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Neuromuscular Disorders : NMD|September 7, 2020
Gain and loss of abilities in type II SMA: A 12-month natural history studyGiorgia Coratti, Simona Lucibello, Maria C Pera, et al.
Neuromuscular Disorders : NMD|February 15, 2020
Myasthenia gravis after etanercept and ustekinumab treatment for psoriatic arthritis: A case reportGiulia Nicocia, Carmen Bonanno, Antonino Lupica, et al.
Neuromuscular Disorders : NMD|February 15, 2020
A cross-sectional study of hand function in inclusion body myositis: Implications for functional rating scaleAva Yun Lin, Maggie Clapp, Elizabeth Karanja, et al.
Neuromuscular Disorders : NMD|December 10, 2019
Long-term data with idebenone on respiratory function outcomes in patients with Duchenne muscular dystrophyLaurent Servais, Chiara S M Straathof, Ulrike Schara, et al.
Neuromuscular Disorders : NMD|August 15, 2017
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunctionMaria Carmela Pera, Marco Luigetti, Marika Pane, et al.
Neuromuscular Disorders : NMD|August 16, 2017
A comparative study of care practices for young boys with Duchenne muscular dystrophy between Japan and European countries: Implications of early diagnosisFumi Takeuchi, Hirofumi Komaki, Zentaro Yamagata, et al.
Neuromuscular Disorders : NMD|August 19, 2017
Three novel recessive mutations in LAMA2, SYNE1, and TTN are identified in a single case with congenital muscular dystrophyLiang Wu, Bingwu Xiang, Huan Zhang, et al.
Neuromuscular Disorders : NMD|March 27, 2018
Parental mosaicism in RYR1-related Central Core DiseaseS Marks, E van Ruitenbeek, P Fallon, et al.
Neuromuscular Disorders : NMD|January 26, 2019
Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin geneKirsi J Kiiski, Vilma-Lotta Lehtokari, Anna K Vihola, et al.
Neuromuscular Disorders : NMD|January 20, 2019
Dropped head syndrome as a manifestation of Charcot-Marie-Tooth disease type 4CCamila Maria de Oliveira, Helena Fussiger, Pablo Brea Winckler, et al.
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