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Neuromuscular Disorders : NMD|October 27, 2021
The impact of testosterone therapy on quality of life in adolescents with Duchenne muscular dystrophyC L Wood, J Page, J Foggin, et al.
Neuromuscular Disorders : NMD|July 4, 2019
The prevalence of faecal incontinence in myotonic dystrophy type 1R K H Petty, M P Eugenicos, M J Hamilton, et al.
Neuromuscular Disorders : NMD|June 16, 2019
Salbutamol tolerability and efficacy in patients with spinal muscular atrophy type IIA L Frongia, D Natera-de Benito, C Ortez, et al.
Neuromuscular Disorders : NMD|October 13, 2019
A novel case of inclusion body myositis and myasthenia gravisSakis Lambrianides, Evgenios Kinnis, Michele Cleanthous, et al.
Neuromuscular Disorders : NMD|March 27, 2022
Instrumental activities of daily living in adults with the DM1 childhood phenotype: going beyond motor impairmentsSamar Muslemani, Cynthia Gagnon, Benjamin Gallais
Neuromuscular Disorders : NMD|April 28, 2022
Bi-allelic MYH3 loss-of-function variants cause a lethal form of contractures, pterygia, and spondylocarpotarsal fusion syndrome 1BBenjamin Kamien, Joshua S Clayton, Han-Shin Lee, et al.
Neuromuscular Disorders : NMD|October 12, 2021
An autopsied case of ADSSL1 myopathyAtsuko Motoda, Tetsuya Takahashi, Chigusa Watanabe, et al.
Neuromuscular Disorders : NMD|January 31, 2022
Hypotonic infant with PURA syndrome-related channelopathy successfully treated with pyridostigmineRita Wyrebek, Mara DiBartolomeo, Sandra Brooks, et al.
Neuromuscular Disorders : NMD|March 20, 2022
Genitourinary and lower gastrointestinal conditions in patients with myotonic dystrophy type 1: A systematic review of evidence and implications for clinical practiceIsabelle Fisette-Paulhus, Cynthia Gagnon, Laura Girard-Côté, et al.
Neuromuscular Disorders : NMD|March 4, 2022
No effect of triheptanoin in patients with phosphofructokinase deficiencyDaniel Emil Raaschou-Pedersen, Karen Lindhardt Madsen, Nicoline Løkken, et al.
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