Showing results (1261-1270 of 3,399) with videos related to

Sort By:
Pageof 340
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.
Neuromuscular Disorders : NMD|January 26, 2007
Distribution of glucocorticoid receptor alpha and beta subtypes in the idiopathic inflammatory myopathiesJan L De Bleecker, Boel De Paepe, Veerle L Vervaet, et al.
Neuromuscular Disorders : NMD|April 17, 2007
Cap disease caused by heterozygous deletion of the beta-tropomyosin gene TPM2Vilma-Lotta Lehtokari, Chantal Ceuterick-de Groote, Peter de Jonghe, et al.
Neuromuscular Disorders : NMD|April 10, 2007
Phenotypic patterns of desminopathy associated with three novel mutations in the desmin geneMontse Olivé, Judith Armstrong, Francesc Miralles, et al.
Pageof 340