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Neuromuscular Disorders : NMD|April 25, 2015
Role of the cardio-pulmonary exercise test and six-minute walking test in the evaluation of exercise performance in patients with late-onset Pompe diseaseG Crescimanno, R Modica, R Lo Mauro, et al.
Neuromuscular Disorders : NMD|April 23, 2015
Phenotypic variability of TRPV4 related neuropathiesTeresinha Evangelista, Boglarka Bansagi, Angela Pyle, et al.
Neuromuscular Disorders : NMD|February 3, 1998
A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase lociN B Romero, D Récan, O Rigal, et al.
Neuromuscular Disorders : NMD|February 3, 1998
On a dominantly inherited myopathy with tubular aggregatesJ J Martin, C Ceuterick, G Van Goethem
Neuromuscular Disorders : NMD|July 1, 1997
Problems and potential for gene therapy in Duchenne muscular dystrophyB A Kakulas
Neuromuscular Disorders : NMD|April 21, 2015
Respiratory failure as presenting symptom of necrotizing autoimmune myopathy with anti-melanoma differentiation-associated gene 5 antibodiesBregje Jaeger, Marianne de Visser, Eleonora Aronica, et al.
Neuromuscular Disorders : NMD|April 7, 2021
Motor unit number index (MUNIX) in children and adults with 5q-spinal muscular atrophy: Variability and clinical correlationsRodrigo Holanda Mendonça, Ligia Maria Sotero Machado, Carlos Otto Heise, et al.
Neuromuscular Disorders : NMD|July 15, 2020
An unusual case of recurrent episodes of muscle weakness: Co-occurrence of Andersen-Tawil syndrome and glycogen storage disease type IXdHonghao Li, Yuan Xue, Jing Yu, et al.
Neuromuscular Disorders : NMD|July 22, 2020
Utility of maximum inspiratory and expiratory pressures as a screening method for respiratory insufficiency in slowly progressive neuromuscular disordersStephan Wenninger, Kristina Stahl, Corinna Wirner, et al.
Neuromuscular Disorders : NMD|May 19, 2023
Safety, tolerability and pharmacokinetics of eteplirsen in young boys aged 6-48 months with Duchenne muscular dystrophy amenable to exon 51 skippingE Mercuri, A M Seferian, L Servais, et al.
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