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Neuromuscular Disorders : NMD|May 1, 1995
Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophyJ Philpot, H Topaloglu, J Pennock, et al.Archives of Disease in Childhood|May 1, 1995
Duchenne muscular dystrophy presenting with failure to thriveR Rapisarda, F Muntoni, P Gobbi, et al.Archives of Disease in Childhood|February 1, 1989
Congenital myotonic dystrophy: respiratory function at birth determines survivalM A Rutherford, J Z Heckmatt, V DubowitzJournal of the Neurological Sciences|November 1, 1990
Nature of the mononuclear infiltrate and the mechanism of muscle damage in juvenile dermatomyositis and Duchenne muscular dystrophyR M McDouall, M J Dunn, V DubowitzThe Biochemical Journal|March 1, 1982
Erythrocyte-ghost Ca2+-stimulated Mg2+-dependent adenosine triphosphatase in Duchenne muscular dystrophyM J Dunn, A H Burghes, V DubowitzClinical and Experimental Rheumatology|January 1, 1989
A comparative study of in vitro proliferative responses to mitogens and immunoglobulin production in patients with inflammatory muscle diseaseG Cambridge, A Faith, C Saunders, et al.Journal of the Neurological Sciences|July 1, 1985
Lobulated fibers in neuromuscular diseasesM J Guerard, C A Sewry, V DubowitzNeuromuscular Disorders : NMD|July 1, 1995
Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscleJ Philpot, C Sewry, J Pennock, et al.Neuromuscular Disorders : NMD|January 1, 1995
Congenital symmetrical weakness of the upper limbs resembling brachial plexus palsy: a possible sequel of drug toxicity in first trimester of pregnancy?J Philpot, F Muntoni, S Skellett, et al.Journal of the Neurological Sciences|May 1, 1980
Erythrocyte ghost Na+,K+-adenosine triphosphatase in Duchenne muscular dystrophyM J Dunn, A H Burghes, V DubowitzPageof 24