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Neuromuscular Disorders : NMD|October 24, 2006
AbetaPP-overexpression and proteasome inhibition increase alphaB-crystallin in cultured human muscle: relevance to inclusion-body myositisSlawomir Wojcik, W King Engel, Janis McFerrin, et al.
Neuromuscular Disorders : NMD|October 24, 2006
A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intoleranceJohannes A Mayr, Ali-Reza Moslemi, Holger Förster, et al.
Neuromuscular Disorders : NMD|October 24, 2006
Myotilin: a prominent marker of myofibrillar remodellingLena Carlsson, Ji-Guo Yu, Monica Moza, et al.
Neuromuscular Disorders : NMD|July 1, 2006
Dermatomyositis, lobar panniculitis and inflammatory myopathy with abundant macrophagesEmmanuel Carrera, Johannes-Alexander Lobrinus, Olivier Spertini, et al.
Neuromuscular Disorders : NMD|July 8, 2008
Exclusion of biglycan mutations in a cohort of patients with neuromuscular disordersRachel A Peat, Jozef Gécz, Justin R Fallon, et al.
Neuromuscular Disorders : NMD|July 26, 2008
MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patientsAlbena Todorova, Tihomir Todorov, Bilyana Georgieva, et al.
Neuromuscular Disorders : NMD|July 29, 2008
Expanded HSAN4 phenotype associated with two novel mutations in NTRK1Stefan Wieczorek, Jonas Bergström, Maria Sääf, et al.
Neuromuscular Disorders : NMD|June 1, 2007
Quantitative skeletal muscle ultrasound: diagnostic value in childhood neuromuscular diseaseS Pillen, A Verrips, N van Alfen, et al.
Neuromuscular Disorders : NMD|June 1, 2007
Sensitivity and specificity of qualitative muscle ultrasound in assessment of suspected neuromuscular disease in childhoodKnut Brockmann, Peter Becker, Gudrun Schreiber, et al.
Neuromuscular Disorders : NMD|May 30, 2007
Musk-antibody positive myasthenia gravis presenting with isolated neck extensor weaknessC Casasnovas, M Povedano, S Jaumà, et al.
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