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Neuromuscular Disorders : NMD|October 16, 2004
Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathyLuca Passamonti, Maria Muglia, Angela Magariello, et al.
Neuromuscular Disorders : NMD|October 16, 2004
Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNASer(UCN) geneVincenza Fetoni, Egill Briem, Franco Carrara, et al.
Neuromuscular Disorders : NMD|October 16, 2004
Characteristics of the increase in plasma brain natriuretic peptide level in left ventricular systolic dysfunction, associated with muscular dystrophy in comparison with idiopathic dilated cardiomyopathyJun Demachi, Yutaka Kagaya, Jun Watanabe, et al.
Neuromuscular Disorders : NMD|October 16, 2004
A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndromeJuliane S Müller, Angela Abicht, Hans-Jürgen Christen, et al.
Neuromuscular Disorders : NMD|March 29, 2005
Temperament and character in patients with classical myotonic dystrophy type 1 (DM-1)S Winblad, C Lindberg, S Hansen
Neuromuscular Disorders : NMD|March 29, 2005
A novel ANT1 gene mutation with probable germline mosaicism in autosomal dominant progressive external ophthalmoplegiaMarcus Deschauer, Gavin Hudson, Tobias Müller, et al.
Neuromuscular Disorders : NMD|February 8, 2005
Sarcoplasmic masses in equine skeletal muscleM Aleman, R A Lecouteur, J E Nieto, et al.
Neuromuscular Disorders : NMD|September 8, 2004
The congenital muscular dystrophies in 2004: a century of exciting progressFrancesco Muntoni, Thomas Voit
Neuromuscular Disorders : NMD|September 8, 2004
Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) geneB J C van den Bosch, I F M de Coo, A T M Hendrickx, et al.
Neuromuscular Disorders : NMD|September 8, 2004
Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic AtaxiaM Kinali, H Jungbluth, L H Eunson, et al.
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