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Neurology|February 26, 2003
CMT with pyramidal features. Charcot-Marie-ToothS Vucic, M Kennerson, D Zhu, et al.Journal of the Neurological Sciences|December 1, 1985
The creatine kinase reference interval. An assessment of intra- and inter-individual variationG A Nicholson, G Morgan, M Meerkin, et al.American Journal of Medical Genetics|December 18, 1998
Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetusS Rudnik-Schöneborn, G A Nicholson, G Morgan, et al.Neurology|February 9, 2005
Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth lociA Kochanski, M Kennerson, M Kawulak, et al.Annals of the New York Academy of Sciences|December 10, 1999
Mutation testing in Charcot-Marie-Tooth neuropathyG A NicholsonNeurology|April 1, 1991
Penetrance of the hereditary motor and sensory neuropathy Ia mutation: assessment by nerve conduction studiesG A NicholsonJournal of the Neurological Sciences|October 1, 1982
Decreased A23187-induced chemiluminescence in Duchenne muscular dystrophy granulocytesG A Nicholson, J SugarsJournal of the Neurological Sciences|March 1, 1982
An evaluation of lymphocyte capping in Duchenne muscular dystrophyG A Nicholson, J SugarsJournal of the Neurological Sciences|July 1, 1981
Plasma creatine kinase isoenzymes in the Bar harbor dystrophic mouseG A Nicholson, E MathesonJournal of Motor Behavior|January 1, 1979
Sequential predictability effects on initiation time and movement time for adults and childrenB KerrPageof 296