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Neuromuscular Disorders
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Volume 29, Issue 7
Pages 487-568 (July 2019)
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1. Editorial Board
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2. Inflammation-induced fibrosis in skeletal muscle of female carriers of Duchenne muscular dystrophy
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Corinna Preuße, Arpad von Moers, Heike Kölbel, Debora Pehl, ... Werner Stenzel
3. Dilated cardiomyopathy and limb-girdle muscular dystrophy-dystroglycanopathy due to novel pathogenic variants in the DPM3 gene
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J. Svahn, P. Laforêt, C. Vial, N. Streichenberger, ... T. Stojkovic
4. Longitudinal study of upper extremity reachable workspace in fascioscapulohumeral muscular dystrophy
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Maya N. Hatch, Kiin Kim, Gregorij Kurillo, Alina Nicorici, ... Jay J. Han
5. European regulators’ views on a wearable-derived performance measurement of ambulation for Duchenne muscular dystrophy regulatory trials
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Marion Haberkamp, Jane Moseley, Dimitrios Athanasiou, Fernando de Andres-Trelles, ... Armando Magrelli
6. Salbutamol tolerability and efficacy in patients with spinal muscular atrophy type II
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A.L. Frongia, D. Natera-de Benito, C. Ortez, M. Alarcón, ... A. Nascimento
7. Evolution of bone mineral density, bone metabolism and fragility fractures in Spinal Muscular Atrophy (SMA) types 2 and 3
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Giovanni Baranello, Silvia Vai, Francesca Broggi, Riccardo Masson, ... Maria Luisa Bianchi
8. Efficient gene transfer into primary muscle cells to analyze nerve-independent postsynaptic organization in vitro
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Jessica Mella, Viviana Pérez, Diego Zelada, Nicolás Moreno, ... Juan Pablo Henríquez
9. Concurrent positive anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase antibody with reducing body myopathy: Possible double trouble
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Jantima Tanboon, Oranee Sanmaneechai, Sirirat Charuvanij, Tumtip Sangruchi, ... Ichizo Nishino
10. Novel compound heterozygous GFPT1 mutations in a family with limb-girdle myasthenia with tubular aggregates
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Hai-yang Luo, Lu Zhao, Cheng-yuan Mao, Zhi-hua Yang, ... Yu-ming Xu
11. Stopping oral steroid-sparing agents at initiation of rituximab in myasthenia gravis
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Ricardo H. Roda, Leana Doherty, Andrea M. Corse
12. The prevalence of faecal incontinence in myotonic dystrophy type 1
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R.K.H. Petty, M.P. Eugenicos, M.J. Hamilton, M.E. Farrugia, ... C. Longman
13. Rhabdomyolysis and myoglobinuria following bisphosphonate infusion in patients with Duchenne muscular dystrophy
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Jennifer Lemon, Lucy Turner, Poonam Dharmaraj, Stefan Spinty
