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Muscle & Nerve|November 3, 2009
Homozygosity for dominant mutations increases severity of muscle channelopathiesMarianne Arzel-Hézode, Damien Sternberg, Nacira Tabti, et al.Muscle & Nerve|November 3, 2009
Tibialis anterior branch involvement in fibular intraneural gangliaMarie-Noëlle Hébert-Blouin, Kimberly K Amrami, Huan Wang, et al.Muscle & Nerve|November 3, 2009
Kinetics of neuromuscular changes during low-frequency electrical stimulationMaria Papaiordanidou, David Guiraud, Alain VarrayMuscle & Nerve|November 11, 2005
Electromyographic studies in mdx and wild-type C57 miceJay J Han, Gregory T Carter, Jennifer J Ra, et al.Muscle & Nerve|November 11, 2005
An alternative test of electromyographic normalization in patientsWei-Li Hsu, Vijaya Krishnamoorthy, John Peter ScholzMuscle & Nerve|October 18, 2005
Morphological effects of myasthenia gravis patient sera on human muscle cellsSteven Paul Luckman, Geir Olve Skeie, Geir Helgeland, et al.Muscle & Nerve|October 18, 2005
The role of neurotrophins in muscle under physiological and pathological conditionsGuillaume Chevrel, Reinhard Hohlfeld, Michael SendtnerMuscle & Nerve|January 1, 1978
Autosomal dominant "spheroid body myopathy"H H Goebel, J Muller, H W Gillen, et al.Muscle & Nerve|March 1, 1978
Becker-type muscular dystrophyW G Bradley, M Z Jones, J M Mussini, et al.Muscle & Nerve|March 1, 1978
Neonatal experimental autoimmune myasthenia gravisD B Sanders, E E Cobb, J B WinfieldPageof 893