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Neuromuscular Disorders
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Volume 29, Issue 11
Pages 819-912 (November 2019)
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1. Editorial Board
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2. Malignancy and myositis, from molecular mimicry to tumor infiltrating lymphocytes
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Albert Selva-O'Callaghan, Javier Ros, Albert Gil-Vila, Gemma Vila-Pijoan, ... Iago Pinal-Fernandez
3. MYO-MRI diagnostic protocols in genetic myopathies
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Jodi Warman Chardon, Jordi Díaz-Manera, Giorgio Tasca, Carsten G. Bönnemann, ... Robert Y Carlier
4. Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study
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Darryl C. De Vivo, Enrico Bertini, Kathryn J. Swoboda, Wuh-Liang Hwu, ... Wildon Farwell
5. Longitudinal natural history in young boys with Duchenne muscular dystrophy
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Giorgia Coratti, Claudia Brogna, Giulia Norcia, Valeria Ricotti, ... Eugenio Mercuri
6. Large in-frame 5′ deletions in DMD associated with mild Duchenne muscular dystrophy: Two case reports and a review of the literature
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Elizabeth M. Gibbs, Florian Barthélémy, Emilie D. Douine, Natalie C. Hardiman, ... M. Carrie Miceli
7. A simple and rapid immunoassay predicts dysferlinopathies in peripheral blood film
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Daniel Cox, Matthew Henderson, Volker Straub, Rita Barresi
8. Measurement properties and utility of performance-based outcome measures of physical functioning in individuals with facioscapulohumeral dystrophy – A systematic review and evidence synthesis
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K. de Valle, J.L. McGinley, I. Woodcock, M.M. Ryan, F. Dobson
9. Fatigue in primary genetic mitochondrial disease: No rest for the weary
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Sumit Parikh, Rachel Galioto, Brittany Lapin, Richard Haas, ... Amel Karaa
10. Clinical features of Pompe disease with motor neuronopathy
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Li-Kai Tsai, Wuh-Liang Hwu, Ni-Chung Lee, Pei-Hsin Huang, Yin-Hsiu Chien
11. De novo variant in SCN4A causes neonatal sodium channel myotonia with general muscle stiffness and respiratory failure
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Astrid Pechmann, Matthias Eckenweiler, David Schorling, Dimitra Stavropoulou, ... Janbernd Kirschner
12. Predominant distal muscle involvement in spinal muscular atrophy
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C. Brogna, L. Cristiano, T. Verdolotti, L. Ficociello, ... E. Mercuri
