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Neuromuscular Disorders : NMD|October 19, 2020
Insulin-like growth factor-1 status is associated with insulin resistance in young patients with spinal muscular atrophyAvivit Brener, Liora Sagi, Anna Shtamler, et al.Neuromuscular Disorders : NMD|October 19, 2020
Adalimumab and myositis: A case report and review of the French and international Pharmacovigilance DatabasesLouise Gaboriau, Jean-Baptiste Davion, Sandrine Combret, et al.Neuromuscular Disorders : NMD|December 17, 2018
The oral splicing modifier RG7800 increases full length survival of motor neuron 2 mRNA and survival of motor neuron protein: Results from trials in healthy adults and patients with spinal muscular atrophyHeidemarie Kletzl, Anne Marquet, Andreas Günther, et al.Neuromuscular Disorders : NMD|December 17, 2018
Autophagic vacuolar myopathy caused by a CLN3 mutation. A case reportFrancesca Moro, Anna Rubegni, Francesca Pochiero, et al.Neuromuscular Disorders : NMD|December 3, 2019
GNE myopathy - A cross-sectional study on spatio-temporal gait characteristicsGaurav Gomez, Meeka Khanna, Anupam Gupta, et al.Neuromuscular Disorders : NMD|November 28, 2020
Long-term follow-up of patients with type 2 and non-ambulant type 3 spinal muscular atrophy (SMA) treated with olesoxime in the OLEOS trialFrancesco Muntoni, Enrico Bertini, Giacomo Comi, et al.Neuromuscular Disorders : NMD|October 31, 2020
Respiratory muscle training in late-onset Pompe disease: Results of a sham-controlled clinical trialHarrison N Jones, Maragatha Kuchibhatla, Kelly D Crisp, et al.Neuromuscular Disorders : NMD|April 9, 2022
Frontal lobe-dominant cerebral blood flow reduction and atrophy can be progressive in Duchenne muscular dystrophyMadoka Mori-Yoshimura, Kazutaka Aizawa, Yoko Shigemoto, et al.Neuromuscular Disorders : NMD|April 9, 2022
Real-world and natural history data for drug evaluation in Duchenne muscular dystrophy: suitability of the North Star Ambulatory Assessment for comparisons with external controlsFrancesco Muntoni, James Signorovitch, Gautam Sajeev, et al.Neuromuscular Disorders : NMD|July 28, 2022
Assessment of the upper limb muscles in patients with Fukuyama muscular dystrophy: Noninvasive assessment using visual ultrasound muscle analysis and shear wave elastographyRisa Harada, Mariko Taniguchi-Ikeda, Miwako Nagasaka, et al.Pageof 341