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Neuromuscular Disorders : NMD|September 14, 2011
Autoimmune myasthenia gravis, immunotherapy and thymectomy in childrenTyson L Ware, Monique M Ryan, Andrew J Kornberg
Neuromuscular Disorders : NMD|December 14, 2011
Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophyChien-Hua Wang, Mana Leung, Wen-Chen Liang, et al.
Neuromuscular Disorders : NMD|February 3, 2012
Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathyYoung-Eun Park, Hyang-Sook Kim, Chang-Hoon Lee, et al.
Neuromuscular Disorders : NMD|September 24, 2011
Clinical features in a series of fast channel congenital myasthenia syndromeJacqueline Palace, Daniel Lashley, Stephen Bailey, et al.
Neuromuscular Disorders : NMD|October 1, 2011
Muscle glycogen storage disease 0 presenting recurrent syncope with weakness and myalgiaSayuri Sukigara, Wen-Chen Liang, Hirofumi Komaki, et al.
Neuromuscular Disorders : NMD|January 14, 2012
A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvementAyako Hattori, Hirofumi Komaki, Masao Kawatani, et al.
Neuromuscular Disorders : NMD|February 1, 2012
Cerebral and muscle MRI abnormalities in myotonic dystrophyDaniel T Franc, Ryan L Muetzel, Paul R Robinson, et al.
Neuromuscular Disorders : NMD|January 24, 2012
Exome sequencing identifies KIAA1377 and C5orf42 as susceptibility genes for monomelic amyotrophyYoung-Min Lim, Insong Koh, Young-Mi Park, et al.
Neuromuscular Disorders : NMD|December 27, 2011
A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest ponyInge D Wijnberg, Marta Owczarek-Lipska, Roberta Sacchetto, et al.
Neuromuscular Disorders : NMD|December 27, 2011
Acid phosphatase-positive globular inclusions is a good diagnostic marker for two patients with adult-onset Pompe disease lacking disease specific pathologyRie S Tsuburaya, Kazunari Monma, Yasushi Oya, et al.
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