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Neuromuscular Disorders : NMD|March 1, 1997
A novel SOD1 mutation in an Austrian family with amyotrophic lateral sclerosisB Bereznai, A Winkler, G D Borasio, et al.Neuromuscular Disorders : NMD|October 1, 1996
Hypoosmotic shocks induce elevation of resting calcium level in Duchenne muscular dystrophy myotubes contracting in vitroN Imbert, C Vandebrouck, B Constantin, et al.Neuromuscular Disorders : NMD|January 1, 1996
Skeletal muscle sarcoplasmic reticulum phenotype in myotonic dystrophyE Damiani, C Angelini, M Pelosi, et al.Neuromuscular Disorders : NMD|January 1, 1996
Multifrequency bioelectric impedance measurements for predicting body water compartments in duchenne muscular dystrophyG Bedogni, L Merlini, A Ballestrazzi, et al.Neuromuscular Disorders : NMD|May 1, 1996
Nerve terminal sprouting in botulinum type-A treated mouse levator auris longus muscleP Juzans, J X Comella, J Molgo, et al.Neuromuscular Disorders : NMD|May 1, 1996
Reduction of serum IgG level and peripheral T-cell counts are correlated with CTG repeat lengths in myotonic dystrophy patientsA Nakamura, T Kojo, K Arahata, et al.Neuromuscular Disorders : NMD|February 21, 2006
A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosisPascal Laforêt, Pascale Richard, Mina Ait Said, et al.Neuromuscular Disorders : NMD|February 21, 2006
Diaphragmatic function in advanced Duchenne muscular dystrophyJennifer Beck, Jan Weinberg, Carl-Hugo Hamnegård, et al.Neuromuscular Disorders : NMD|February 21, 2006
Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1BGian Maria Fabrizi, Maria Pellegrini, Chiara Angiari, et al.Neuromuscular Disorders : NMD|January 24, 2006
BSCL2 mutations in two Dutch families with overlapping Silver syndrome-distal hereditary motor neuropathyBart P C van de Warrenburg, Hans Scheffer, Jeroen J J van Eijk, et al.Pageof 340