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Human Molecular Genetics|April 1, 1995
Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophyN R Rodrigues, N Owen, K Talbot, et al.Muscle & Nerve|September 1, 1979
Chloroquine-induced cytosomes with curvilinear profiles in muscleH E Neville, C A Maunder-Sewry, J McDougall, et al.Neuropediatrics|February 1, 1995
Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin statusE Mercuri, F Muntoni, A Berardinelli, et al.Journal of Cell Science|March 1, 1985
A novel procedure for pattern analysis of features present on freeze-fractured plasma membranesS T Appleyard, J A Witkowski, B D Ripley, et al.Developmental Medicine and Child Neurology|June 1, 1985
Chromosome 15 in Prader-Willi syndromeC N Fear, D E Mutton, A C Berry, et al.Pediatrics|September 1, 1988
Predictive value of early continuous electroencephalogram monitoring in ventilated preterm infants with intraventricular hemorrhageJ Connell, L de Vries, R Oozeer, et al.The Journal of Pediatrics|August 4, 1999
Optimality score for the neurologic examination of the infant at 12 and 18 months of ageL Haataja, E Mercuri, R Regev, et al.Neuromuscular Disorders : NMD|July 1, 1995
Expression of laminin subunits in congenital muscular dystrophyC A Sewry, J Philpot, D Mahony, et al.Society of General Physiologists Series|January 1, 1995
In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4J Wang, V Dubowitz, F Lehmann-Horn, et al.Neuromuscular Disorders : NMD|August 26, 1998
Fifty year follow-up of a patient with central core disease shows slow but definite progressionP J Lamont, V Dubowitz, D N Landon, et al.Pageof 24