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Neuromuscular Disorders : NMD|November 18, 2005
The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient miceMaja von der Hagen, Steven H Laval, Lynsey M Cree, et al.
Neuromuscular Disorders : NMD|November 18, 2005
Major myofibrillar changes in early onset myopathy due to de novo heterozygous missense mutation in lamin A/C geneA D'Amico, S Benedetti, S Petrini, et al.
Neuromuscular Disorders : NMD|November 18, 2005
Co-segregation of LMNA and PMP22 gene mutations in the same familyElena Pegoraro, Bruno F Gavassini, Sara Benedetti, et al.
Neuromuscular Disorders : NMD|October 23, 2009
The difficulty in confirming clinical diagnosis of myasthenia gravis in a seronegative patient: a possible neurophysiological approachP Caliandro, A Evoli, E Stålberg, et al.
Neuromuscular Disorders : NMD|September 4, 2018
GsMTx4-D provides protection to the D2.mdx mouseChristopher W Ward, Frederick Sachs, Ernest D Bush, et al.
Neuromuscular Disorders : NMD|August 29, 2018
New variant of necklace fibres display peculiar lysosomal structures and mitophagyJan Leo Rinnenthal, Carsten Dittmayer, Kerstin Irlbacher, et al.
Neuromuscular Disorders : NMD|September 6, 2016
Quantifying disease activity in fatty-infiltrated skeletal muscle by IDEAL-CPMG in Duchenne muscular dystrophyAmi Mankodi, Courtney A Bishop, Sungyoung Auh, et al.
Neuromuscular Disorders : NMD|May 13, 2017
HLA and age of onset in myasthenia gravisErnestina Santos, Andreia Bettencourt, Ana Martins da Silva, et al.
Neuromuscular Disorders : NMD|June 12, 2017
Deletion of P2 promoter of GJB1 gene a cause of Charcot-Marie-Tooth diseaseR Kulshrestha, S Burton-Jones, T Antoniadi, et al.
Neuromuscular Disorders : NMD|November 13, 2009
Myelin protein zero Val102fs mutation manifesting with isolated spinal root hypertrophyCorrado Marchini, Sandro Zambito Marsala, Matteo Bendini, et al.
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