J Kaminski, F H Andrade
Neuromuscular Disorders : NMD|August 30, 2001
Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophyK M Flanigan, C M Coffeen, L Sexton, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Identification and functional characterization of a novel ryanodine receptor mutation causing malignant hyperthermia in North American and South American familiesN Sambuughin, T E Nelson, J Jankovic, et al.
Neuromuscular Disorders : NMD|August 30, 2001
A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction blockT Kitaguchi, S Matsubara, M Sato, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Respiratory chain defects in hereditary spastic paraplegiasF Piemonte, C Casali, R Carrozzo, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Merosin-positive congenital muscular dystrophy with mental retardation, microcephaly and central nervous system abnormalities unlinked to the Fukuyama muscular dystrophy and muscular-eye-brain loci: report of three siblingsV Ruggieri, F Lubieniecki, F Meli, et al.
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